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QC Manager - Biologics

Job in Fort Lauderdale, Broward County, Florida, 33336, USA
Listing for: Randstad USA
Full Time position
Listed on 2026-10-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, Data Analyst
Salary/Wage Range or Industry Benchmark: 120000 USD Yearly USD 120000.00 YEAR
Job Description & How to Apply Below
Job Summary

Are you a high-performing QC Supervisor ready to step into a pivotal leadership role with a premier Biologics CDMO in sunny Ft. Lauderdale, FL? We are seeking a Quality Control Manager to lead analytical testing operations in a dynamic, fast-paced environment. In this onsite role, you will drive analytical excellence, direct method transfers, and empower a high-impact team developing cutting-edge biotherapeutics.

Job Summary

Are you a high-performing QC Supervisor ready to step into a pivotal leadership role with a premier Biologics CDMO in sunny Ft. Lauderdale, FL? We are seeking a Quality Control Manager to lead analytical testing operations in a dynamic, fast-paced environment. In this onsite role, you will drive analytical excellence, direct method transfers, and empower a high-impact team developing cutting-edge biotherapeutics.

location:
Fort Lauderdale, Florida

job type:
Permanent

salary: $120, per year

work hours: 9 to 5

education:
Bachelors

skills:
Quality Control (QC)

Responsibilities
  • Lead, mentor, and develop a team of QC Analysts and Scientists performing analytical testing for biologics, vaccines, and cell/gene therapies.
  • Provide technical oversight for analytical methods including HPLC/UPLC, bioassays, plate-based assays, CE, qPCR, and spectroscopy.
  • Lead OOS, OOT, and atypical investigations, executing root cause analysis and robust CAPAs to ensure GMP compliance.
  • Serve as the QC Analytical Subject Matter Expert during regulatory inspections, client meetings, and audits.
  • Collaborate cross-functionally with QA, Manufacturing, and Tech Ops to optimize laboratory performance and data integrity.
Qualifications
  • Minimum of 5-7 years of progressively responsible experience in Quality Control, within an FDA-regulated CDMO or biopharmaceutical environment supporting high-volume New Product Introductions (NPIs).
  • Proven experience managing multi-product portfolios across 8-10+ distinct assays.

Equal Opportunity

Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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