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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>Quality Assurance Manager</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><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>The <strong>Quality Assurance Manager </strong>(QAM) oversees QA compliance at the laboratory. The QAM ensures that company policies, procedures, and implementation of a robust and effective Quality System is maintained. This includes identifying or developing quality management tools, assessing risks and leading root cause investigations, evaluating company-wide trends for weaknesses and opportunities to advance the company’s leadership position in the environmental industry, and training quality staff in the implementation of Quality Systems, techniques, and tools. The QAM will also work with various accrediting bodies to maintain our many state and program certifications.</p><h4><strong>Quality Assurance Manager responsibilities include, but are not limited to, the following:</strong></h4><ul><li>Ensure adherence to highest quality and efficiency standards in laboratory operations</li><li>Lead team, schedule, and train employees; ensure coverage and performance; foster morale and teamwork</li><li>Lead interventions in laboratories with inadequate Quality Systems or management</li><li>Review assigned laboratories’ monthly reports to stay current with laboratory issues and achievements</li><li>Review audit responses for assigned laboratories as needed Compile Quality System metrics to monitor the status and performance of assigned laboratories</li><li>Monitor laboratory certification activities to ensure no major losses of certifications Investigate issues raised by clients, QA, sales, and other departments to find root cause, implement corrective action, and document proper response</li><li>Perform internal investigations of suspected data integrity related and/or ethics violation issues</li><li>Provide review and comments on state, client, TNI, and federal agency programs and requirements</li><li>Monitor regulatory and accreditation activities for business opportunities and threats</li><li>Research Quality Systems information and stay abreast of new practices to maintain knowledge to provide guidance for the laboratory site.&nbsp;</li><li>Participate in environmental industry committees or organizations to contribute to industry-wide initiatives that can impact the company Identify and/or develop model Quality System tools, policies, and procedures, and make these available for adoption within the laboratories</li><li>Develop and participate in the Quality Management Training for new and prospective quality management staff Coordinate quality assurance and technical training courses, as applicable</li><li>Assist Laboratory Directors/BUMAs in QA personnel decisions including: staffing, hiring, evaluations, and disciplinary actions as requested</li><li>Attend meetings to stay current with industry trends and QA programs</li><li>Participate in the Laboratory Information Management System (LIMS) oversight and standardization Assist with internal Quality Systems Audits as needed</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>The ideal candidate would possess the following skills and knowledge:</strong></h5><ul><li>Strong leadership, initiative, and teambuilding skills</li><li>Knowledge of environmental laboratory accreditation requirements</li><li>Quality Assurance and Quality Control principles</li><li>Statistics and the fundamental application in an environmental laboratory</li><li>Root cause analysis and corrective action principles</li><li>Change management techniques and group dynamics</li><li>Knowledge of environmental chemistry, regulatory methods and accreditation requirements, and instrumental techniques</li><li>Experience with laboratory operations</li><li>Strong analytical, logical, and negotiating skills</li><li>Strong interpersonal skills and leadership abilities</li><li>Ability to handle multiple priorities</li><li>Strong computer, scientific, and organizational skills</li><li>Excellent communication (oral and written) skills and attention to detail</li><li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li><li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li></ul><h5><strong>Basic Minimum Qualifications:</strong></h5><ul><li>BS degree in a science, combination of QA experience and knowledge of the environmental testing industry may substitute for a degree.</li><li>Minimum 5-10 years of environmental laboratory experience and 5 years QA experience.&nbsp; Advanced degree may substitute for experience.</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li><li>Professional working proficiency in English is required, including the ability to read, write, and speak in English.</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><ul><li><strong>Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with additional time as needed.&nbsp;</strong></li><li><strong>Position is located at our Tinley Park, IL location.&nbsp;</strong></li><li><strong>Position Pay Range is $65,000- $80,000 target range but will be reviewed based on experience.&nbsp;</strong></li></ul><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! </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> We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!</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><strong>Eurofins USA Environment Testing 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></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>

Quality Assurance Manager

<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>QC Laboratory Technician</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><p><strong>This is a full time, permanent position. Shift work is required for this role, Working a biweekly rotating shift pattern, which is: 08:30 – 20:30 Week 1: Monday, Tuesday, Friday, Saturday &amp; Sunday. Week 2: Wednesday &amp; Thursday.</strong></p><p>As a QC Laboratory Technician you will provide laboratory support services relating to water sampling, operating waste and parts autoclaves and performing a clean on a QC Lab area simulating an ISO-graded clean room under the customer quality system, using customer company procedures, and while adhering to Eurofins general policies and standards.</p><h4><strong>Job Responsibilities that you be covering:</strong></h4><ul><li>As a QC Laboratory Technician you will support laboratory analytical personnel by carrying out ad‑hoc laboratory duties, including water sampling in grey space areas and assisting with laboratory investigations as required.</li><li>You will be responsible for the accurate and timely logging of samples, ensuring all laboratory documentation and records are completed “Right First Time” and maintained to the required quality and GMP standards.</li><li>As a QC Laboratory Technician you will manage the day‑to‑day operation of autoclaves, including load preparation, periodic checks, validated load patterns and ensuring equipment operates correctly in line with approved procedures.</li><li>As a QC Laboratory Technician you will maintain high standards of cleanliness and housekeeping across the laboratory, CTU and associated equipment, carrying out routine, periodic and ad‑hoc cleans in ISO‑graded cleanroom‑simulated environments.</li><li>You will actively participate in required training, complete and maintain training records to an appropriate standard, and support the training of other team members when instructed.</li><li>As a QC Laboratory Technician you will operate with a strong customer focus, adhering to safety, quality and housekeeping standards, escalating anomalies or non‑conformances promptly, responding to customer queries, and contributing to continuous improvement initiatives.</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>What skills, qualifications and experiences you will hold as a QC Laboratory Technician:</strong></h5><ul><li>As a QC Laboratory Technician you will hold a relevant scientific qualification, ideally degree or diploma level, in a suitable discipline, providing a strong foundation in laboratory science.</li><li>You will demonstrate effective planning and organisational skills, enabling you to manage your workload efficiently while meeting defined timelines and quality standards.</li><li>As a QC Laboratory Technician you will show a high level of accuracy and attention to detail, ensuring laboratory activities, analytical data and documentation are completed right first time.</li><li>As a QC Laboratory Technician you will be a positive and reliable team player, contributing to a collaborative, high‑performing laboratory environment aligned with Eurofins values.</li><li>You will possess strong IT and documentation skills, supporting accurate data entry, record‑keeping and effective use of laboratory systems.</li><li>As a QC Laboratory Technician you will communicate clearly and professionally with internal and external stakeholders and have familiarity with pharmaceutical or laboratory operations, including GMP, documentation, autoclaves and sample management, with GMP experience considered an advantage.</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events.</p><h4><strong>As a Eurofins employee you will benefit from:</strong></h4><ul><li>We offer exceptional opportunities for career growth, within a friendly and supportive team. As well as a competitive salary, pension and associated benefits you will enjoy an unrivalled working environment, including an active social calendar and subsidised canteen, all while working in a start of the art client facility- a leading biotechnology company</li><li>Fantastic developmental opportunities and career progression pathways such as leadership, training, compliance and Subject Media Expert.</li><li>Full Benefits Package including:-<ul><li>Pension</li><li>Private Medical Insurance</li><li>Income protection and life assurance</li><li>Annual discretionary bonus</li><li>Birthday Holiday entitlement</li></ul></li><li>Exciting Eurofins Incentives: Employee Activity Committee (EAC), Equality Driving Excellence (EDE), significant Reward and Recognition programme Opportunity to benefit from Eurofins Operational Development training platform, plus potential support for part-time training (relevant to the position)</li><li>Full use of the canteen facilities and barista on the client site</li><li>Free parking onsite and onsite electric charging</li><li>Additional annual leave days with continued service</li><li>The opportunity to work on life saving products</li></ul><h4><strong>What Happens Next</strong></h4><p>Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths.</p><h4><strong>Your data</strong></h4><p>As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.</p><p>We embrace diversity! 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>For more information about Eurofins PSS® please visit our </strong><a target="_blank" rel="noopener noreferrer" href="https://www.eurofinspss.com/ie/"><strong>website </strong></a><strong>and watch a message below from our Global Head, Beth Di Paolo.</strong></p></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

QC Laboratory Technician

<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>QC Analyst</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><p>For our team in Nijmegen, we are looking for an enthusiastic QC Analyst. This is a unique opportunity to join a team in a dynamic environment where your contributions to the QC team will have a direct impact on helping patients worldwide access a highly innovative new product.</p><p>This role drives the accuracy and reliability of our products by performing QC testing, maintaining the QC laboratory, and ensuring compliance with regulatory standards. You’ll be part of the Quality Control team, collaborating with manufacturing, compliance, and cross-functional colleagues to deliver high-quality results and continuous improvement. This is an on-site role with evening shift flexibility.</p><h4><strong>Tasks and Responsibilities:</strong></h4><ul><li>Perform maintenance and calibration of HPLC equipment and general laboratory instruments.</li><li>Ensure the cleanliness, organization, and maintenance of the laboratory.</li><li>Conduct analytical tests, for example: HPLC, pH measurements, Size Exclusion Chromatography (SEC), Bio Burden tests, and Particle Distribution Analysis (PDA).</li><li>Responsible for conducting and interpreting NMR analyses.</li><li>Inspect and verify labels and incoming goods to ensure compliance with specifications and quality standards.</li><li>Document and report results according to standardized protocols and guidelines</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Bachelor’s degree in Chemistry or related sciences;</li><li>2-3 years experience in Quality or Quality Control is required;</li><li>Experience with NMR, preferably with polymers;</li><li>Experience with HPLC;</li><li>Experience in a pharmaceutical environment and knowledge of GxP is preferred;</li><li>Willingness to work flexible hours, including occasional evening shifts, is essential.</li><li>You enjoy working in a team and communicate well;</li><li>You are accurate, and have great attention to detail;</li><li>You can work independently;</li><li>You are a quick learner who thrives in a dynamic environment;</li><li>You are self-motivated with a positive attitude;</li><li>You enjoy volunteering your ideas and working on continuously improving your environment.</li><li>You are fluent in English (Spoken/written</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>Working at PSS means working with highly motivated people with a can-do mentality. Our people work in an international environment, within an enthusiastic team and for an organization where there is sufficient room to develop further. Working together is extremely important to us and having fun in what you do is part of that! Our monthly team lunches, team activities and the hand out of awards to our colleagues are an example of this. We also offer:</p><ul><li>A responsible and challenging position within the team;</li><li>Plenty of room for your own ideas and input;</li><li>Specialist training and a range of opportunities for personal and professional development;</li><li>Online preventive mental health platform;</li><li>Flexible working hours;</li><li>Good salary and benefits.</li></ul><p>Working at PSS offers you the flexibility and personal touch of working in a medium sized and dynamic company, whilst also allowing you to benefit from having Eurofins as a parent company. Our ambitious growth plans provide ample opportunities for the motivated employees:</p><ul><li>Plenty of opportunities for growth;</li><li>Varied work where you are in regular contact with other companies and scientists within the Eurofins group;</li><li>A broad customer portfolio ensuring a lot of diversity in your work.</li></ul><p><strong>Would you like to know more?</strong><br>For questions regarding the position, please follow the link below ‘I’m interested’ in order to contact the hiring manager.</p><p><strong>Acquisition for this vacancy is not appreciated.</strong></p></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

QC Analyst

<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>Entry Level Quality Assurance Technician - 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><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><section><div><div><section><div><h4><strong>Job Description</strong></h4></div><div><h5><strong>Primary responsibilities include, but are not limited to, the following:</strong></h5><ul><li>Collect samples from the operating areas of the facility</li><li>Log samples into the laboratory info management system</li><li>Perform routine sample prep and analysis</li><li>Perform routine instrument maintenance</li><li>Complete calibration/verification activities and documentation for instrumentation under Factory QA control</li><li>Upload collected analytical data to the laboratory information management system or designated system</li><li>Perform general cleaning of the laboratory benches and Factory QA work areas</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><h5><strong>The Ideal Candidate would possess:</strong></h5><ul><li>Dependable and punctual</li><li>Ability to work both in a team environment and independently</li><li>Ability to work flexible hours as needed</li><li>Ability to work overtime/weekends</li><li>Ability to lift over 50 lbs.</li><li>Ability to be on feet over 50% of the shift</li><li>Professional approach to work, detail oriented</li><li>Flexible skills, able to manage multiple tasks</li><li>Basic computer skills (Windows, MS office, LIMS, etc.)</li><li>Excellent communication skills</li><li>Good troubleshooting/problem solving skills</li><li>Comply with all Safety, Regulatory, and Good Manufacturing Practices (GMPs).</li><li>Self-motivated</li><li>Candidates within a commutable distance of Nashville, TN are encouraged to apply</li></ul><h5><strong>Minimum Qualifications:</strong></h5><ul><li>High School Diploma or Equivalent</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><h5><strong>What we offer:</strong></h5><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><li>Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.</li></ul><p>We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.</p><p>#LI-LW1&nbsp;</p><p>Position is full-time 2nd shift, 2:00 PM - 10:30 PM.&nbsp; Candidates currently living within a commutable distance of Nashville, TN are encouraged to apply.</p><p><strong>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employe</strong></p></div></section></div></div></section></div></section></div></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

Entry Level Quality Assurance Technician - 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>Quality Control Analyst&nbsp;</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><section><div><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><p><strong>Unfortunately, we are unable to offer sponsorship for this role.&nbsp;</strong></p><p>The purpose of this role is to&nbsp;support the Operations Team in the application and ongoing compliance of Eurofins Linlithgow Quality Systems, providing quality control oversight and support across all departments.</p><p><strong>This position is to cover 40 hours a week - Monday to Friday from 08:30 till 17:00. There may be option for this role to fit two part time roles for the right candidates.&nbsp;</strong></p><ul><li>Carry out routine quality control checks to support day-to-day laboratory operations and ensure compliance with internal procedures and accreditation requirements.</li><li>Perform and document equipment calibrations, verification checks, and associated record keeping to maintain confidence in results and equipment performance.</li><li>Prepare internal quality control (QC) materials and samples, ensuring correct preparation, traceability, storage, verification, and labelling.</li><li>Organise Proficiency Testing (PT) testing as required, ensuring results are generated and submitted in line with deadlines and quality expectations.</li><li>Complete environmental monitoring activities in line with site quality requirements, recording results accurately and escalating deviations where necessary.</li><li>Maintain training records and quality documentation, supporting competence, traceability, and audit readiness.</li><li>Investigate customer complaints relating to quality and laboratory output, supporting fact-finding, evidence gathering, and corrective actions where required.</li><li>Investigate Non-Conforming Work (NCWs), ensuring issues are documented clearly, actions are progressed, and learning is captured appropriately.</li><li>Participate in root cause analysis activities (e.g., 5 Whys / Fishbone), supporting effective corrective and preventative actions.</li><li>Support method development activities where required, contributing to improvement, optimisation, and controlled implementation into routine use.</li><li>Support method validation work, ensuring required testing, documentation, and evidence is generated in line with quality standards and accreditation expectations.</li><li>Carry out hygiene checks and audits, reporting findings and supporting corrective actions and follow-up.</li><li>Support and participate in test witness audits, ensuring readiness, compliance, and completion of any required actions.</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Educated to HNC/HND level (or equivalent) in a science-related discipline, or able to demonstrate equivalent relevant experience in a laboratory / QC environment.</li><li>Good understanding of Quality Control requirements and laboratory QC processes, including routine checks, calibration requirements, and data/record integrity.</li><li>Awareness of working within a regulated laboratory environment with a strong focus on compliance, traceability, and accurate documentation.</li><li>Previous experience in a QC or QT role, ideally within a laboratory setting. Both Microbiology and chemistry.</li><li>Experience following controlled procedures, maintaining records, and working to agreed turnaround times and priorities.</li><li>Demonstrable experience supporting investigations (e.g., complaints, non-conforming work, deviations) and escalating issues appropriately.</li><li>ompetent IT skills, including the ability to use laboratory systems and Microsoft Office effectively.</li><li>Good working knowledge of Excel (data entry, formatting, basic formulas, filtering/sorting, and maintaining accurate records).</li><li>Ability to manage and maintain QC documentation and records accurately, ensuring traceability and version control.</li><li>Strong attention to detail and a commitment to producing accurate, high-quality work.</li><li>Professional and approachable manner with the ability to build effective working relationships across departments.</li><li>Clear communication skills (written and verbal), with confidence liaising with operational teams and escalating issues where required.</li><li>Ability to prioritise workload effectively and remain organised in a fast-paced environment.</li><li>Flexible and proactive approach, with a willingness to support wider business needs when required.</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p>At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities.</p><h4><strong>As a Eurofins employee you will benefit from:</strong></h4><ul><li>Additional Annual Leave at Employees set service dates &nbsp;&nbsp;</li><li>Company Pension Plan</li><li>Life Assurance Scheme (4 times annual salary)</li><li>Healthcare Cash Plan (6+ months service)</li><li>Enhanced Maternity, Adoption and Paternity Schemes</li><li>Employee Assistance Programme – 24/7 confidential</li><li>Health and Wellbeing Programmes</li><li>Free parking</li><li>Worldwide career opportunities</li><li>We also have in place rewards recognising the great work our&nbsp;employees deliver, their dedicated service and celebrating special life events.</li></ul><h4><strong>What Happens Next</strong></h4><p>Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths.&nbsp;</p><h4><strong>Your data&nbsp;</strong></h4><p>As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.<strong>&nbsp;</strong></p><h4><strong>Closing Date</strong></h4><p>We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible.</p><p>Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful.&nbsp;</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&nbsp;embrace&nbsp;diversity!</strong>&nbsp;Eurofins network of companies believe in strength and innovation through diversity, being an&nbsp;<u>Equal Opportunity Employer</u>. 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></div></section></div></section></div></section></div></section></div></div></section></div></section></div></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

Quality Control Analyst 

<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>Stability Specialist</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><ul><li>Receive, store, forecast, submit, and deliver stability and analytical samples</li><li>Understands and follows all relevant policies relating to this job including business, compliance, quality, environmental and safety expectations</li><li>Supports the development, registration and launch of new pharmaceutical products</li><li>Conduct annual inventory of stored material</li><li>Build and maintain stability studies in Lab Information Management System (LIMS)</li><li>Support the client's work requests as needed&nbsp;</li><li>Support domestic and international shipping of material</li><li>Additional duties as needed</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Fundamental knowledge of cGMP compliance requirements</li><li>Excellent communication (oral and written) and attention to detail</li><li>Strong computer and organizational skills and experience with Microsoft Office</li><li>Ability to work independently and as part of a team, have self-motivation, adaptability, and a positive attitude</li><li>Ability to learn new techniques, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies</li><li>Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements&nbsp;</li></ul><h4><strong>Minimum Qualifications:</strong></h4><ul><li>Bachelor's degree</li><li>2 years professional experience</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><ul><li>The position is full-time, Monday through Friday, &nbsp;8am-5 pm</li><li>May be requested to work on weekends, overtime, and holidays based on business needs.</li><li>Candidates currently living within a commutable distance of Indianapolis, IN&nbsp;<strong>&nbsp;</strong>are encouraged to apply.</li><li>Ability to work overtime as required.</li><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><li><strong>#LI-EB1</strong></li></ul><p><strong>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></div></section></div></section></div></section></div></section></div></div></section></div></section></div></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

Stability Specialist

<p><strong>At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic &amp; consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.</strong></p><p><strong>PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.</strong></p><p><strong>Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.</strong></p><h3><strong>QC Lab Chemistry Sampling Associate - Entry Level</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><section><div><p><strong><u>What You’ll Do</u></strong></p><ul><li>Perform hands‑on sampling and testing of compressed gas systems and tankers</li><li>Work inside cleanrooms to dispense raw materials and inspect containers</li><li>Receive, handle, label, and dispose of samples safely and accurately</li><li>Calibrate or verify calibration of instruments before use</li><li>Record test results with precision and flag any unusual findings</li><li>Keep lab supplies stocked and maintain a clean, organized workspace</li><li>Deliver excellent service to internal clients and manufacturing partners</li><li>Complete required training and stay current on procedures and regulations</li><li>Follow all regulatory and safety requirements in a GMP‑aligned environment</li></ul><p><strong><u>Opportunities You’ll Gain</u></strong></p><ul><li><strong>Grow your technical skills</strong>&nbsp;through cross‑training in pH, Conductivity, Nitrate ID, TOC, and Appearance testing</li><li><strong>Build cleanroom experience</strong>&nbsp;— a highly valued skill in biotech and pharmaceutical manufacturing</li><li><strong>Develop professional discipline</strong>&nbsp;working in regulated environments with clear procedures and expectations</li><li><strong>Strengthen your resume</strong>&nbsp;with calibration, testing, and quality‑focused responsibilities</li><li><strong>Be part of a team</strong>&nbsp;that supports critical biopharmaceutical manufacturing operations</li></ul><p><strong><u>Work Environment</u></strong></p><p>This is a fully onsite, lab‑based role in biopharmaceutical cleanrooms and laboratory spaces. You’ll spend significant time in&nbsp;<strong>ISO 8 cleanrooms</strong>, which require specific gowning and hygiene standards:</p><ul><li><i>No cosmetics (makeup, false lashes, spray tans, etc.)</i></li><li><i>Short, unpolished nails</i></li><li><i>No jewelry (except medical alert items or a simple band that fits under gloves)</i></li><li><i>Hair must be fully contained in a hairnet; facial hair must be neatly trimmed and coverable</i></li></ul><p>These standards help protect product quality and ensure a safe, controlled environment.</p></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><p><strong><u>Ideal Qualifications</u></strong></p><ul><li>Brings a positive, adaptable, team‑focused attitude with strong attention to detail</li><li>Learns new techniques quickly and follows procedures accurately</li><li>Communicates clearly in both writing and conversation</li><li>Comfortable in a moderately physical role that involves standing for extended periods</li><li>Organized, computer‑proficient, and able to work reliably in a structured environment</li></ul><p><strong><u>Minimum Qualifications</u></strong></p><ul><li>Bachelor’s degree in chemistry or a related scientific field,&nbsp;<strong>or</strong>&nbsp;equivalent hands‑on experience</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><ul><li>Hourly pay range: $21.50 - $22.50&nbsp;</li><li>Schedule: Monday - Friday, 8:00 AM - 4:30 PM&nbsp;</li><li>LinkedIn: #LI-EB1</li></ul><p><strong>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

QC Lab Chemistry Sampling Associate - Entry Level

<p><strong>Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilizing their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!</strong></p><h3><strong>Method Development &amp; Validation Specialist</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><h4><strong>Job Description</strong></h4></div><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><ol><li>Collect information required for the analytical target profile from Project (analytical lead, project manager, product owner…).</li><li>Propose and test candidate analytical techniques potentially able to meet expected needs.</li><li><strong>Develop robust &amp; efficient analytical methods by aQBD using classical LC-UV method</strong>&nbsp;with no/limited assistance utilizing modern &amp; state‑of‑the‑art statistical approaches to bring them to successful validation.</li><li>Collect data from development and take decisions / propose solutions based on obtained results. Prepare support and present development status in technical team review meetings.</li><li>Assure that complex technical data are reported with scientific excellence and communicate the outcome of the analytical activity to team/supervisor/customer.</li><li>Understand and master all regulatory requirements pertaining to analytical method performance.</li><li>Contribute and/or collaborate to analytical method validation/co-validation/transfer both internally or external labs.</li><li>Design complex study designs and write associated Quality documents (protocols, reports, procedures).</li><li>Document results in laboratory notebooks according to established GDP procedures.</li><li>Advise supervision and customer when facing issues and propose options to meet timeline/define new timeline.</li><li>Participate in method comparability/equivalence studies to enable continuation of the analytical method lifecycle.</li><li>Interact with cross‑functional teams of analytical experts with internal/external labs/suppliers.</li><li>Identify risks, issues and opportunities and communicate to supervisor and customer.</li><li>Collaborate to investigations in complex analytical issues corresponding to atypical or out‑of‑specification/trend test results and instrumentation/methodology issues.</li></ol></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Holds a master’s degree in chemistry/Analytical chemistry or a similar field.</li><li>We are looking for candidates who have more than 4 years of experience.</li><li>Strong technical knowledge of various analytical techniques, especially Liquid Chromatography (LC-UV) with significant experience in development validation/verification/transfer and troubleshooting.</li><li>Understanding of interactions with other disciplines: Formulation, Process Development, Regulatory Affairs, QA.</li><li>Strong knowledge of compendial and other applicable regulations.</li><li>Fluent communication skills in English; French is nice to have.</li><li>Basic project management skills.</li><li>The candidate must show Ownership, critical mindset and out of the box thinking.&nbsp;</li><li>Ability to operate in certified environments.</li><li>Eagerness to learn new analytical techniques.</li><li>Knowledge of new analytical strategies (ICH Q14, QbD…).</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><ul><li>A full-time (40hours/week) Monday – Friday job.</li><li>Job location: Braine l'alleud</li><li>A Permanent contract with flexible working hours.</li><li>Work in a fast-growing international organization.</li><li>Meal Vouchers 8 Euro/Working Day.</li><li>Eco-Cheques +/- 250 Euro/Year.</li><li>DKV Hospitalization insurance.</li><li>Additional 12 ADV days.</li><li>A company well-being program targeting both mental and physical well-being.</li><li>A fantastic team with monthly team lunches, fun teambuilding activities (laser tag, escape rooms, sports, etc.) and above all; a great collaborative international work environment.</li><li>Personal development through learning on the job and additional trainings.</li></ul></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

Method Development & Validation Specialist

<p><strong>The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.</strong></p><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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.</strong></p><p><strong>If you’re looking for a rewarding career, apply with us today! &nbsp;</strong></p><h3><strong>Analytical Science Clinical Data Review Supervisor</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><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><h4><strong>Job Description</strong></h4></div><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><p>The Analytical Science Clinical Data Review Supervisor is responsible for supervising clinical laboratory data review activities, ensuring data integrity, regulatory compliance, and timely delivery of results. This role leads and develops QC data review teams while coordinating training, investigations, and process improvements to support high-quality analytical science operations.</p><p><strong>Key Responsibilities</strong></p><p><strong><u>Laboratory &amp; Clinical Data Review Responsibilities</u></strong></p><ul><li>Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and procedural requirements.</li><li>Coordinate and support the implementation of laboratory process and safety improvements.</li><li>Review laboratory logbooks and records for completeness, accuracy, and regulatory compliance.</li><li>Verify chain of custody integrity for all tested samples.</li><li>Review audit trails to confirm actions were executed appropriately and within timelines defined by governing procedures.</li><li>Partner with testing teams to resolve data discrepancies, corrections, and annotations to ensure compliance standards are met.</li><li>Conduct laboratory investigations, including root cause analysis, and prepare clear, compliant investigation reports.</li><li>Review and verify both paper and electronic laboratory data.</li><li>Perform data review for Clinical Routine and Process Sciences testing, including compendial assays, ELISA, gel electrophoresis, and HPLC.</li><li>Communicate routine deliverables, status updates, and findings to appropriate internal and client-facing teams.</li><li>Utilize the Laboratory Information Management System (LIMS) to track samples, results, investigations, and performance metrics.</li></ul><p><strong><u>Supervisory &amp; Leadership Responsibilities</u></strong></p><ul><li>Supervise direct reports, group leaders, and technical teams within a clinical laboratory environment.</li><li>Promote and model the company’s vision, values, and culture of quality.</li><li>Coordinate and participate in hiring, interviewing, and selection activities.</li><li>Oversee staff scheduling, workload distribution, and onboarding of new hires.</li><li>Manage overtime and weekend schedules to meet operational and client needs.</li><li>Develop and implement team-building initiatives to support engagement and performance.</li><li>Apply Lean and continuous improvement principles to optimize data review workflows.</li><li>Supervise daily operations of the Quality Control (QC) clinical data review team.</li><li>Coach, mentor, and support group leaders while monitoring productivity and quality performance.</li><li>Support ongoing professional development and career growth of team members and group leaders.</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><ul><li>Bachelor’s degree in Chemistry, Life Sciences, Engineering, or a related scientific discipline.</li><li>Minimum of 3 years leading dynamic teams in technical or laboratory settings, with a strong emphasis on team development, coaching, and performance management.</li><li>At least 3 years of hands-on laboratory experience; prior work in a GMP-regulated environment is strongly preferred.</li><li>Experience with HPLC, MCE, and/or ELISA data strongly preferred</li><li>Experience with chromatography processing and review of logbooks, electronic lab notebooks, and LIMS</li><li>Demonstrated experience managing day-to-day lab operations, including workflow optimization, equipment oversight, and compliance with safety and quality standards.</li><li>Proven ability to serve as a liaison between internal teams and external clients, ensuring effective communication, timely project execution, and high client satisfaction.</li><li>Authorization&nbsp;to work in the United States indefinitely without restriction or sponsorship</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4><p><strong>What to Expect in the Hiring Process:</strong></p><ul><li>10-15 Minute Phone Interview with Regional Recruiter</li><li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li><li>30 Minute In-Person Onsite Meeting with the Team</li></ul><p>This is a full-time, <strong>100% onsite</strong> position based on a first-shift schedule (Monday–Friday, 8:30am–4:30pm), with overtime required as needed. Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply.</p><p><strong>What We Offer:</strong></p><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><li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li><li>Hourly compensation is between $38.00 - $41.00 per hour, depending on education and experience&nbsp;</li></ul><p><strong>Eurofins USA PSS Insourcing Solutions 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></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></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>

Analytical Science Clinical Data Review Supervisor

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