Downstream Process Development Group Leader

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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.

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.

If you’re looking for a rewarding career, a place to call home, apply with us today!

The Downstream Process Development Group Leader will lead a team of scientists and analysts in executing small-scale purification studies to support biopharmaceutical manufacturing processes. This role combines hands-on technical expertise with leadership responsibilities, ensuring high-quality data generation, documentation, and cross-functional collaboration. The Group Leader will drive innovation, manage project timelines, and support technology transfer activities.

Key Responsibilities:

Technical Responsibilities:

• Perform small-scale purification studies including chromatography, ultrafiltration/diafiltration (UF/DF), TFF, and sterile/depth filtration.
• Prepare and operate chromatography systems (e.g., AKTA) for experimental purification runs.
• Conduct basic lab support tasks such as solution preparation, sample submission, and equipment calibration.
• Statistically analyze large datasets and draft comprehensive technical reports to support study outcomes.
• Present technical findings during cross-functional meetings and contribute to scientific discussions.
• Lead purification efforts for assigned projects, including planning, execution, and documentation.
• Coordinate lab activities with broader scientific teams to ensure alignment and efficiency.
• Ensure compliance with GxP standards, GHS policies, and all written procedures and protocols.
• Balance multiple projects and tasks, prioritize effectively, and communicate progress across teams.

Leadership Responsibilities:

• Supervise and support a team of analysts, ensuring timely execution of work assignments.
• Participate in candidate interviews and contribute to hiring decisions.
• Lead onboarding and training of new employees; provide ongoing mentorship and development.
• Conduct performance reviews and deliver constructive feedback to team members.
• Monitor team workload and ensure proper time management and resource allocation.
• Engage in leadership development training and promote a culture of continuous improvement.

Education & Experience:

• Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 3+ years of relevant industry experience, or Master’s degree with 1+ years of experience.
• Hands-on experience with downstream purification processes in a pilot-scale or R&D setting.
• Familiarity with AKTA chromatography systems and Unicorn software preferred.

Technical Skills:

• Strong documentation and organizational skills.
• Proficient in lab equipment operations and data interpretation.
• Experience troubleshooting downstream processing activities (e.g., chromatography, UF/DF, filtration).
• Practical experience with scale-up, technology transfer, and GMP manufacturing support.
• Knowledge of upstream processing is a plus.
• Experience with software tools such as Solo VPE, JMP, Viper, BioSMB, PALL System Software, Pendotech, and Microsoft Office.

Additional Qualifications: 

• Excellent communication and time management skills.
• Ability to work in both collaborative (60%) and independent (40%) environments.
• Capable of lifting/pushing up to 75 lbs, standing for extended periods, and working on platforms or ladders.
• Authorized to work in the United States indefinitely without restriction or sponsorship.

Position is Full Time, Monday-Friday, First Shift, Monday through Friday from 8 am-4:30 pm Candidates currently living within a commutable distance of Framingham, MA, are encouraged to apply

Excellent full-time benefits include: 

• Medical Coverage: Comprehensive medical insurance options
• Dental & Vision: Full dental and vision coverage available
• Life & Disability Insurance: Employer-sponsored plans
• Retirement: 401(k) plan with company match
• Paid Time Off: Vacation days, paid holidays, and additional PTO options
• Compensation: $42.00 - 47.00 per hour
  • $87,360–$97,760 annually 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.