QC Bioassay Specialist - Norwood - Randstad

    Randstad
    Randstad Norwood

    1 day ago

    Pharmaceutical / Bio-tech
    Description

    Elevate the Future of Medicine: QC Bioassay Specialist (2nd Shift)

    Are you a Bioassay expert with a "Right First Time" mentality? We are looking for a high-performing Quality Control Specialist to join a fast-paced, cutting-edge manufacturing facility in Norwood, MA. This isn't just a bench role; it's a chance to act as a Subject Matter Expert (SME), leading method transfers and mentoring the next generation of analysts in a cGMP environment.

    What's In It For You?

    Step into a role where your technical expertise directly impacts the delivery of life-changing medicines. You'll enjoy the stability of a Monday–Friday schedule while reaping the rewards of a 10% shift differential, boosting your earning potential from day one. This 6-month contract is designed for growth, offering a clear pathway for extension or permanent conversion based on your performance. You'll work in a state-of-the-art facility, collaborating with elite cross-functional teams to solve complex analytical challenges and sharpen your leadership skills.

    The Role

    As a Specialist in the QC Bioassay lab, you will be the bridge between development and routine testing. You won't just follow protocols—you'll write them, troubleshoot them, and ensure every drug substance meets the highest regulatory standards.

    Key Responsibilities:

    • Lead & Execute: Support routine cGMP testing for raw materials and finished products, specializing in Cell-based assays and ELISA.
    • Innovate & Troubleshoot: Act as the SME for laboratory equipment and assay performance issues.
    • Quality Ownership: Manage quality records, including Investigations, CAPAs, and Change Controls.
    • Mentor: Teach and train junior analysts on technical concepts and aseptic techniques.
    • Collaborate: Partner with Manufacturing, QA, and Development groups to facilitate seamless method transfers.

    What You'll Need to Succeed

    • Education: BA/BS in a STEM field.
    • Experience: Minimum 5 years in a cGMP laboratory environment.
    • Technical Mastery: Hands-on experience with Mammalian cells, Cell-based Assays, ELISA, and Protein Analysis (IVRP).
    • The "Specialist" Edge: Proven experience in method validation/qualification and technical writing (SOPs/Protocols).
    • Operational Excellence: Aseptic technique proficiency and a deep understanding of FDA, EU, and ICH guidelines.
    • Mindset: Ability to thrive in a fast-paced, matrixed environment with a focus on "Right First Time" execution.

    Quick Specs

    • Location: Norwood, MA (100% On-site)
    • Shift: Monday – Friday, 2nd Shift (12:00 PM – 8:00 PM)
    • Pay: $41.00/hour + 10% Shift Differential
    • Duration: 6-Month Contract (Potential for extension/conversion)
    • Target Start: March 16, 2026

    Note: Candidates must currently hold U.S. work authorization as immigration sponsorship is not available for this role.

    Ready to lead the way in QC? APPLY NOW

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