RNA-LNP Process Development Lab Coordinator - Group Leader

At Eurofins Professional Scientific Services (PSS), we focus on your professional growth, offering opportunities to break into the biopharmaceutical industry and develop your career from the ground up. With supportive teams and tools, we invest in your development while promoting work-life balance and providing a competitive benefits package. Eurofins Scientific is an international life sciences company delivering analytical testing services to ensure safety, health, and sustainability across food, water, medicines, and more. As a global leader in testing and laboratory services, Eurofins supports genomics, discovery pharmacology, forensics, clinical studies, and advanced material sciences.

About the role

We are seeking an RNA-LNP Lab Coordinator / Group Leader to support an LNP and RNA Process Development and Technology Transfer team. The successful candidate will supervise laboratory operations, overseeing studies focused on process development and tech transfer of LNP drug products, mRNA drug substances, and gRNA drug substances. Additionally, this role involves managing GLP sample management for process development studies across multiple programs. The ideal candidate will drive efficient lab operations through excellence in inventory management, coordination of analytical testing, and clear communication of results.

Responsibilities

Technical Responsibilities

• Support continuous improvement initiatives related to lab operations.
• Build and maintain process development-specific raw material, consumable, and sample management inventory systems.
• Submit analytical samples with partner analytical organizations and track results return.
• Order supplies and equipment as needed; coordinate, receive, and inventory deliveries.
• Maintain detailed inventory records in an electronic lab notebook (ELN).
• Coordinate and ensure routine maintenance and upkeep of laboratory equipment used in process development.
• Build and maintain an equipment maintenance program for Agilent HPLC, AKTA Avant preparative liquid handling, and capillary gel electrophoresis (CGE) systems.
• Work closely with collaborators in Process Development, Tech Transfer, Facilities, Laboratory Operations, IT, and Safety teams as needed.
• Author lab maintenance protocols, SOPs, provide updates to the weekly lab operations meeting, and track and analyze lab efficiency metrics.
• Collaborate with cross-functional teams including analytical development and manufacturing.

Leadership & Team Management Responsibilities

• Lead, manage, and develop a team of process development scientists.
• Serve as a proactive and effective point of contact for client and internal teams.
• Participate in new hire interviews and onboarding processes.
• Disseminate administrative communications and promote company vision.
• Ensure adherence to the highest quality and efficiency standards in laboratory operations.
• Perform administrative tasks to support team member growth and development.
• Balance technical work with team leadership responsibilities.
• Foster morale, collaboration, and teamwork within the group.

Qualifications

Minimum Required Qualifications

• B.S. degree in biological sciences, chemistry, or biomedical/chemical engineering (or related field) with 5+ years of relevant pharmaceutical, CRO, or biotech experience.
• M.S. degree in biological sciences, chemistry, or biomedical/chemical engineering (or related field) with 3+ years of relevant pharmaceutical, CRO, or biotech experience.
• PhD with 2+ years of relevant pharmaceutical, CRO, or biotech experience.
• Prior laboratory supervisory or team lead experience.
• Excellent writing and communication skills; ability to understand and communicate scientific information.
• Experience with the operation and maintenance of equipment commonly used in the process development of nucleic acids (experience with AKTA Avant chromatography systems and Agilent HPLC systems is strongly preferred).
• Strong commitment to laboratory safety protocols.
• Attention to detail, data analysis, and troubleshooting abilities.
• Proven ability to manage multiple workstreams in parallel and adapt to changing priorities.
• Self-motivated with the ability to identify and solve problems proactively.
• Strong work ethic and excitement for leading an integrated operations team.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications

• Experience building laboratory inventory management systems is strongly preferred.
• Knowledge of nucleic acid (mRNA, gRNA), LNP, and/or biologics process development.
• Knowledge of analytical methods used for nucleic acid and/or biologics process development, including HPLC, CGE, or ELISA experience.

Schedule

Full-time, Monday-Friday, 8am-5pm with overtime as needed.

Benefits

• Comprehensive medical, dental, and vision coverage.
• Life and disability insurance.
• 401(k) with company match.
• Paid vacation and holidays.
• Eligibility for yearly goal-based bonus & merit-based increases.

Pay

$100,000 to $115,000 per year based on education and related experience.

Candidates living within a commutable distance of Boston, MA are encouraged to apply.