Eurofins Lancaster Laboratories

Cell-Based Assay GMP Team Leader

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with over 6 years of relevant industry experience and supervisory experience, or;
  • Master's degree with over 5 years of relevant industry experience and supervisory experience, or;
  • PhD with 4+ years of relevant industry experience and supervisory experience.
  • Minimum of 4 years of hands-on lab experience in a GMP environment (academic-only backgrounds are not suitable).
  • Strong technical expertise in cell-based assays, ELISAs, and related workflows.

Responsibilities

  • Execute cell-based assays and ligand-binding ELISAs in a GMP lab setting.
  • Perform routine lab tasks including cell plating and 96-well plate work.
  • Assist with method qualification, transfer, and troubleshooting.
  • Ensure consistency and quality in assay execution and documentation.
  • Coordinate daily lab activities and support team workflow.
  • Provide training and guidance to junior team members.
  • Collaborate with clients and colleagues to meet project timelines and lab goals.

Benefits

  • Comprehensive medical coverage, including dental and vision options.
  • Life and disability insurance provided.
  • 401(k) plan with company matching.
  • Generous paid vacation and holidays.
Full Job Description
Join a collaborative GMP lab where your hands-on experience with cell-based assays and ELISA workflows will be put to use every day. This role is ideal for someone who enjoys staying close to the bench while also helping support and guide a small team. You'll play a key role in assay execution, method support, and day-to-day lab operations in a fast-paced environment. What You'll Do Hands-On Assay Work • Execute cell-based assays, ligand-binding ELISAs, and related workflows • Perform routine tasks such as cell plating, dilutions, and 96-well plate work • Apply strong aseptic technique and pipetting skills in a GMP setting Method & Lab Support • Assist with method qualification, transfer, and troubleshooting • Help ensure consistency and quality of assay execution Documentation & Compliance • Accurately record work in lab notebooks/e-systems • Follow GMP documentation practices and data integrity standards Team Support • Help coordinate daily lab activities and support team workflow • Provide guidance and training to junior team members as needed • Act as a go-to resource for technical questions on the team Collaboration • Work closely with clients, peers and supervisors to meet timelines and deliverables • Contribute to a positive, team-oriented lab environment Qualifications Education & Experience • Bachelor's degree with >6 years of relevant industry experience & supervisory experience, or; • Master's degree with >5 years of relevant industry experience & supervisory experience, or; • PhD with 4+ years of relevant industry experience & supervisory experience • Minimum 4 years of hands-on industry lab experience (GMP required; academic-only backgrounds are not a fit) • Strong technical background in cell-based assays, reporter-gene assays, ELISAs, 96-well plate workflows, multi-channel pipetting, cell culture, cell counting, and cell banking Leadership & Collaboration • Demonstrated leadership experience • Technical depth may offset the need for formal leadership experience • Thrives in a high-visibility, highly collaborative environment with interaction across teams and clients Communication & Work Style • Excellent written and verbal communication skills - able to handle tough questions and think on your feet • Detail-oriented, self-driven, and adaptable in a fast-paced, plate-based workflow • Strong prioritization skills with a proactive, solution-focused mindset Compliance & Documentation • Strong documentation discipline and a GMP-aligned mindset • Able to maintain accurate, audit-ready records and follow procedures consistently • Comfortable supporting audit activities and representing the team with confidence Additional Information Position is full-time, first-shift, Monday-Friday 8AM-5PM with overtime as needed. Excellent full-time benefits include: • Comprehensive medical coverage, dental, and vision options • Life and disability insurance • 401(k) with company match • Paid vacation and holidays LinkedIn: #LI-EB1

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry

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