<p>Company Description</p> <p>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.</p> <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 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.</p> <p>If you're looking for a rewarding career, apply with us today!</p> <p>Job Description</p> <p>We are seeking an experienced professional with a strong background in analytical method development and technology transfer within a GMP-regulated environment. This role primarily supports our client by performing routine GMP sample testing, method validation, and bioassay execution. In addition to technical responsibilities, this individual will serve as a group leader, overseeing a team of Eurofins PSS employees embedded within the client's operation.</p> <p>Primary Responsibilities:</p> <ul> <li>Perform complex GMP release and stability assays, including cell-based functional assays such as PCR, ELISA, and NGS. </li><li>Support method transfer, qualification, and validation of bioassays for lot release and characterization of cell and gene therapy products and critical materials. </li><li>Author and review SOPs, technical reports, and other documentation in compliance with regulatory standards. </li><li>Collaborate with cross-functional teams on method development, product/process characterization, comparability studies, and technical investigations. </li><li>Analyze, trend, and interpret data to assess and maintain consistent assay performance and method robustness. </li></ul> <p>Leadership Responsibilities:</p> <ul> <li>Supervise and support the daily performance of the Eurofins PSS team. </li><li>Assist in the recruitment and onboarding of new team members. </li><li>Communicate administrative updates and reinforce company vision and values. </li><li>Ensure high standards of quality, efficiency, and GMP compliance in all laboratory operations. </li><li>Manage shift coverage, scheduling, and resource allocation. </li><li>Support employee growth through performance discussions and development planning. </li><li>Maintain a balanced role between hands-on technical work and leadership duties. </li><li>Cultivate a positive team culture, encouraging collaboration, accountability, and continuous improvement. </li></ul> <p>Qualifications</p> <ul> <li>Bachelor's degree in a scientific discipline with 3-8 years of relevant experience, or a Master's degree with 2-5 years of experience. </li><li>Proven experience in analytical method validation in alignment with GMP regulations. </li><li>Demonstrated success in the transfer of analytical methods into GMP-regulated laboratories. </li><li>Hands-on experience performing routine sample testing in a GMP environment. </li><li>Strong knowledge of regulatory expectations related to method lifecycle management (e.g., FDA, EMA). </li><li>Excellent written and verbal communication skills; able to work collaboratively within cross-functional teams. </li><li>Self-motivated, highly organized, and detail-oriented with strong problem-solving capabilities. </li><li>Previous laboratory supervision or leadership experience is preferred. </li><li>Experience with potency assays (e.g., cell-based assays, ELISA) is a plus.. </li><li>Authorization to work in the United States indefinitely without restriction or sponsorship </li></ul> <p>Additional Information</p> <p>The position is full-time and permanent, Monday-Friday, 8 am-5 pm, with overtime as needed. Candidates living near or in Cambridge, MA, are encouraged to apply.</p> <p>Excellent full-time benefits include:</p> <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>Eurofins Lancaster Laboratories Professional Scientific Services (PSS) is a global, award-winning insourcing solution that places our people at our clients' sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.</p> <p>We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients' quality systems and equipment.</p> <p>To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.</p> <p>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</p>