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<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>Laboratory Analyst I - HiRes Prep (Multiple Shifts)</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><p>Eurofins Environment Testing is seeking a Laboratory Analyst to join our team! The Analyst I prepares and analyzes environmental samples using standard analytical techniques according to approved scientific methodology in compliance with Eurofins Environment Testing Quality Assurance programs and standard operating procedures (SOPs). This position can be physical job that may require standing for long periods, working with organic solvents, laboratory glassware and specialized equipment.</p><h4><strong>Essential Duties and Responsibilities:</strong></h4><ul><li>Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:<ul><li>Preparation of samples using standard techniques</li><li>Performing chemical analysis using standard techniques</li><li>Evaluation and quantification of data</li><li>Recording and reporting data and any unusual test occurrences to the supervisor</li><li>Performing routine instrument maintenance</li></ul></li><li>Competency on complex instrumentation instrument specific software (training is provided)</li><li>Responsible for keeping personal training documentation (training records, IDOC/DOC) current and accurate</li><li>Responsible for timely completion of assigned/scheduled QC samples (MDL, LOD/LOQ, PT)</li><li>As required, documents NCMs for projects with quality issues</li><li>Understands and utilizes backlog reports to manage personal workload.</li><li>Works under close supervision using routine and standard methods</li><li>Regular attendance and punctuality</li><li>Responsible for general housekeeping in work area</li><li>Proficient, with IDOCs, for a minimum for 50% of methods carried out in the department</li><li>Responsible for performing job functions in compliance with Eurofins Environment Testing environmental, health and safety and quality assurance standards</li><li>Demonstrates and promotes the company vision</li><li>Other duties as assigned</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>Minimum Education and Experience:</strong></h5><ul><li>BS or BA in chemistry or related field. 3 years laboratory experience may substitute for degree.</li><li>EPA method 1613, 1668 and 8290 experience would be beneficial</li><li>Laboratory experience helpful</li><li>Previous production-oriented work helpful (awareness and ability to meet deadlines)</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li><li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li></ul><h5><strong>Minimum Skills and Abilities:</strong></h5><ul><li>Perform calculations with mathematical formulas</li><li>Complete work within time and quality constraints</li><li>Demonstrate excellent time management and organizational skills</li><li>Demonstrate good problem solving skills</li><li>Work independently following written or verbal instructions</li><li>Cooperate and coordinate both orally and in writing</li><li>Participation in teamwork and meetings</li><li>Reading, writing and verbal skills</li></ul><h4><strong>Additional Preferences</strong></h4><ul><li>Ability to follow and learn appropriate protocols in at least one of the following disciplines:<ul><li>Organic preparation</li><li>SVOC analysis</li><li>Metals preparation and analysis</li><li>VOA preparation and analysis</li><li>General chemistry preparation and analysis</li></ul></li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>Position is full-time, non-exempt from overtime pay with flexibility for overtime and weekend coverage as needed. The candidate must be able to work one of the following shifts:</p><ul><li>Tuesday - Saturday, 12pm - 8:30pm</li><li>Monday - Friday, 3:30am - 12pm</li></ul><p><strong>The compensation for this position is $20.00 - $22.00 per hour commensurate with experience.</strong></p><p>Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location.</p><p>We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.</p><p>As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.</p><p><strong>We support your development!&nbsp;</strong>Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><strong>We embrace diversity!&nbsp;</strong>Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p><strong>Sustainability matters to us!</strong>&nbsp;At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler.</p><p>Find out more in our career page: <a target="_blank" rel="noopener noreferrer" href="https://careers.eurofins.com/">https://careers.eurofins.com/</a></p><h4><strong>Company description</strong>:&nbsp;</h4><p>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</p><p>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</p><p>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</p><p>In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.</p><p><strong>Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

Laboratory Analyst I - HiRes Prep (Multiple Shifts)

<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>Laboratory Technician I - SVOA Prep&nbsp;</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><p>Eurofins Environment Testing is seeking a Laboratory Technician to join our team! The Laboratory Technician, using general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins’ Quality Assurance programs and SOP’s, supports laboratory operations through general maintenance of laboratory and supply storage areas, equipment, instruments, and supplies.</p><h4><strong>Essential Duties and Responsibilities</strong></h4><p>Retrieves samples from Sample Control for analysis and maintains chain of custody.</p><h5><strong>Performs sample preparation which may include, but is not limited to, a combination of the following methods:</strong></h5><ul><li>Aliquot samples</li><li>Spike and trace samples</li><li>Prepare reagents/acids/bases</li><li>Bottle samples</li><li>Prepare concentrations</li><li>Separation</li><li>Sonication</li><li>Liquid rack set up</li></ul><p>Resolves discrepancies and anomalies to ensure samples are properly labeled.</p><p>Prepares general laboratory paperwork such as recording analysis results, tracking samples, bench sheets, and laboratory logbooks.</p><p>Washes laboratory glassware to prepare for next day’s samples.</p><p>Responsible for performing job functions within Eurofins Environment Testing America’s Environmental Health &amp; Safety and Quality Assurance standards.</p><p>Maintains housekeeping for work area.</p><p>Preforms daily calibration of pipettes and balances.</p><p>Properly disposes of hazardous and non-hazardous waste and recycling.</p><h4><strong>Secondary Duties</strong></h4><ul><li>Stocks laboratory supplies.</li><li>Cleans work area(s) to maintain a safe working environment.</li><li>Assists other laboratory areas as needed</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>Minimum Qualifications</strong></h5><ul><li>High school diploma or equivalent</li><li>High school Chemistry coursework, basic laboratory experience</li><li>Previous production-oriented work helpful (awareness and ability to meet deadlines)</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li><li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li></ul><h4><strong>Minimum Skills and Abilities</strong>:</h4><h5><strong>Skills</strong></h5><ul><li>Good Organization</li><li>Good Communication</li><li>Good Problem Solving</li></ul><h5><strong>Abilities</strong></h5><ul><li>Ability to Multi-task</li><li>Learn Quickly</li><li>Work Independently</li><li>Work within Time Constraints</li></ul><h5><strong>Knowledge</strong></h5><ul><li>General Knowledge of Chemistry and/or Science</li><li>Basic Mathematics</li><li>Knowledge of Production Work</li></ul><h5><strong>Requirements</strong></h5><ul><li>Working with Computers</li><li>Working with Laboratory Glassware</li><li>Working with Laboratory Instruments / Equipment</li><li>Use of Personal Protective Equipment</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>Position is full-time, non-exempt from overtime pay with flexibility for overtime and weekend coverage as needed. The candidate must be able to work&nbsp;<strong>Monday - Friday, 12:00pm - 8:30pm</strong></p><p><strong>The compensation for this position is $19.00 - $21.00 per hour commensurate with experience.</strong></p><p>Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant <strong>experience and skill set, base compensation of internal peers, business sector, and geographic location.</strong></p><h4><strong>What we Offer:</strong></h4><ul><li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li><li>Life and disability insurance</li><li>401(k) with company match</li><li>Paid vacation and holidays</li></ul><p><strong>We support your development! </strong>Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><strong>We embrace diversity!</strong> Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p><strong>Sustainability matters to us!</strong>&nbsp;At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler.</p><p><strong>Find out more in our career page: </strong><a target="_blank" rel="noopener noreferrer" href="https://careers.eurofins.com/ "><strong>https://careers.eurofins.com/&nbsp;</strong></a></p><p>Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and&nbsp;agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</p><p>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</p><p>In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.</p><p><strong>Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

Laboratory Technician I - SVOA Prep 

<p><strong>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.</strong></p><p>The Technology and User Services (TUS) group in NX is driven to help users use tools effectively to improve productivity and foster innovation. We deliver the Technology and User Services (TUS) group in NX to help customers use tools effectively to improve productivity and foster innovation. Our organization is here providing the technology backbone and devices that enable users to work in an office, lab or mobile environment.</p><h3><strong>TRD QA Specialist</strong></h3><p>During the pilot plant ramp up and operationalization support line units efforts in developing compliant manufacturing and QC-related quality system, with particular focus on master batch records, logbooks, forms, procedures. Oversee the manufacturing lines initial validation activities (e.g. water runs, engineering batches and eventually APSs) and QC laboratory instruments PQs.<br><br>In routine will be responsible to coordinate the QA shopfloor team and perform manufacturing and QC oversight, deviation and OOX review/approval, batch record review and support QP for the release of phase I/II clinical products.</p><h4><strong>Major Accountabilities:</strong></h4><ul><li>Support the pilot plant ramp‑up and operationalization by contributing to the development, implementation, and maintenance of a compliant manufacturing and QC quality system, with particular focus on master batch records, logbooks, forms, and GMP procedures.</li><li>Oversee and support initial manufacturing and QC validation activities, including water runs, engineering batches, APSs, and QC laboratory instrument Performance Qualifications (PQs), ensuring documentation completeness and GMP compliance.</li><li>In routine operations, coordinate and provide leadership to the QA shopfloor team, ensuring continuous QA presence during manufacturing and QC activities.</li><li>Perform real‑time manufacturing and QC oversight, including review and approval of deviations, OOX/OOS events, and execution of immediate quality decisions on the shopfloor.</li><li>Review, approve, and ensure completeness and accuracy of batch manufacturing records, supporting the Qualified Person (QP) in the timely release of Phase I/II clinical trial radiopharmaceutical products.</li><li>Ensure timely collection, monitoring, and reporting of Quality KPIs, supporting management reporting and continuous performance monitoring of manufacturing and QC activities.</li><li>Actively support Health Authority inspections and internal audits, ensuring timely provision of accurate documentation, data, and subject‑matter expertise, and contributing to inspection readiness activities.</li><li>Manage and oversee GxP Quality System processes, including Change Control, Deviation Management and CAPA, ensuring full compliance with GxP requirements and the Novartis Quality Manual.</li><li>Ensure effective tracking, escalation, and timely closure of CAPAs, including proactive management of risks related to delayed or ineffective actions.</li><li>Prepare, review, approve, and manage GxP documentation lifecycle activities, including document issuance, filing, archiving, and controlled distribution.</li><li>Actively contribute to continuous improvement initiatives, including optimization of existing processes and implementation of enhanced quality practices aligned with operational maturity of the pilot plant.</li></ul><h4><strong>Key Performance Indicators:</strong></h4><ul><li>Successful support of projects and routine operations in line with agreed quality standards and delivery timelines.</li><li>Positive outcomes of internal and external inspections, with no critical compliance gaps attributable to QA oversight.</li><li>Demonstrated ability to maintain effective collaboration and sound working relationships with manufacturing, QC, technical operations, and QA teams.</li><li>Consistent role modeling of Novartis culture, values, and behaviors within the QA organization and cross‑functional teams.</li></ul><h4><strong>Work Experience:</strong></h4><ul><li>Quality Assurance in pharmaceutical sterile manufacturing environments</li><li>Audit and Health Authority Inspection Management</li><li>Quality Management Systems (QMS)</li><li>Sterile Manufacturing Operations (DP or API)</li><li>Aseptic Processing and Contamination Control</li><li>Deviation, Incident, and Escalation Management</li><li>OOX/OOS and Investigation Management</li><li>Corrective and Preventive Actions (CAPA)</li><li>Change Control Management</li><li>SOP and Documentation Management</li><li>Manufacturing and QC Oversight</li></ul><h4><strong>Prerequisites:</strong></h4><ul><li>Proven experience of minimum 3 years working on the shopfloor of a sterile pharmaceutical manufacturing site (Drug Product or API).</li><li>Solid and demonstrable knowledge of Quality Systems, Data Integrity principles, and aseptic processing.</li><li>Experience working with electronic quality systems (e.g. change controls, deviations, OOX, complaints, etc.)</li><li>Strong quality mindset, leadership and cross‑functional attitude</li><li>Proactive and continuous improvement mindset</li></ul><h4><strong>Languages:</strong></h4><ul><li>Italian</li><li>English (intermediate level)</li></ul><p>Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</p>

TRD QA Specialist

<p><strong>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.</strong></p><p>The Technology and User Services (TUS) group in NX is driven to help users use tools effectively to improve productivity and foster innovation. We deliver the Technology and User Services (TUS) group in NX to help customers use tools effectively to improve productivity and foster innovation. Our organization is here providing the technology backbone and devices that enable users to work in an office, lab or mobile environment.</p><h3><strong>Site Quality Head (m/w/d)</strong></h3><p>In this role you will provide quality assurance oversight and be accountable for supporting Quality operations and provide technical and strategic leadership for all quality-related matters. Accountable to ensure compliance to GxP standards including product manufacturing and testing. You will also ensure Compliance with cGMP requirements and with the Novartis Quality Manual and policies.</p><h4><strong>Major Accountabilities:</strong></h4><ul><li>Provide leadership for strategic site initiatives, and represent site SLT quality in local cross-functional and global projects teams as team member or team leader that represent site quality.</li><li>Ensure all facilities, utilities and equipment are designed and installed to be operated in a safe and effective manner and are compliant with applicable standards</li><li>Ensure that during project phase planning, construction, commissioning, qualification (IQ, OQ and PQ) including any other validation activity complies with cGMP.</li><li>Timely escalation of risks in meeting timelines and / or budget incorporating site master planning and the long-term strategic plan.</li><li>Ensure adequate management of product critical quality issues (deviations, out of specifications). Ensure investigations are correctly executed and adequate CAPAs are defined, and proper follow up of CAPAs effectiveness. Review, provide guidance for, escalate where appropriate, and approve HA notifications (compliance related such as Exception requests, other).</li><li>Define, implement, monitor, consolidate and analyse Site Quality KPIs. Ensure Site Quality Committee is established, ensure relevant corrective and preventive actions are endorsed and implemented.</li><li>Drive for Site management team accountability. Coordinate the generation and monitor the execution of the Site Quality Plans, DI Plan, Site Quality Risk Assessments and other relevant gap assessments.</li><li>Hiring people, team building, people development and talent retention.</li></ul><h4><strong>Obligatory Requirements:</strong></h4><ul><li>Education: BS/MSc in Life Sciences and/or related experience.</li><li>10+ years of experience in GMP Pharmaceutical Manufacturing (including laboratory operations and Aseptic experience), at least 3 years combined of relevant experience in Quality Control and/or Quality Assurance covering quality areas.</li><li>Proven track record and practical experience in supporting a Quality Control operations unit and operating in full compliance with global cGMP requirements.</li><li>In-depth knowledge of cGMP regulations. Successfully managed inspections from major Health Authorities</li><li>Proven ability to manage multiple projects with moderate resource requirements, risk and/or complexity.</li><li>Fluent German and English, written and spoken.</li></ul>

Site Quality Head (m/w/d)

<p><strong>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.</strong></p><p>The Technology and User Services (TUS) group in NX is driven to help users use tools effectively to improve productivity and foster innovation. We deliver the Technology and User Services (TUS) group in NX to help customers use tools effectively to improve productivity and foster innovation. Our organization is here providing the technology backbone and devices that enable users to work in an office, lab or mobile environment.</p><h3><strong>Global Quality Control/Analytical Science and Technology Head</strong></h3><p>The Global Head RLT QC / AS&amp;T plays a crucial role in ensuring the quality and consistency of our products throughout their lifecycle. This role encompasses a wide range of responsibilities for the execution of strategy and the integration of all strategic and operational initiatives to ensure consistent and aligned standards across all laboratories, laboratory performance ("lean labs") and compliant analytical systems with competent and effective AS&amp;T and QC organizations in the RLT Platform. Acting in accordance with legislation, internal regulations, good practices and business goals. It is a key leadership position as part of the RLT Quality leadership team working closely with Site QC heads as well as other platform QC / AS&amp;T communities.</p><h4><strong>Major Accountabilities:</strong></h4><ul><li>Leading the implementation of a QC strategy, including method lifecycle strategy, global laboratory digital strategy, new method strategy, to increase the compliance and efficiency of QC laboratories in the RLT organization.</li><li>Enforcing global standardization/integration of business processes and information, data, global equipment standards and application architecture.</li><li>Enforcing the QC/AS&amp;T action plan by defining and implementing appropriate roadmaps for QC/AS&amp;T teams across the platform, ensuring compliance, continuous improvement and increasing the effectiveness of all types of QC testing. Initiating, implementing and sustaining initiatives defined by global QC/AS&amp;T.</li><li>Ensuring and promoting cross-site collaboration and transparency of joint initiatives, problems and lessons learned.</li><li>​ Supporting the development of on-site platform/team members in technical and leadership skills. Coaching and people development. Delivering training programs developed by the global QC/AS&amp;T function and actively participating in the development of relevant learning materials.</li><li>Proactively provide strong QA leadership to the business by ensuring considerable quality and organization awareness</li><li>Ensure adherence to global and local safety and regulatory internal and health authority standards.</li></ul><h4><strong>Requirements:</strong></h4><ul><li>Minimum degree in Pharmacy, Chemistry, Biology or related subject; higher level degree: MS, preferred but not required. Additional knowledge in Quality Assurance / Compliance</li><li>10+ years’ experience in GMP-regulated industries incl. QA/QC in Biotech area.</li><li>Solid working knowledge of FDA/EMA/ICH regulatory requirements</li><li>Broad cGMP experience with knowledge and understanding of manufacturing, quality control, and validation requirements and activities.</li><li>Ability to synthesize detailed information and provide clear communication and messaging across quality, manufacturing and supply chain.</li><li>English Fluent, written and spoken. Other languages are a plus.</li></ul>

Global Quality Control/Analytical Science and Technology Head

<p><strong>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.</strong></p><p>The Technology and User Services (TUS) group in NX is driven to help users use tools effectively to improve productivity and foster innovation. We deliver the Technology and User Services (TUS) group in NX to help customers use tools effectively to improve productivity and foster innovation. Our organization is here providing the technology backbone and devices that enable users to work in an office, lab or mobile environment.</p><h3><strong>QC Specialist II</strong></h3><p>This position ensures the functionality of laboratory equipment through its (re-) qualification. This includes change management, deviation handling, and the execution of compliance tasks.<br><br>This position is limited for 3 years.</p><h4><strong>Major accountabilities:</strong></h4><ul><li>Deviation handling, definition of CAPAs and Action</li><li>Change management handling</li><li>cGxP compliant review and approval of (re-) qualification activities of analytical devices (e.g. HPLCs, pH-Meter, pipettes, water baths) and release of those devices</li><li>Performance of qualification of analytical devices</li><li>Execution of compliance tasks (e.g. annual user review, periodic validation review, alarm reports)</li><li>SME in customer and health authority inspections, and DQC implementation (e.g. Empower, LabX)</li></ul><h4><strong>Essential Requirements:</strong></h4><ul><li>3-5years experience in Pharma/Manufacturing sector in analytical lab or university degree in biology, chemistry, pharmacy or any other related field</li><li>Working experience in the field of GMP production/Quality Assurance or Quality Control</li><li>Good knowledge of MS office applications and other standard IT applications and security</li><li>Risk Management, managing resources</li><li>Quality Control Sampling and Quality Control (QC) Testing</li><li>Laboratory Excellence and Innovative &amp; analytical technologies</li><li>Knowledge of TQM and related industry GxP standards and processes</li><li>Fluent English and German required</li></ul>

QC Specialist II

<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>Associate Chemist- Environment Testing - PFAS Prep- 2nd Shift, Sun - Thurs</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><h5><strong>Essential Duties and Responsibilities:</strong></h5><ul><li>Applies GMP/GLP in all areas of responsibility, as appropriate</li><li>Demonstrates and promotes the company vision</li><li>Regular attendance and punctuality</li><li>Perform prep/analysis of samples of various matrices for various analytical methods</li><li>Analyze/prep samples and QC for routine testing</li><li>Review, work up, and assemble all supporting data for work performed</li><li>Perform basic maintenance on equipment used for routine work</li><li>Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department</li><li>Prepare standard solutions and other reagents as needed</li><li>Use word processor and spreadsheet programs on PC</li><li>Dispose of all chemical wastes using approved methods</li><li>Conducts all activities in a safe and efficient manner</li><li>Performs other duties as assigned</li><li>Work overtime as workload requires</li></ul><p>Position is full-time, 2nd Shift, 2pm-10:30pm. Sun-Thurs.&nbsp; Training will be M-F, 1st Shift.&nbsp;&nbsp;</p></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>Basic Minimum Qualifications:</strong></h5><ul><li>Bachelor's Degree in Chemistry, Biology, or related field</li><li>Proficiency with computers&nbsp;</li><li>Authorization to work in the United States without restriction or sponsorship</li><li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li></ul><h5><strong>Ideal Candidates will have:&nbsp;</strong></h5><ul><li>Previous experience with sample preparation&nbsp;</li><li>Previous experience in a lab setting&nbsp;</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p><strong>Pay range: $18/hour + 10% shift differential&nbsp;</strong></p><p>Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.</p><p>As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.</p><p><i>*The benefits package offered will vary based on the employee’s full-time or part-time regular status.</i></p><p><strong>We support your development! </strong>Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><strong>We embrace diversity!</strong> Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p><strong>Sustainability matters to us!</strong>&nbsp;At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler.</p><p>Find out more in our career page: <a target="_blank" rel="noopener noreferrer" href="https://careers.eurofins.com/">https://careers.eurofins.com/</a>&nbsp;</p><p><i>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific&nbsp; agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.</i></p><p><i>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralized and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</i></p><p><i>In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.</i></p><p>All your information will be kept confidential according to EEO guidelines.</p><p><strong>Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

Associate Chemist- Environment Testing - PFAS Prep- 2nd Shift, Sun - Thurs

<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>HPLC Scientist - 2nd Shift</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><ul><li>Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products</li><li>Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, Raw Material Testing, USP, EP, JP, Compendium</li><li>Executing method transfer protocols</li><li>Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations</li><li>Reads and understands analytical procedures (compendial and client supplied) and internal SOPs</li><li>Processes data, generates reports, and evaluates data</li><li>Writes investigations</li><li>Leads project/test areas and perform method transfers/feasibility studies</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li><strong>Authorization to work in the United States indefinitely without restriction or sponsorship.</strong></li><li>Bachelor's degree in biology, chemistry, or other related degree concentration, or&nbsp;equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li><li>2+ years of previous laboratory experience&nbsp;</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p><strong>The position is full‑time and follow a 4x10 schedule, second shift, Monday through Thursday from 3:00 p.m. to 1:00 a.m.</strong></p><h5><strong>Excellent full-time benefits including:</strong></h5><ul><li>Comprehensive medical coverage, dental, and vision options.</li><li>Life and disability insurance</li><li>401(k) with company match</li><li>Paid vacation and holidays</li></ul><p><strong>Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

HPLC Scientist - 2nd Shift

<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>HPLC Empower Trainer</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><h4><strong>Job Description</strong></h4></div><div><p>Performs various training tasks in support of Biochemistry Empower Software support and training of HPLC and Capillary Electrophoresis techniques. Assist Empower Support Lead in evaluation of Empower reports and project setup. Main point person for in-lab training of all HPLC and Capillary Electrophoresis instrumentation setup and operation. Main point of contact to answer instrument setup for new analysts and best practice routines for HPLC systems and Capillary Electrophoresis Systems. Subject matter expert (SME) in chromatography and electrophoretic issues, Assists Empower Lead in development and refining of training materials. Works closely with training adminstration to schedule and execute new analyst HPLC and CE training when needed. Develop additional resources for analysts to use during instrument setup and testing.</p><h4><strong>Essential Duties and Responsibilities:</strong></h4><ul><li>Participates in training curriculum development and application</li><li>Assists training staff and management in scheduling and performing new hire HPLC and CE training to include instrument familiarity and follow-up training when required</li><li>Advises leadership on best training resources and usage of consumables for both HPLC and CE analyses</li><li>Liaise with training center to prepare departmental materials for new hire arrivals.</li><li>Maintains current resources for instrument trouble-shooting and staff training</li><li>Performs other duties as assigned</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>Basic Minimum Qualifications:&nbsp;</strong></h5><ul><li>Authorization to work in the United States without restriction or sponsorship&nbsp;</li><li>Minimum 3 years of experience in High Performance Liquid Chromatography instrumentation, Capillary Electrophoresis, and Empower Software</li></ul><h5><strong>Education/Experience:</strong></h5><ul><li>Bachelors Degree in science or related field required</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>Position is full-time, Monday-Friday 8am-5:00pm, plus additional hours, as needed. Candidates within a commutable distance of Lancaster, PA are encouraged to apply.</p><h5><strong>Excellent full-time benefits including:</strong></h5><ul><li>Comprehensive medical coverage, dental, and vision options.</li><li>Life and disability insurance</li><li>401(k) with company match</li><li>Paid vacation and holidays</li></ul><p><strong>Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

HPLC Empower Trainer

<p><strong>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</strong></p><p><strong>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</strong></p><p><strong>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</strong></p><p><strong>In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.</strong></p><h3><strong>Head of Microbiology Department (F/M)</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><h4><strong>Job Description</strong></h4></div><div><p><strong>An independent laboratory accredited in accordance with the international standard ISO/IEC 17025:2018, performing microbiological analyses of food, feed, water, and environmental samples, is seeking a new team member for the Microbiology Department.</strong></p><p>The Head of Microbiology will be responsible for leading, developing, and overseeing microbiology laboratory operations to ensure high-quality testing, full regulatory compliance, and continuous improvement. This role combines strong scientific expertise with people leadership, operational excellence, and a quality-driven mindset.</p><h4><strong>Key Responsibilities:</strong></h4><ul><li>Lead and manage the daily operations of the Microbiology department, ensuring efficiency, accuracy, and compliance with internal and external requirements.</li><li>Supervise, coach, and develop a team of microbiologists and laboratory technicians.</li><li>Completing and maintaining laboratory documentation in compliance with ISO 17025 requirements.</li><li>Review, approve, and ensure timely delivery of microbiological test results and reports.</li><li>Act as a subject matter expert for microbiological methods, investigations, deviations, and CAPAs.</li><li>Actively participate in internal and external audits and inspections, including preparation, hosting of auditors, response coordination, and implementation of corrective and preventive actions.</li><li>Oversee method validation, verification, and transfer activities.</li><li>Manage laboratory resources, including staffing, training plans, equipment, materials, and budgets.</li><li>Drive continuous improvement initiatives related to process optimization, automation, and cost efficiency.</li><li>Lead and support internal and external audits, inspections, and customer inquiries.</li><li>Ensure proper documentation, data integrity, and compliance with laboratory IT systems (eLIMS).</li><li>Collaborate cross-functionally with Quality, Operations and Customer Service teams.</li><li>Support business growth through technical expertise, customer communication, and project execution.</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Master’s degree in microbiology, Biology, Biotechnology, or a related life science.</li><li>Minimum 5 years of experience in a microbiology laboratory, with at least 2–3 years in a leadership or managerial role.</li><li>Strong knowledge of classical microbiological testing methods and molecular techniques (PCR).</li><li>Proven experience working in a regulated environment (pharma, medical devices, food, or contract testing laboratories).</li><li>Experience working in accordance with ISO 17025 standards is an advantage.</li><li>Solid understanding of quality systems, regulatory compliance, and audit readiness.</li><li>Experience with laboratory management systems (LIMS) and data integrity standards.</li><li>Excellent people management, communication, and stakeholder engagement skills.</li><li>Strong problem-solving abilities and a continuous improvement mindset.</li><li>Fluency in English and Lithuanian (written and spoken).</li><li>Quality- and compliance-focused thinking.</li><li>Customer-oriented approach.</li><li>Ability to manage multiple priorities in a fast-paced environment.</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><h5><strong>What do we offer?</strong></h5><ul><li>A leadership role in a dynamic, international laboratory environment.</li><li>Opportunities for professional growth and career development.</li><li>Competitive compensation and benefits package.</li><li>The chance to make a real impact on quality, safety, and scientific excellence.</li></ul><p><strong>We support your development!</strong>&nbsp;Do you feel like you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><strong>We embrace diversity!</strong> &nbsp;As an Equal Opportunity Employer, the Eurofins network of companies believes in strength and innovation through diversity. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p>Find out more on our Careers page: <a target="_blank" rel="noopener noreferrer" href="https://careers.eurofins.com/">https://careers.eurofins.com/</a></p><h4><strong>Company description</strong>: </h4><p>Eurofins Scientific is an international network of independent life sciences companies, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.<br>The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</p><p>In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 59 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</p><p>The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades.</p></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

Head of Microbiology Department (F/M)

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Sample collector

Academic staff

Laboratory services

Service engineer

Manager

Software

Molecular biology

Product Specialist

Application Specialist

Molecular spectroscopy UV-Vis, RAMAN, FTIR

Marketing

Analytical chemist

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

Microbiology

Liquid chromatography

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