Randstad USA
Quality Control Associate II (Microbiology | cGMP Lab)
Duration: 6-Month Contract | Target Dates: December 4, 2025 – June 5, 2026
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 .
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
Seniority: Associate | Employment type: Contract | Job function: Quality Assurance and Science | Industries: Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
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 .
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
Seniority: Associate | Employment type: Contract | Job function: Quality Assurance and Science | Industries: Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr