93 Posti di lavoro per Synlab in Italia

We are looking for individuals who want to join our Team in Germany, the UK, and Italy, Europe.

Apply Now!

• Title: Medical Laboratory Technician
• Location: US Army Europe
• Start Date: 1st October 2025
• Job Type: Full Time

Healthcare Professionals are needed to provide medical services to support the Military Treatment Facilities and Health Clinics within US Army Medical Command, Regional Health Command Europe, and other Department of Defense (DoD) agencies including US Navy and US Air Forces in Europe.

• Degree: Certificate from an accredited medical laboratory technician training program (NAACLS, ABHES, or acceptable to AMT).
• Certification: Certification/registration as determined by the American Society for Clinical Pathology (ASCP) or AMT.
• Experience: Knowledge of standard and molecular laboratory techniques or at least 2 years of work experience as a clinical laboratory technician in the last 5 years.

• Perform clinical laboratory tests in hematology, chemistry, cytology, histotechnology, urinalysis, serology, microbiology, and blood bank.
• Determine specimen suitability, prepare specimens, and maintain physiological properties.
• Prepare reagents, calibrate instruments, verify operation, and troubleshoot.
• Conduct quality control procedures, maintain records, and ensure proper specimen transport and disposal.
• Perform patient testing, including nucleic acid extraction, PCR, DNA sequencing, and microbiological methods.
• Report results accurately into the LIS (CHCS), maintain records for at least two years.
• Participate in Quality Control/Quality Management protocols, SOP review, and safety procedures.
• Handle reporting, result certification, and epidemiological surveillance tasks.
• Comply with training, safety, and external support requirements, including specimen tracking and additional duties as assigned.

This position is eligible for support under NATO Status of Forces Agreement (SOFA) articles 72 or 73.

For more information, visit our website. Upload your resume directly at our application portal.

French Consulting is proud to be an equal opportunity workplace and affirmative action employer. We are committed to diversity and inclusion in employment, considering all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.

J-18808-Ljbffr

We are looking for individuals who want to join our Team in Germany, the UK and Italy, Europe.

Apply Now!

JOBOPENING

• Title : Medical Laboratory Technician
• Location : US Army Europe
• Start Date : 1st October 2025
• Job-Type : Full Time

Job Overview Healthcare Professionals are needed to provide medical services to supplement the medical staff in support of the Military Treatment Facilities and Health Clinics within US Army Medical Command, Regional Health Command Europe and for other Department of Defense (DoD) agencies including US Navy and US Air Forces in Europe.

Qualifications

Degree : Certificate.

• Education : Graduate from a medical laboratory technician training program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or the Accrediting Bureau of Health Education Schools (ABHES) or educational program acceptable to the American Medical Technologist (AMT).
• Certification : Certification / registration as determined by the American Society for Clinical Pathology (ASCP) or AMT as specified in the TO.
• Experience : Knowledge of standard and molecular laboratory techniques and concepts in traditional and molecular Infectious Disease testing, (or) shows work experience as a clinical laboratory technician over at least 2 of the last 5 years.

Responsibilities Include but are not limited to :

Perform a full range of clinical laboratory tests in any one or a combination of the following sections of the laboratory : hematology, chemistry, cytology, histotechnology, urinalysis, serology, microbiology and blood bank as outlined in the TO.

• Determine the suitability of specimens for analysis. Prepare specimens for analysis and ensure that the physiologic state of the properties is maintained.
• Prepare reagents and primary reference materials as necessary. Calibrate, standardize, adjust, and maintain instruments. Verify correct instrument operation using established procedures and quality control checks. Identify the cause of common problems and make simple repairs.
• Recognize and react to indicators of malfunction. Locate and implement corrections. Obtain analytical data, convert to a prescribed unit of reporting, as necessary, and correlate data to verify results.
• Conduct quality control procedures on equipment, reagents and products and maintain proper records for quality control and quality assurance reports.
• Prepare specimens for transport to MTF laboratory or for mail out.
• Prepare biological waste for proper disposal.
• Patient testing duties : examples of these duties include specimen processing; nucleic acid extraction, amplification, detection (PCR based techniques); real-time PCR techniques; DNA sequencing; other tasks and techniques associated with microbiological, viral and molecular methods (to include detection of influenza viruses, gastrointestinal pathogens and toxins, hemorrhagic fever viruses, and other emerging respiratory viruses that adversely affect patient disposition).
• Patient Test reporting : Report results into the LIS (CHCS); ensure all work documents are accurate and completed in full; maintain all records for a minimum period of two years.
• Quality Control / Quality Management requirements : Comply and participate in all Quality Control / Quality Management protocols and procedures as applicable to the tasks identified in this PWS. This includes (but is not limited to) performing Quality Control procedures applicable to testing performed and equipment used; review and comply with established SOPs; comply with all training, on-going education and safety requirements;
• Reporting and administrative requirements : this includes but is not limited to participating in result certification; report generation; and SOP review and modification as required by supervisor or designee; maintain a weekly epidemiological report of surveillance testing results and submit results on a weekly basis to Public Health Command / GEIS representatives; assist in researching procedures, manuscripts and documents related to disease surveillance.
• Training and Safety : complies with all technical, MTF and unit specific training requirements.
• External Training and Tracking Requirements : Participate in training to outlying clinics (as required); track related expenditures to project renewable costs; review weekly trends in resulting for submission to preventive medicine and host nation officials as needed; maintain and submit specimen surveys as required.
• Specimen Tracking : Recruit submission of specimens from outlying clinics on a weekly basis; ensure that specimen surveys are filled out and included with specimens; ensure that testing results are regularly submitted and received by participating clinics.
• Perform additional tasks as assigned within the scope of a regular laboratory technician, Quality Control / Quality Management and disease surveillance duties.

DOCPER / SOFA / Logistical Support Status

This position is eligible for support under NATO Status of Forces Agreement (SOFA) supplemental agreement articles 72 or 73.

APPLICATION PROCESS

For more information, go to our website. Upload your resume directly at

French Consulting is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

J-18808-Ljbffr

We are looking for individuals who want to join our Team in Germany, the UK and Italy, Europe.

Apply Now!

JOBOPENING

• Title : Medical Laboratory Technician
• Location : US Army Europe
• Start Date : 1st October 2025
• Job-Type : Full Time

Job Overview Healthcare Professionals are needed to provide medical services to supplement the medical staff in support of the Military Treatment Facilities and Health Clinics within US Army Medical Command, Regional Health Command Europe and for other Department of Defense (DoD) agencies including US Navy and US Air Forces in Europe.

Qualifications

Degree : Certificate.

• Education : Graduate from a medical laboratory technician training program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or the Accrediting Bureau of Health Education Schools (ABHES) or educational program acceptable to the American Medical Technologist (AMT).
• Certification : Certification / registration as determined by the American Society for Clinical Pathology (ASCP) or AMT as specified in the TO.
• Experience : Knowledge of standard and molecular laboratory techniques and concepts in traditional and molecular Infectious Disease testing, (or) shows work experience as a clinical laboratory technician over at least 2 of the last 5 years.

Responsibilities Include but are not limited to :

Perform a full range of clinical laboratory tests in any one or a combination of the following sections of the laboratory : hematology, chemistry, cytology, histotechnology, urinalysis, serology, microbiology and blood bank as outlined in the TO.

• Determine the suitability of specimens for analysis. Prepare specimens for analysis and ensure that the physiologic state of the properties is maintained.
• Prepare reagents and primary reference materials as necessary. Calibrate, standardize, adjust, and maintain instruments. Verify correct instrument operation using established procedures and quality control checks. Identify the cause of common problems and make simple repairs.
• Recognize and react to indicators of malfunction. Locate and implement corrections. Obtain analytical data, convert to a prescribed unit of reporting, as necessary, and correlate data to verify results.
• Conduct quality control procedures on equipment, reagents and products and maintain proper records for quality control and quality assurance reports.
• Prepare specimens for transport to MTF laboratory or for mail out.
• Prepare biological waste for proper disposal.
• Patient testing duties : examples of these duties include specimen processing; nucleic acid extraction, amplification, detection (PCR based techniques); real-time PCR techniques; DNA sequencing; other tasks and techniques associated with microbiological, viral and molecular methods (to include detection of influenza viruses, gastrointestinal pathogens and toxins, hemorrhagic fever viruses, and other emerging respiratory viruses that adversely affect patient disposition).
• Patient Test reporting : Report results into the LIS (CHCS); ensure all work documents are accurate and completed in full; maintain all records for a minimum period of two years.
• Quality Control / Quality Management requirements : Comply and participate in all Quality Control / Quality Management protocols and procedures as applicable to the tasks identified in this PWS. This includes (but is not limited to) performing Quality Control procedures applicable to testing performed and equipment used; review and comply with established SOPs; comply with all training, on-going education and safety requirements;
• Reporting and administrative requirements : this includes but is not limited to participating in result certification; report generation; and SOP review and modification as required by supervisor or designee; maintain a weekly epidemiological report of surveillance testing results and submit results on a weekly basis to Public Health Command / GEIS representatives; assist in researching procedures, manuscripts and documents related to disease surveillance.
• Training and Safety : complies with all technical, MTF and unit specific training requirements.
• External Training and Tracking Requirements : Participate in training to outlying clinics (as required); track related expenditures to project renewable costs; review weekly trends in resulting for submission to preventive medicine and host nation officials as needed; maintain and submit specimen surveys as required.
• Specimen Tracking : Recruit submission of specimens from outlying clinics on a weekly basis; ensure that specimen surveys are filled out and included with specimens; ensure that testing results are regularly submitted and received by participating clinics.
• Perform additional tasks as assigned within the scope of a regular laboratory technician, Quality Control / Quality Management and disease surveillance duties.

DOCPER / SOFA / Logistical Support Status

This position is eligible for support under NATO Status of Forces Agreement (SOFA) supplemental agreement articles 72 or 73.

APPLICATION PROCESS

For more information, go to our website. Upload your resume directly at

French Consulting is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

J-18808-Ljbffr

We are looking for individuals who want to join our Team in Germany, the UK and Italy, Europe.

Apply Now!

JOBOPENING

• Title : Medical Laboratory Technician
• Location : US Army Europe
• Start Date : 1st October 2025
• Job-Type : Full Time

Job Overview Healthcare Professionals are needed to provide medical services to supplement the medical staff in support of the Military Treatment Facilities and Health Clinics within US Army Medical Command, Regional Health Command Europe and for other Department of Defense (DoD) agencies including US Navy and US Air Forces in Europe.

Qualifications

Degree : Certificate.

• Education : Graduate from a medical laboratory technician training program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or the Accrediting Bureau of Health Education Schools (ABHES) or educational program acceptable to the American Medical Technologist (AMT).
• Certification : Certification / registration as determined by the American Society for Clinical Pathology (ASCP) or AMT as specified in the TO.
• Experience : Knowledge of standard and molecular laboratory techniques and concepts in traditional and molecular Infectious Disease testing, (or) shows work experience as a clinical laboratory technician over at least 2 of the last 5 years.

Responsibilities Include but are not limited to :

Perform a full range of clinical laboratory tests in any one or a combination of the following sections of the laboratory : hematology, chemistry, cytology, histotechnology, urinalysis, serology, microbiology and blood bank as outlined in the TO.

• Determine the suitability of specimens for analysis. Prepare specimens for analysis and ensure that the physiologic state of the properties is maintained.
• Prepare reagents and primary reference materials as necessary. Calibrate, standardize, adjust, and maintain instruments. Verify correct instrument operation using established procedures and quality control checks. Identify the cause of common problems and make simple repairs.
• Recognize and react to indicators of malfunction. Locate and implement corrections. Obtain analytical data, convert to a prescribed unit of reporting, as necessary, and correlate data to verify results.
• Conduct quality control procedures on equipment, reagents and products and maintain proper records for quality control and quality assurance reports.
• Prepare specimens for transport to MTF laboratory or for mail out.
• Prepare biological waste for proper disposal.
• Patient testing duties : examples of these duties include specimen processing; nucleic acid extraction, amplification, detection (PCR based techniques); real-time PCR techniques; DNA sequencing; other tasks and techniques associated with microbiological, viral and molecular methods (to include detection of influenza viruses, gastrointestinal pathogens and toxins, hemorrhagic fever viruses, and other emerging respiratory viruses that adversely affect patient disposition).
• Patient Test reporting : Report results into the LIS (CHCS); ensure all work documents are accurate and completed in full; maintain all records for a minimum period of two years.
• Quality Control / Quality Management requirements : Comply and participate in all Quality Control / Quality Management protocols and procedures as applicable to the tasks identified in this PWS. This includes (but is not limited to) performing Quality Control procedures applicable to testing performed and equipment used; review and comply with established SOPs; comply with all training, on-going education and safety requirements;
• Reporting and administrative requirements : this includes but is not limited to participating in result certification; report generation; and SOP review and modification as required by supervisor or designee; maintain a weekly epidemiological report of surveillance testing results and submit results on a weekly basis to Public Health Command / GEIS representatives; assist in researching procedures, manuscripts and documents related to disease surveillance.
• Training and Safety : complies with all technical, MTF and unit specific training requirements.
• External Training and Tracking Requirements : Participate in training to outlying clinics (as required); track related expenditures to project renewable costs; review weekly trends in resulting for submission to preventive medicine and host nation officials as needed; maintain and submit specimen surveys as required.
• Specimen Tracking : Recruit submission of specimens from outlying clinics on a weekly basis; ensure that specimen surveys are filled out and included with specimens; ensure that testing results are regularly submitted and received by participating clinics.
• Perform additional tasks as assigned within the scope of a regular laboratory technician, Quality Control / Quality Management and disease surveillance duties.

DOCPER / SOFA / Logistical Support Status

This position is eligible for support under NATO Status of Forces Agreement (SOFA) supplemental agreement articles 72 or 73.

APPLICATION PROCESS

For more information, go to our website. Upload your resume directly at

French Consulting is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

J-18808-Ljbffr

Are you passionate about the intersection of finance, strategy, and healthcare innovation? Join a growing Transaction Services team in Milan , where you'll play a pivotal role in shaping the future of the Healthcare and Life Sciences (HCLS) sector.

You will support leading healthcare providers, biotech firms, pharma companies, and investors through high-stakes transactions, from due diligence to post-deal integration. My client is seeking a Manager-level professional who can lead complex projects, drive insights, and deliver value to clients in this dynamic and rapidly evolving space.

What you'll do :

• Lead financial due diligence engagements for M&A transactions in the HCLS sector
• Analyze key financial and operational data to assess business performance and identify value drivers and risks
• Manage client relationships and deliver high-impact reports and presentations
• Collaborate across cross-functional teams including strategy, valuation, and tax specialists
• Support business development and proposal efforts for new opportunities in the sector

I'm looking for :

• 5+ years of experience in Transaction Services, Deal Advisory, or Financial Due Diligence
• Strong knowledge of the healthcare and life sciences industry (pharma, medtech, providers, etc.)
• Excellent financial modeling, analytical, and communication skills
• Fluency in Italian and English
• A collaborative, entrepreneurial mindset with a focus on client service

Why jJoin this team?

• Work with top-tier clients and cutting-edge healthcare innovators
• Be part of a fast-paced, purpose-driven team in Milan's financial hub
• Continuous learning, professional development, and career growth opportunities
• Competitive compensation and flexible work culture

Are you passionate about the intersection of finance, strategy, and healthcare innovation? Join a growing Transaction Services team in Milan , where you'll play a pivotal role in shaping the future of the Healthcare and Life Sciences (HCLS) sector.

You will support leading healthcare providers, biotech firms, pharma companies, and investors through high-stakes transactions, from due diligence to post-deal integration. My client is seeking a Manager-level professional who can lead complex projects, drive insights, and deliver value to clients in this dynamic and rapidly evolving space.

What you'll do :

• Lead financial due diligence engagements for M&A transactions in the HCLS sector
• Analyze key financial and operational data to assess business performance and identify value drivers and risks
• Manage client relationships and deliver high-impact reports and presentations
• Collaborate across cross-functional teams including strategy, valuation, and tax specialists
• Support business development and proposal efforts for new opportunities in the sector

I'm looking for :

• 5+ years of experience in Transaction Services, Deal Advisory, or Financial Due Diligence
• Strong knowledge of the healthcare and life sciences industry (pharma, medtech, providers, etc.)
• Excellent financial modeling, analytical, and communication skills
• Fluency in Italian and English
• A collaborative, entrepreneurial mindset with a focus on client service

Why jJoin this team?

• Work with top-tier clients and cutting-edge healthcare innovators
• Be part of a fast-paced, purpose-driven team in Milan's financial hub
• Continuous learning, professional development, and career growth opportunities
• Competitive compensation and flexible work culture

Social network you want to login/join with:

Founded in 2003, InvenSense Inc., a TDK Group Company, is the world’s leading provider of MEMS sensor platforms. InvenSense’s vision of Sensing Everything targets the consumer electronics and industrial markets with integrated Motion and Sound solutions. Our solutions combine MEMS (micro electrical mechanical systems) sensors, such as accelerometers, gyroscopes, compasses, and microphones with proprietary algorithms and firmware that intelligently process, synthesize, and calibrate the output of sensors, maximizing performance and accuracy. InvenSense’s motion tracking, audio and location platforms, and services can be found in many of the world’s largest and most iconic brands including smartphones, tablets, wearables, drones, gaming devices, internet of things, automotive products, and remote controls for smart TVs.

InvenSense is headquartered in San Jose, CA and has offices in Boston, China, Taiwan, Korea, Japan, France, Canada, Slovakia, and Italy. We’re looking for top-notch Engineers to join our global team. If you’re interested in being part of our journey and helping us grow to become the leading provider of SoC platform solutions, we want to hear from you.

Job Description

1. Set up test apparatus and conduct product testing following test methods, procedures, and standards.
2. Support data post-processing and their organization on internal network.
3. Conduct product characterization and generate reports.
4. Install software and perform basic maintenance of test apparatus.
5. Communicate well with members of engineering department and other colleagues.

Qualifications

1. Basic technical knowledge of electrical and electronic principles.
2. Knowledge and experience in use of laboratory equipment such as oscilloscopes, temperature chambers, meters, and other electrical and electro-mechanical test equipment.
3. Comfortable with use of computer: mastering of MS Excel would be a plus. Basic knowledge of programming languages like C++, Python or others.
4. Familiarity with electronic board assembly and debugging is a plus.

At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation.

You Are :

We are seeking a Test & Validation Technician who is passionate about technology and innovation. You will be part of a dynamic R&D team dedicated to developing high-speed SerDes PHYs. The ideal candidate is someone with hands-on experience in a lab environment, who possesses a strong technical background and an eye for detail. You are someone who thrives in fast-paced settings, can manage multiple tasks simultaneously, and has excellent organizational skills. Your ability to communicate effectively, both verbally and in writing, is crucial. You are familiar with using PCB soldering tools and have a college diploma in electronics. Additionally, you have the capability to proficiently use Microsoft Office software tools. Experience with lab equipment and software programming (Matlab or Python) is a plus. Your proactive approach and problem-solving skills will be vital in ensuring the success of our projects.

What You’ll Be Doing :

• Performing PCB soldering and reworks
• Maintaining lab equipment in a safe, clean, orderly, and operational manner
• Assembling equipment according to detailed plans
• Ensuring equipment calibration is up-to-date
• Coordinating shipping, purchasing, and receiving of equipment / lab supplies
• Using diagnostic equipment to test high-speed analog integrated circuits on various platforms

The Impact You Will Have :

What You’ll Need :

Who You Are :

The Team You’ll Be A Part Of :

You will be joining a dedicated R&D team focused on developing high-speed SerDes PHYs. Our team thrives on collaboration and innovation, working together to push the boundaries of technology. We are committed to maintaining a supportive and dynamic work environment where every team member can contribute to their fullest potential.

Rewards and Benefits :

We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non-monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process.

J-18808-Ljbffr

J-18808-Ljbffr

We Are :

At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation.

You Are :

We are seeking a Test & Validation Technician who is passionate about technology and innovation. You will be part of a dynamic R&D team dedicated to developing high-speed SerDes PHYs. The ideal candidate is someone with hands-on experience in a lab environment, who possesses a strong technical background and an eye for detail. You are someone who thrives in fast-paced settings, can manage multiple tasks simultaneously, and has excellent organizational skills. Your ability to communicate effectively, both verbally and in writing, is crucial. You are familiar with using PCB soldering tools and have a college diploma in electronics. Additionally, you have the capability to proficiently use Microsoft Office software tools. Experience with lab equipment and software programming (Matlab or Python) is a plus. Your proactive approach and problem-solving skills will be vital in ensuring the success of our projects.

What You’ll Be Doing :

• Performing PCB soldering and reworks
• Maintaining lab equipment in a safe, clean, orderly, and operational manner
• Assembling equipment according to detailed plans
• Ensuring equipment calibration is up-to-date
• Coordinating shipping, purchasing, and receiving of equipment / lab supplies
• Using diagnostic equipment to test high-speed analog integrated circuits on various platforms

The Impact You Will Have :

What You’ll Need :

Who You Are :

The Team You’ll Be A Part Of :

You will be joining a dedicated R&D team focused on developing high-speed SerDes PHYs. Our team thrives on collaboration and innovation, working together to push the boundaries of technology. We are committed to maintaining a supportive and dynamic work environment where every team member can contribute to their fullest potential.

Rewards and Benefits :

We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non-monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process.

J-18808-Ljbffr