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Quality Control Associate II, Microbiology

Quality Control Associate II, Microbiology

RandstadNorwood, MA, US
2 days ago
Job type
  • Temporary
Job description

Job Description

Job Description

Quality Control Associate II (Microbiology | cGMP Lab)

Location : Norwood, MA 02062 (Onsite – Not Remote)

Schedule : Monday–Friday, 9 : 00 AM–5 : 00 PM

Duration : 6-Month Contract | Target Dates : December 4, 2025 – June 5, 2026

Pay Rate : $50.00 per hour

About the Role

We’re seeking an experienced and detail-oriented Quality Control Associate II to support cGMP QC microbiology testing and quality systems activities at our state-of-the-art manufacturing site in Norwood, MA .

In this role, you’ll perform routine QC testing for raw materials, drug substances, and finished products, while ensuring compliance with Good Manufacturing Practices (cGMP) and internal quality standards. You’ll work hands-on in a dynamic, fast-paced environment, collaborating with cross-functional teams to uphold quality and operational excellence.

Key Responsibilities

  • Perform QC microbiology testing, including bioburden, endotoxin, sterility, TOC, and microbial enumeration .
  • Maintain, calibrate, and troubleshoot laboratory equipment.
  • Manage QC laboratory supplies and inventory.
  • Author, review, and revise SOPs, protocols, and technical reports .
  • Participate in deviations, CAPAs, change controls, and non-conformance investigations .
  • Support audit readiness and continuous improvement initiatives.
  • Ensure strict adherence to cGMP documentation practices and regulatory requirements .
  • Maintain a clean, organized, and safe laboratory environment.

Qualifications

Education : Bachelor’s degree in a STEM discipline (Biology, Microbiology, Chemistry, or related field).

Experience : 2–3 years of hands-on experience in a cGMP laboratory , preferably in microbiology or biopharma QC .

Preferred Skills & Competencies :

  • Proficiency in Microsoft Office and electronic systems (LIMS, SAP, eQMS).
  • Strong understanding of GMP, aseptic technique, and laboratory instrumentation .
  • Knowledge of FDA, EU, and ICH regulatory guidelines.
  • Excellent troubleshooting, organization, and communication skills.
  • Ability to manage multiple projects in a fast-paced, collaborative environment.

    • Why Join

  • Opportunity to work in a cutting-edge biotech environment supporting life-changing therapeutics.
  • Exposure to advanced QC systems and global quality standards.
  • Be part of a passionate, mission-driven team committed to scientific excellence and patient impact.

    • ✅ Ready to take the next step in your quality control career?

    Apply now to join a world-class organization where your skills will directly contribute to improving global health.

    FOR MORE IMMEDIATE CONSIDERATION, email a current resume to iris.levy@randstadusa.com

    Company Description

    Randstad Staffing. We provide outsourcing, staffing, consulting, and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration, and sales and marketing.

    We can’t wait to tell you all about it!

    Company Description

    Randstad Staffing. We provide outsourcing, staffing, consulting, and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration, and sales and marketing. \r\n\r\nWe can’t wait to tell you all about it!

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    Quality Associate Ii • Norwood, MA, US