100 lavori in ThermoFisher Scientific
Senior CTM - Neuroscience
Remota
ThermoFisher Scientific
Oggi
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Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join us as a Senior Clinical Team Manager - Make an Impact at the Forefront of Innovation.
The Senior Clinical Team Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. The Senior Clinical Team Manager interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. The position involves working on projects of low to moderate complexity and as part of a team of CTMs.
**We are looking for an experienced CTM to join our Neuroscience team. We are looking for candidates with extensive experience in the following indications:**
+ **Ophthalmology: General ophthalmology, Diabetic Macular Edema & Geographic Atrophy**
+ **Rare Disease: : Myasthenia Gravis, Huntington's, ALS, DMD, CIDP, DM1 (myotonic dystrophy) and FSHD - CAR-T experience a plus**
+ **Sleep, Epilepsy, and/or Psychiatry (Depression & Schizophrenia)**
What You'll Do:
- Manage all clinical operational and quality aspects of allocated studies, of high complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
- Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
- May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
- May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed. Ensure that essential document quality meets the expectation of Regulatory Compliance Review. Review and follows up on all questions raised by the ethics committees.
- May provide input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.
Education & Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities:
- Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams
- Good planning and organizational skills to enable effective prioritization of workload
- Solid interpersonal and problem solving skills to enable working in a multicultural matrix organization
- Capable of working effectively in a changing environment with complex/ambiguous situations
- Familiarity with the practices, processes, and requirements of clinical monitoring
- Good judgment and decision making skills
- Effective oral and written communication skills, including English language proficiency
- Capable of evaluating workload against project budget and adjusting resources accordingly
- Sound financial acument and knowledge of budgeting, forecasting and fiscal management
- Strong attention to detail
- Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
- Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Working Conditions and Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Frequently drives to site locations and frequently travels both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join us as a Senior Clinical Team Manager - Make an Impact at the Forefront of Innovation.
The Senior Clinical Team Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. The Senior Clinical Team Manager interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. The position involves working on projects of low to moderate complexity and as part of a team of CTMs.
**We are looking for an experienced CTM to join our Neuroscience team. We are looking for candidates with extensive experience in the following indications:**
+ **Ophthalmology: General ophthalmology, Diabetic Macular Edema & Geographic Atrophy**
+ **Rare Disease: : Myasthenia Gravis, Huntington's, ALS, DMD, CIDP, DM1 (myotonic dystrophy) and FSHD - CAR-T experience a plus**
+ **Sleep, Epilepsy, and/or Psychiatry (Depression & Schizophrenia)**
What You'll Do:
- Manage all clinical operational and quality aspects of allocated studies, of high complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
- Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
- May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
- May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed. Ensure that essential document quality meets the expectation of Regulatory Compliance Review. Review and follows up on all questions raised by the ethics committees.
- May provide input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.
Education & Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities:
- Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams
- Good planning and organizational skills to enable effective prioritization of workload
- Solid interpersonal and problem solving skills to enable working in a multicultural matrix organization
- Capable of working effectively in a changing environment with complex/ambiguous situations
- Familiarity with the practices, processes, and requirements of clinical monitoring
- Good judgment and decision making skills
- Effective oral and written communication skills, including English language proficiency
- Capable of evaluating workload against project budget and adjusting resources accordingly
- Sound financial acument and knowledge of budgeting, forecasting and fiscal management
- Strong attention to detail
- Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
- Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Working Conditions and Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Frequently drives to site locations and frequently travels both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Regional System Specialist
Remota
ThermoFisher Scientific
Oggi
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Descrizione Del Lavoro
**Work Schedule**
**Environmental Conditions**
**Job Description**
**Position Summary:**
Be one of our field experts, providing specialized service and support on the installation, integration, servicing, repair and troubleshooting of PDX systems portfolio, leveraging product knowledge and technical competency to enable our customers to improve multiple myeloma patient outcomes.
**A day in the life:**
+ Be part of a multidisciplinary global team that enables our customers to successfully complete their important clinical work on the EXENT® ProteinHub® and Optilite® systems.
+ The Regional System Specialist will ensure successful installation, system integration, validation, scheduled maintenance, upgrades, troubleshooting and repair of the EXENT® system - MALDI TOF Mass Spec, automated MALDI plate preparation and associated software, integrating expertise on ProteinHub® and Optilite® systems.
+ The role also involves provision of timely technical support to customers and colleagues including remote access support and cross-functional technical investigation work - efficiently diagnosing faults and restoring full system functionality.
+ As an expert in their field, the System Specialist must be confident in participating in technical discussions on the product - both hardware and software.
+ Perform scheduled preventative maintenance (PM) visits within the timeframes required.
+ Complete service reports in Service CRM and ensure they are completed both fully and accurately.
+ Maintain accurate records of spare parts, ensuring parts are used appropriately and support with spare part stock checks and reconciliation.
+ Update instruments placed at customer laboratories with software and data management upgrades as required.
+ Provide feedback to global product teams on instrument reliability and quality.
+ Whilst the role will primarily focus on the support of the EXENT® solution. You will also be required to cross train on other Binding Site products such as Optilte®/ ProteinHub® to support the local commercial organisation.
+ The role will require travel across Italy with the potential to travel internationally to support the wider EXENT Specialist Team, sometimes at short notice for up-to two weeks at a time.
Keys to Success:
**Education**
+ Qualification in a mechanical, electrical or life science discipline or relevant experience.
**Experience**
+ Experience in a scientific or engineering discipline. (eg. Clinical / research laboratories / electronics / biotechnology / medical devices)
+ Desirable: experience servicing/maintaining mass spectrometry and/or automated sample preparation systems.
**Knowledge, Skills, Abilities**
+ Mass spectrometry and/or automated sample preparation knowledge is highly desirable.
+ Strong technical aptitude and problem-solving skills.
+ Customer-focused with good communication skills
+ Fluency in English - both written and verbal.
+ Ability to travel locally and internationally at short notice
+ Desirable: Previous experience in servicing analytical equipment or equivalent applications specialist/product support experience
**Physical Requirements / Work Environment**
This position will require working in a wide variety of clinical/hospital laboratories.
Technical training may be required periodically at the UK head office.
Join Thermo Fisher Scientific Inc. today and be part of a diverse and inclusive community dedicated to making the world healthier, cleaner, and safer. As an equal opportunity employer, we value individuals with diverse experiences, backgrounds, and perspectives. We are committed to providing reasonable accommodation for individuals with disabilities throughout the recruitment process. Please contact us to request accommodation and start your journey with us.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Environmental Conditions**
**Job Description**
**Position Summary:**
Be one of our field experts, providing specialized service and support on the installation, integration, servicing, repair and troubleshooting of PDX systems portfolio, leveraging product knowledge and technical competency to enable our customers to improve multiple myeloma patient outcomes.
**A day in the life:**
+ Be part of a multidisciplinary global team that enables our customers to successfully complete their important clinical work on the EXENT® ProteinHub® and Optilite® systems.
+ The Regional System Specialist will ensure successful installation, system integration, validation, scheduled maintenance, upgrades, troubleshooting and repair of the EXENT® system - MALDI TOF Mass Spec, automated MALDI plate preparation and associated software, integrating expertise on ProteinHub® and Optilite® systems.
+ The role also involves provision of timely technical support to customers and colleagues including remote access support and cross-functional technical investigation work - efficiently diagnosing faults and restoring full system functionality.
+ As an expert in their field, the System Specialist must be confident in participating in technical discussions on the product - both hardware and software.
+ Perform scheduled preventative maintenance (PM) visits within the timeframes required.
+ Complete service reports in Service CRM and ensure they are completed both fully and accurately.
+ Maintain accurate records of spare parts, ensuring parts are used appropriately and support with spare part stock checks and reconciliation.
+ Update instruments placed at customer laboratories with software and data management upgrades as required.
+ Provide feedback to global product teams on instrument reliability and quality.
+ Whilst the role will primarily focus on the support of the EXENT® solution. You will also be required to cross train on other Binding Site products such as Optilte®/ ProteinHub® to support the local commercial organisation.
+ The role will require travel across Italy with the potential to travel internationally to support the wider EXENT Specialist Team, sometimes at short notice for up-to two weeks at a time.
Keys to Success:
**Education**
+ Qualification in a mechanical, electrical or life science discipline or relevant experience.
**Experience**
+ Experience in a scientific or engineering discipline. (eg. Clinical / research laboratories / electronics / biotechnology / medical devices)
+ Desirable: experience servicing/maintaining mass spectrometry and/or automated sample preparation systems.
**Knowledge, Skills, Abilities**
+ Mass spectrometry and/or automated sample preparation knowledge is highly desirable.
+ Strong technical aptitude and problem-solving skills.
+ Customer-focused with good communication skills
+ Fluency in English - both written and verbal.
+ Ability to travel locally and internationally at short notice
+ Desirable: Previous experience in servicing analytical equipment or equivalent applications specialist/product support experience
**Physical Requirements / Work Environment**
This position will require working in a wide variety of clinical/hospital laboratories.
Technical training may be required periodically at the UK head office.
Join Thermo Fisher Scientific Inc. today and be part of a diverse and inclusive community dedicated to making the world healthier, cleaner, and safer. As an equal opportunity employer, we value individuals with diverse experiences, backgrounds, and perspectives. We are committed to providing reasonable accommodation for individuals with disabilities throughout the recruitment process. Please contact us to request accommodation and start your journey with us.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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1
Inside Sales Representative - Technical Sales Specialist Italy for Molecular Biology & Sample Prep
milan
ThermoFisher Scientific
Oggi
Lavoro visualizzato
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**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
This is an ideal opportunity for someone that wants to start their career in sales or is looking to develop further within our exciting industry! We are looking for someone who has a curiosity about science, practical lab experience and has proven a sales agility, but may lack sales experience in the Life Sciences industry. The candidate will be responsible for developing sales within a defined territory (Italy), focusing on the Molecular Biology and Sample Prep portfolios.
**DESCRIPTION**
How you will make an impact:
The successful candidate will use product features and benefits to identify and qualify leads, initiate the sales process, and effectively promote the Company's products and services to exceed the assigned territory sales plan. The primary objective of the position is to build positive relationships with customers virtually to achieve sales.
What you will do:
+ Develop strong, consultative relationships with customers and channel partners within the assigned territory, focusing on customer happiness, revenue and margin growth.
+ Coordinate the entire sales process for assigned accounts and products.
+ Develop a deep technical knowledge of assigned products within the portfolio of responsibility, as well as strong solid understanding of the features and benefits of competition's products.
+ Champion use of Salesforce (CRM) for accurate territory management.
+ Responsible for achieving or exceeding the sales plan by maintaining existing business and developing new relationships.
+ Ensure local/country business requirement are met whilst also aligning with business unit goals and objectives.
**REQUIREMENTS**
How you will get here:
Minimum Qualifications:
+ Master's Degree plus 2 years of sales and/or laboratory/research experience.
+ Proficient in Italian and English written and oral.
+ Previous laboratory experience preferred.
+ Previous sales/inside sales experience preferred.
+ General knowledge of product portfolio.
Essential Skills:
+ Excellent time management and prioritization skills.
+ Application of problem-solving and multi-tasking techniques.
+ Ability to develop technical knowledge across a broad range of complex products.
+ Solid understanding and application of MS Office.
+ Strong verbal and written communication, and presentation skills.
+ Proven record of delivering excellent customer service.
+ Outstanding interpersonal skills.
+ Possess excellent eye for business!
+ Demonstrates the Thermo Fisher values (The Four I's) - Integrity, Intensity, Innovation, and Involvement.
Travel requirements: Ability to travel within territory up to 20% of the time.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
This is an ideal opportunity for someone that wants to start their career in sales or is looking to develop further within our exciting industry! We are looking for someone who has a curiosity about science, practical lab experience and has proven a sales agility, but may lack sales experience in the Life Sciences industry. The candidate will be responsible for developing sales within a defined territory (Italy), focusing on the Molecular Biology and Sample Prep portfolios.
**DESCRIPTION**
How you will make an impact:
The successful candidate will use product features and benefits to identify and qualify leads, initiate the sales process, and effectively promote the Company's products and services to exceed the assigned territory sales plan. The primary objective of the position is to build positive relationships with customers virtually to achieve sales.
What you will do:
+ Develop strong, consultative relationships with customers and channel partners within the assigned territory, focusing on customer happiness, revenue and margin growth.
+ Coordinate the entire sales process for assigned accounts and products.
+ Develop a deep technical knowledge of assigned products within the portfolio of responsibility, as well as strong solid understanding of the features and benefits of competition's products.
+ Champion use of Salesforce (CRM) for accurate territory management.
+ Responsible for achieving or exceeding the sales plan by maintaining existing business and developing new relationships.
+ Ensure local/country business requirement are met whilst also aligning with business unit goals and objectives.
**REQUIREMENTS**
How you will get here:
Minimum Qualifications:
+ Master's Degree plus 2 years of sales and/or laboratory/research experience.
+ Proficient in Italian and English written and oral.
+ Previous laboratory experience preferred.
+ Previous sales/inside sales experience preferred.
+ General knowledge of product portfolio.
Essential Skills:
+ Excellent time management and prioritization skills.
+ Application of problem-solving and multi-tasking techniques.
+ Ability to develop technical knowledge across a broad range of complex products.
+ Solid understanding and application of MS Office.
+ Strong verbal and written communication, and presentation skills.
+ Proven record of delivering excellent customer service.
+ Outstanding interpersonal skills.
+ Possess excellent eye for business!
+ Demonstrates the Thermo Fisher values (The Four I's) - Integrity, Intensity, Innovation, and Involvement.
Travel requirements: Ability to travel within territory up to 20% of the time.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
2
QC Microbiological Laboratory Supervisor
ThermoFisher Scientific
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Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, including protecting the environment, ensuring our food is safe, and helping to find cures for cancer.
**DESCRIPTION**
**How will you make an impact?**
As QC Microbiological Laboratory Supervisor, you will lead and coordinate Microbiological Quality Control laboratory activities by effectively planning, organizing, and monitoring analytical operations to ensure on-time delivery, Right First Time (RFT) performance, regulatory compliance, and customer satisfaction.
**What will you do?**
+ Ensure the effective management of the Microbiological Quality Control laboratory by leading, coordinating, and developing the assigned team to perform all required microbiological testing in compliance with safety regulations, approved methods, applicable regulatory requirements (EU GMP, US GMP, FDA regulations, and other relevant national regulations), marketing authorization dossier requirements, and company quality standards.
+ Provide technical leadership and oversight for laboratory operations supporting pharmaceutical manufacturing, from raw material and incoming material testing through finished product release and stability studies.
+ Support the Quality Department in the preparation for and execution of client and regulatory authority audits and inspections (e.g., FDA, EMA, AIFA,) by coordinating cross-functional activities, managing audit readiness, and ensuring the timely availability of required documentation and responses.
+ Draft and review analytical specifications, study protocols, reports, analytical methods, and Standard Operating Procedures (SOPs) in compliance with applicable national and international GMP regulations and company quality standards.
+ Participate in customer meetings and conference calls to discuss technical topics within your area of expertise.
+ Lead laboratory investigations, including Out-of-Specification (OOS) results, deviations, Out-of-Trend (OOT) results, and the definition and implementation of appropriate corrective and preventive actions (CAPAs).
+ Oversee Method Development, Method Validation, and Method Transfer activities for assigned projects, as applicable.
+ Collaborate with the Manager to define and monitor the department budget and CAPEX, ensuring the efficient management of the Microbiological QC laboratory.
+ Drive operational excellence by mentoring team members, optimizing laboratory workflows, implementing continuous improvement initiatives, and promoting Lean and Practical Process Improvement (PPI) principles while maintaining the highest quality standards.
+ Lead, coach, and develop the assigned team by setting objectives, monitoring performance, recognizing achievements, and identifying training and development needs to build a high-performing, engaged, and accountable organization.
**REQUIREMENTS**
+ Bachelor's degree or higher in Biology, Microbiology, Biochemistry, Pharmaceutical Chemistry and Technology (CTF), or a related scientific discipline.
+ Multiple years of experience in Microbiological Quality Control within the pharmaceutical and/or biotechnology industry.
+ At least 3 years of experience in a people leadership role managing laboratory operations, including scheduling, resource planning, and process improvement initiatives.
+ Experience in pharmaceutical manufacturing, preferably in an aseptic environment.
+ Strong knowledge of cGMP, FDA regulations, EU GMP, ICH guidelines, and pharmaceutical quality systems.
+ Strong knowledge of Quality Risk Management principles, risk assessment methodologies, and Root Cause Analysis tools.
+ Strong understanding of ALCOA+ Data Integrity principles and regulatory expectations.
+ Excellent technical writing skills, including experience drafting SOPs, investigations, analytical methods, protocols, reports, and regulatory documentation.
+ Demonstrated leadership, problem-solving, and team management skills.
+ Excellent interpersonal and communication skills, with the ability to effectively interact with stakeholders at all organizational levels.
+ Proficiency in managing conflicting priorities, while working under time constraints, and in a dynamic team environment.
+ Proficiency with Microsoft Office applications, Laboratory Information Management Systems (LIMS), and electronic Quality Management Systems (eQMS).
+ Professional certifications in Quality Systems, Regulatory Compliance, Lean Six Sigma, or Project Management are considered an advantage.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, including protecting the environment, ensuring our food is safe, and helping to find cures for cancer.
**DESCRIPTION**
**How will you make an impact?**
As QC Microbiological Laboratory Supervisor, you will lead and coordinate Microbiological Quality Control laboratory activities by effectively planning, organizing, and monitoring analytical operations to ensure on-time delivery, Right First Time (RFT) performance, regulatory compliance, and customer satisfaction.
**What will you do?**
+ Ensure the effective management of the Microbiological Quality Control laboratory by leading, coordinating, and developing the assigned team to perform all required microbiological testing in compliance with safety regulations, approved methods, applicable regulatory requirements (EU GMP, US GMP, FDA regulations, and other relevant national regulations), marketing authorization dossier requirements, and company quality standards.
+ Provide technical leadership and oversight for laboratory operations supporting pharmaceutical manufacturing, from raw material and incoming material testing through finished product release and stability studies.
+ Support the Quality Department in the preparation for and execution of client and regulatory authority audits and inspections (e.g., FDA, EMA, AIFA,) by coordinating cross-functional activities, managing audit readiness, and ensuring the timely availability of required documentation and responses.
+ Draft and review analytical specifications, study protocols, reports, analytical methods, and Standard Operating Procedures (SOPs) in compliance with applicable national and international GMP regulations and company quality standards.
+ Participate in customer meetings and conference calls to discuss technical topics within your area of expertise.
+ Lead laboratory investigations, including Out-of-Specification (OOS) results, deviations, Out-of-Trend (OOT) results, and the definition and implementation of appropriate corrective and preventive actions (CAPAs).
+ Oversee Method Development, Method Validation, and Method Transfer activities for assigned projects, as applicable.
+ Collaborate with the Manager to define and monitor the department budget and CAPEX, ensuring the efficient management of the Microbiological QC laboratory.
+ Drive operational excellence by mentoring team members, optimizing laboratory workflows, implementing continuous improvement initiatives, and promoting Lean and Practical Process Improvement (PPI) principles while maintaining the highest quality standards.
+ Lead, coach, and develop the assigned team by setting objectives, monitoring performance, recognizing achievements, and identifying training and development needs to build a high-performing, engaged, and accountable organization.
**REQUIREMENTS**
+ Bachelor's degree or higher in Biology, Microbiology, Biochemistry, Pharmaceutical Chemistry and Technology (CTF), or a related scientific discipline.
+ Multiple years of experience in Microbiological Quality Control within the pharmaceutical and/or biotechnology industry.
+ At least 3 years of experience in a people leadership role managing laboratory operations, including scheduling, resource planning, and process improvement initiatives.
+ Experience in pharmaceutical manufacturing, preferably in an aseptic environment.
+ Strong knowledge of cGMP, FDA regulations, EU GMP, ICH guidelines, and pharmaceutical quality systems.
+ Strong knowledge of Quality Risk Management principles, risk assessment methodologies, and Root Cause Analysis tools.
+ Strong understanding of ALCOA+ Data Integrity principles and regulatory expectations.
+ Excellent technical writing skills, including experience drafting SOPs, investigations, analytical methods, protocols, reports, and regulatory documentation.
+ Demonstrated leadership, problem-solving, and team management skills.
+ Excellent interpersonal and communication skills, with the ability to effectively interact with stakeholders at all organizational levels.
+ Proficiency in managing conflicting priorities, while working under time constraints, and in a dynamic team environment.
+ Proficiency with Microsoft Office applications, Laboratory Information Management Systems (LIMS), and electronic Quality Management Systems (eQMS).
+ Professional certifications in Quality Systems, Regulatory Compliance, Lean Six Sigma, or Project Management are considered an advantage.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
3
Finance Controller
ThermoFisher Scientific
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**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, our Finance teams are important to our business and functional teams to make educated, sound decisions that drive our Mission and make us a stable and trusted industry leader. From Financial Planning & Analysis, Tax, Treasury, Financial Reporting, Audit, Investor Relations, Strategy & Corporate Development to Accounting, our Finance functions have a diverse and global presence, providing significant opportunities to develop outstanding career experiences and perspectives.
**How you will make an impact:**
The Italian Subsidiary of the Protein Diagnostics Division of Thermo Fisher, offers medical devices to all the Italian main Hospitals.
If you have a passion for financial accuracy and timeliness across a global, multi-faceted organization, Thermo Fisher Scientific's Accounting and Controllership function is the team for you. With a keen understanding of laws, regulations and compliance as well as reporting requirements consistent with ITA GAAP, this team uses innovative financial systems and controls, data security and robust processes to protect the company's assets and support its short- and long-term growth on a global scale. From technical accounting to budgeting and forecasting to planning and reporting, you will build relationships with internal and external audit teams as well as key business partners to drive sophisticated business decisions. You will have an opportunity to build strong organizational alliances to understand and mitigate risk, as well as capture opportunities and provide valuable support to all business partners.
Seeking a **proficient finance team member** who will provide finance, accounting and compliance to the Italian business. The successful candidate will implement accounting, controls and compliance procedures to ensure timely and accurate financial reporting. In addition, the position holder will identify and recommend operational improvement opportunities, and support leadership in achieving of business objectives.
**What you will do** :
+ Monthly and year end accounting vouchers, closing activities including journal entries, accruals, reporting and analysis;
+ Management of monthly VAT registers, VAT quarterly declaration data (LIPE), and VAT annual declaration data;
+ Fixed Assets monthly updates, depreciation and scrapping;
+ Analysis of customers collections for the bank update and the monthly collections report;
+ Balance Sheet Reconciliations;
+ Withholding Tax Calculation and Certifications;
+ Statutory and tax compliance activities;
+ Management and printing of Statutory Accounting Registers;
+ Carry out sophisticated accounting treatment and prepares financial documents and supplementary reporting
+ Ensure compliance with company policy, approval authority matrix and standard operating procedure; recommends changes to strengthen control environment
+ Drive continuous improvement and uses systems to increase controls and efficiencies
+ Perform local taxes calculations;
+ FOC Reports analysis and issue of the monthly Self invoices;
+ External Agents commission calculation and related communications (Sales Target, Enasarco and FIRR);
+ Control of the payment lists:
+ Draft calculation of year end corporate taxes;
+ Support to the External TAX Consultants for the Statutory Report and the Annual TAX Declarations;
+ Support to the external Auditor for quarter and year end data;
+ Administrative support to the Italian Subsidiary;
+ Other activities related to the role.
**Requirements:**
+ A bachelor's degree is preferred, along with 5-10 years of experience in accounting and tax.
+ Excellent understanding of financial accounting standards and internal controls.
+ Excellent user of Excel and PowerPoint
+ experience with IFS ERP (or equivalent) is a plus.
+ Proficient verbal and written communication skills (Italian and English).
**Travel requirements:**
+ Domestic/international travel required rarely
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, our Finance teams are important to our business and functional teams to make educated, sound decisions that drive our Mission and make us a stable and trusted industry leader. From Financial Planning & Analysis, Tax, Treasury, Financial Reporting, Audit, Investor Relations, Strategy & Corporate Development to Accounting, our Finance functions have a diverse and global presence, providing significant opportunities to develop outstanding career experiences and perspectives.
**How you will make an impact:**
The Italian Subsidiary of the Protein Diagnostics Division of Thermo Fisher, offers medical devices to all the Italian main Hospitals.
If you have a passion for financial accuracy and timeliness across a global, multi-faceted organization, Thermo Fisher Scientific's Accounting and Controllership function is the team for you. With a keen understanding of laws, regulations and compliance as well as reporting requirements consistent with ITA GAAP, this team uses innovative financial systems and controls, data security and robust processes to protect the company's assets and support its short- and long-term growth on a global scale. From technical accounting to budgeting and forecasting to planning and reporting, you will build relationships with internal and external audit teams as well as key business partners to drive sophisticated business decisions. You will have an opportunity to build strong organizational alliances to understand and mitigate risk, as well as capture opportunities and provide valuable support to all business partners.
Seeking a **proficient finance team member** who will provide finance, accounting and compliance to the Italian business. The successful candidate will implement accounting, controls and compliance procedures to ensure timely and accurate financial reporting. In addition, the position holder will identify and recommend operational improvement opportunities, and support leadership in achieving of business objectives.
**What you will do** :
+ Monthly and year end accounting vouchers, closing activities including journal entries, accruals, reporting and analysis;
+ Management of monthly VAT registers, VAT quarterly declaration data (LIPE), and VAT annual declaration data;
+ Fixed Assets monthly updates, depreciation and scrapping;
+ Analysis of customers collections for the bank update and the monthly collections report;
+ Balance Sheet Reconciliations;
+ Withholding Tax Calculation and Certifications;
+ Statutory and tax compliance activities;
+ Management and printing of Statutory Accounting Registers;
+ Carry out sophisticated accounting treatment and prepares financial documents and supplementary reporting
+ Ensure compliance with company policy, approval authority matrix and standard operating procedure; recommends changes to strengthen control environment
+ Drive continuous improvement and uses systems to increase controls and efficiencies
+ Perform local taxes calculations;
+ FOC Reports analysis and issue of the monthly Self invoices;
+ External Agents commission calculation and related communications (Sales Target, Enasarco and FIRR);
+ Control of the payment lists:
+ Draft calculation of year end corporate taxes;
+ Support to the External TAX Consultants for the Statutory Report and the Annual TAX Declarations;
+ Support to the external Auditor for quarter and year end data;
+ Administrative support to the Italian Subsidiary;
+ Other activities related to the role.
**Requirements:**
+ A bachelor's degree is preferred, along with 5-10 years of experience in accounting and tax.
+ Excellent understanding of financial accounting standards and internal controls.
+ Excellent user of Excel and PowerPoint
+ experience with IFS ERP (or equivalent) is a plus.
+ Proficient verbal and written communication skills (Italian and English).
**Travel requirements:**
+ Domestic/international travel required rarely
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
4
Production Quality Specialist
ThermoFisher Scientific
Oggi
Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join our high-performing team at Thermo Fisher Scientific, where you'll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier, cleaner, and safer. As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.
REQUIREMENTS:
- Bachelor's Degree required, no prior experience required, preferably in a GMP manufacturing environment
- Preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field
- Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous
- Thorough knowledge of FDA, EMA, and international GMP regulations
- Proven ability to review and approve GMP documentation, batch records, and quality records
- Strong understanding of quality management systems and tools (e.g. CAPA, change control)
- Excellent documentation and technical writing skills
- Proficiency with quality systems software and Microsoft Office applications
- Strong analytical and problem-solving abilities with keen attention to detail
- Outstanding verbal and written communication skills
- Ability to work independently and collaborate effectively across functions
- Experience conducting quality investigations and root cause analysis
- Knowledge of environmental monitoring and contamination control principles
- Flexibility to work various shifts as needed to support manufacturing operations
- Ability to gown and work in controlled manufacturing environments when required
- Physical capability to stand, walk, and lift up to 25 pounds occasionally
- Sound judgment and decision-making skills
- Commitment to maintaining a quality-focused culture and driving continuous improvement
- Fluency in English required; additional language skills beneficial
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join our high-performing team at Thermo Fisher Scientific, where you'll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier, cleaner, and safer. As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.
REQUIREMENTS:
- Bachelor's Degree required, no prior experience required, preferably in a GMP manufacturing environment
- Preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field
- Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous
- Thorough knowledge of FDA, EMA, and international GMP regulations
- Proven ability to review and approve GMP documentation, batch records, and quality records
- Strong understanding of quality management systems and tools (e.g. CAPA, change control)
- Excellent documentation and technical writing skills
- Proficiency with quality systems software and Microsoft Office applications
- Strong analytical and problem-solving abilities with keen attention to detail
- Outstanding verbal and written communication skills
- Ability to work independently and collaborate effectively across functions
- Experience conducting quality investigations and root cause analysis
- Knowledge of environmental monitoring and contamination control principles
- Flexibility to work various shifts as needed to support manufacturing operations
- Ability to gown and work in controlled manufacturing environments when required
- Physical capability to stand, walk, and lift up to 25 pounds occasionally
- Sound judgment and decision-making skills
- Commitment to maintaining a quality-focused culture and driving continuous improvement
- Fluency in English required; additional language skills beneficial
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
5
Senior Medical Writer (Publications)
Remota
ThermoFisher Scientific
Oggi
Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier, cleaner, and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Effective communication of evidence and information is essential to conveying the value of products. Our highly trained staff provide medical writing services for the peri- and post-approval phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standards, and corporate guidance.
**Discover Impactful Work**
The Publications and Scientific Communications team, part of the Medical Writing and Healthcare Communications department at Thermo Fisher Scientific, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**What You'll Do in the Role**
+ Write, edit, and manage **manuscripts, posters, abstracts, oral presentation slide decks, and review articles** , on time, within budget, and with little instruction
+ Raise and help resolve project management issues, such as out-of-scope requests
+ Ensure compliance with quality processes and industry standards
+ Represent the team as the lead contact on projects
+ Lead or provide input on process improvements
**Keys to Success**
We are looking for an expert publication writer to join the team. The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have extensive experience in creating publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek a bright teammate who is proactive, enjoys challenges, and can thrive in a highly collaborative CRO (contract research organization) environment.
**Education, Experience & Skills**
+ Extensive proven experience as a writer of peer-reviewed medical publications
+ Experience working in a CRO environment preferred
+ Experience of generating publication extenders (e.g., plain language summaries, video/graphical abstracts) advantageous
+ Experience of publication planning/strategy advantageous
+ Excellent scientific writing, project management, and digital literacy
+ Bachelor's degree or higher in a scientific field; advanced degree preferred
+ In-depth knowledge of different therapeutic areas
+ Additional qualifications (e.g., EMWA or CMPP certification) advantageous
+ Sound professional judgement in dealing with inquiries, issues, and customer concerns
+ Able to independently make decisions and solve problems
+ Comfortable working on multiple projects concurrently
+ Able to prioritize and delegate tasks effectively
+ Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
**Physical Requirements / Work Environment**
+ Work will be 100% remote (home based)
+ Occasional domestic and international travel may be required
**Why Join Us?**
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other legally protected status.
**NOTE: Please include in your application a cover letter describing your qualifications for the role.**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier, cleaner, and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Effective communication of evidence and information is essential to conveying the value of products. Our highly trained staff provide medical writing services for the peri- and post-approval phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standards, and corporate guidance.
**Discover Impactful Work**
The Publications and Scientific Communications team, part of the Medical Writing and Healthcare Communications department at Thermo Fisher Scientific, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**What You'll Do in the Role**
+ Write, edit, and manage **manuscripts, posters, abstracts, oral presentation slide decks, and review articles** , on time, within budget, and with little instruction
+ Raise and help resolve project management issues, such as out-of-scope requests
+ Ensure compliance with quality processes and industry standards
+ Represent the team as the lead contact on projects
+ Lead or provide input on process improvements
**Keys to Success**
We are looking for an expert publication writer to join the team. The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have extensive experience in creating publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek a bright teammate who is proactive, enjoys challenges, and can thrive in a highly collaborative CRO (contract research organization) environment.
**Education, Experience & Skills**
+ Extensive proven experience as a writer of peer-reviewed medical publications
+ Experience working in a CRO environment preferred
+ Experience of generating publication extenders (e.g., plain language summaries, video/graphical abstracts) advantageous
+ Experience of publication planning/strategy advantageous
+ Excellent scientific writing, project management, and digital literacy
+ Bachelor's degree or higher in a scientific field; advanced degree preferred
+ In-depth knowledge of different therapeutic areas
+ Additional qualifications (e.g., EMWA or CMPP certification) advantageous
+ Sound professional judgement in dealing with inquiries, issues, and customer concerns
+ Able to independently make decisions and solve problems
+ Comfortable working on multiple projects concurrently
+ Able to prioritize and delegate tasks effectively
+ Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
**Physical Requirements / Work Environment**
+ Work will be 100% remote (home based)
+ Occasional domestic and international travel may be required
**Why Join Us?**
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other legally protected status.
**NOTE: Please include in your application a cover letter describing your qualifications for the role.**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
6
(Law 68/99) PDS Administrative Assistant I
ThermoFisher Scientific
Oggi
Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join us as PDS Administrative Assistant I at Thermo Fisher Scientific, where you'll contribute to our mission of making the world healthier, cleaner, and safer. You'll provide essential administrative support across various functions while working with professionals who value excellence and innovation. You'll manage day-to-day operations including document handling, supply management, meeting coordination, and visitor support. Your attention to detail and organizational skills will help maintain smooth operations while supporting our team's success. This position offers opportunities to work with stakeholders while developing professional skills in a collaborative environment.
REQUIREMENTS:
- You are registered under Protected Categories, Art. 1 / 18 of Law 68/99
- No prior experience is required
- Professional certification preferred
- Additional relevant certifications a plus
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Strong organizational and time management skills
- Excellent written and verbal communication abilities
- Detail-oriented with high accuracy in administrative tasks
- Ability to handle confidential information professionally
- Experience with office equipment and procedures
- Strong multitasking capabilities
- Customer service-oriented mindset
- Ability to work both independently and collaboratively
- Professional demeanor
- Excellent interpersonal skills for working with diverse groups
- Ability to prioritize and manage multiple tasks simultaneously
- Basic knowledge of filing systems and records management
- Physical ability to perform office tasks including sitting for extended periods
- May require occasional travel based on business needs
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join us as PDS Administrative Assistant I at Thermo Fisher Scientific, where you'll contribute to our mission of making the world healthier, cleaner, and safer. You'll provide essential administrative support across various functions while working with professionals who value excellence and innovation. You'll manage day-to-day operations including document handling, supply management, meeting coordination, and visitor support. Your attention to detail and organizational skills will help maintain smooth operations while supporting our team's success. This position offers opportunities to work with stakeholders while developing professional skills in a collaborative environment.
REQUIREMENTS:
- You are registered under Protected Categories, Art. 1 / 18 of Law 68/99
- No prior experience is required
- Professional certification preferred
- Additional relevant certifications a plus
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Strong organizational and time management skills
- Excellent written and verbal communication abilities
- Detail-oriented with high accuracy in administrative tasks
- Ability to handle confidential information professionally
- Experience with office equipment and procedures
- Strong multitasking capabilities
- Customer service-oriented mindset
- Ability to work both independently and collaboratively
- Professional demeanor
- Excellent interpersonal skills for working with diverse groups
- Ability to prioritize and manage multiple tasks simultaneously
- Basic knowledge of filing systems and records management
- Physical ability to perform office tasks including sitting for extended periods
- May require occasional travel based on business needs
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
7
Team leader, PDS FD/AD Lab
ThermoFisher Scientific
Oggi
Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Laboratory Setting
**Job Description**
. As Laboratory Team Leader, you'll coordinate and oversee formulation and analytical activities while ensuring compliance with GMP standards and client expectations. This role combines technical expertise with leadership, as you'll guide a team of analysts while conducting sophisticated analytical work supporting product development, stability testing, and method validation.
You'll manage laboratory operations, from coordinating testing schedules to resolving complex analytical challenges. Working with advanced instrumentation, you'll ensure the highest quality standards in testing raw materials, in-process samples, and finished products. Your expertise will be essential in method development, validation, and transfer activities, while maintaining strong relationships with internal teams and external clients.
This position offers the opportunity to contribute to pharmaceutical development while growing your leadership skills and technical expertise in a collaborative, innovative environment.
REQUIREMENTS:
- Advanced Degree with no prior experience required, OR Bachelor's Degree plus 2 years of experience in pharmaceutical, biotechnology, or related industry
- Preferred Fields of Study: Chemistry, Chemical Engineering, Biology, Biotechnology, Pharmaceutical Sciences, or related field
- Expertise in analytical techniques and instrumentation (HPLC, GC, FT-IR, UV-Spectrophotometer)
- Demonstrated proficiency in method development, validation, and transfer
- Strong working knowledge of GMP regulations and pharmaceutical quality systems
- Experience with laboratory information management systems and Empower software
- Leadership and team management experience
- Project management and organizational skills
- Problem-solving and analytical troubleshooting capabilities
- Proficient in MS Office applications
- Written and verbal communication skills in English
- Ability to interact effectively with clients and cross-functional teams
- Experience in conducting laboratory investigations and OOS investigations
- Knowledge of data integrity principles (ALCOA)
- Ability to prepare and review technical documentation and reports
- Physical capabilities to perform laboratory work, including standing for extended periods
- Ability to adapt to changing priorities and deadlines
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Laboratory Setting
**Job Description**
. As Laboratory Team Leader, you'll coordinate and oversee formulation and analytical activities while ensuring compliance with GMP standards and client expectations. This role combines technical expertise with leadership, as you'll guide a team of analysts while conducting sophisticated analytical work supporting product development, stability testing, and method validation.
You'll manage laboratory operations, from coordinating testing schedules to resolving complex analytical challenges. Working with advanced instrumentation, you'll ensure the highest quality standards in testing raw materials, in-process samples, and finished products. Your expertise will be essential in method development, validation, and transfer activities, while maintaining strong relationships with internal teams and external clients.
This position offers the opportunity to contribute to pharmaceutical development while growing your leadership skills and technical expertise in a collaborative, innovative environment.
REQUIREMENTS:
- Advanced Degree with no prior experience required, OR Bachelor's Degree plus 2 years of experience in pharmaceutical, biotechnology, or related industry
- Preferred Fields of Study: Chemistry, Chemical Engineering, Biology, Biotechnology, Pharmaceutical Sciences, or related field
- Expertise in analytical techniques and instrumentation (HPLC, GC, FT-IR, UV-Spectrophotometer)
- Demonstrated proficiency in method development, validation, and transfer
- Strong working knowledge of GMP regulations and pharmaceutical quality systems
- Experience with laboratory information management systems and Empower software
- Leadership and team management experience
- Project management and organizational skills
- Problem-solving and analytical troubleshooting capabilities
- Proficient in MS Office applications
- Written and verbal communication skills in English
- Ability to interact effectively with clients and cross-functional teams
- Experience in conducting laboratory investigations and OOS investigations
- Knowledge of data integrity principles (ALCOA)
- Ability to prepare and review technical documentation and reports
- Physical capabilities to perform laboratory work, including standing for extended periods
- Ability to adapt to changing priorities and deadlines
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Candidati ora
8
Principal Medical Writer (Publications)
Remota
ThermoFisher Scientific
Oggi
Lavoro visualizzato
Descrizione Del Lavoro
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Effective communication of evidence and information is essential to conveying the value of products. With approximately 20 years of experience, our highly trained staff provide medical writing services for all phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standard processes, and your corporate guidance.
**IMPORTANT: a cover letter describing your qualifications is required, along with your resume to be considered.**
**Discover Impactful Work**
The Publications and Scientific Communications team, a part of Medical Writing and Healthcare Communications, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**A day in the life:**
· Write, edit, and handle publications and other scientific communications (manuscripts, posters, abstracts, oral presentation slide decks, and review articles), on time, within budget, and with little instruction. Provides senior review of documents.
· Appropriately resolve or raise project management issues, such as out-of-scope activities
· Ensure compliance with quality processes and requirements
· Represent the team as a prime contact on projects, establishes clients relationships.
· Assist in business development initiatives
· Lead or provide input on initiatives for process improvement, provides training and mentorship of other writers.
**Keys to Success:**
We are looking for an expert publications' writer to join the team. The Principal Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from conception to completion. The successful candidate will have extensive experience in writing publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek an excellent teammate who is proactive, enjoys challenges, can work on multiple projects concurrently, and is can work in a highly collaborative CRO environment.
**Education and Experience**
· Extensive proven experience as a writer of peer-reviewed medical publications (comparable to 8+ years); experience working in a CRO environment preferred
· Excellent scientific writing, project management, and digital literacy
· Bachelor's degree or higher in a scientific field; advanced degree preferred
· In-depth knowledge of relevant specialty areas of medicine
· Additional qualifications (AMWA, EMWA, or RAC training; CMPP certification) advantageous
· Excellent written English. Proactive communicator
· Sound professional judgement in dealing with inquiries, issues, and customer concerns; able to independently make decisions and solve problems
· Comfortable working on multiple projects concurrently
· Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Effective communication of evidence and information is essential to conveying the value of products. With approximately 20 years of experience, our highly trained staff provide medical writing services for all phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standard processes, and your corporate guidance.
**IMPORTANT: a cover letter describing your qualifications is required, along with your resume to be considered.**
**Discover Impactful Work**
The Publications and Scientific Communications team, a part of Medical Writing and Healthcare Communications, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**A day in the life:**
· Write, edit, and handle publications and other scientific communications (manuscripts, posters, abstracts, oral presentation slide decks, and review articles), on time, within budget, and with little instruction. Provides senior review of documents.
· Appropriately resolve or raise project management issues, such as out-of-scope activities
· Ensure compliance with quality processes and requirements
· Represent the team as a prime contact on projects, establishes clients relationships.
· Assist in business development initiatives
· Lead or provide input on initiatives for process improvement, provides training and mentorship of other writers.
**Keys to Success:**
We are looking for an expert publications' writer to join the team. The Principal Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from conception to completion. The successful candidate will have extensive experience in writing publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek an excellent teammate who is proactive, enjoys challenges, can work on multiple projects concurrently, and is can work in a highly collaborative CRO environment.
**Education and Experience**
· Extensive proven experience as a writer of peer-reviewed medical publications (comparable to 8+ years); experience working in a CRO environment preferred
· Excellent scientific writing, project management, and digital literacy
· Bachelor's degree or higher in a scientific field; advanced degree preferred
· In-depth knowledge of relevant specialty areas of medicine
· Additional qualifications (AMWA, EMWA, or RAC training; CMPP certification) advantageous
· Excellent written English. Proactive communicator
· Sound professional judgement in dealing with inquiries, issues, and customer concerns; able to independently make decisions and solve problems
· Comfortable working on multiple projects concurrently
· Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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