QC Manager - Biologics

About the role

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. This is a permanent position.

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. Bachelor’s degree required.

Skills

Quality Control (QC)

Benefits

• Medical insurance
• Prescription coverage
• Dental insurance
• Vision insurance
• AD&D insurance
• Life insurance
• Short-term disability
• 401(k) plan

Pay

$120,000 - $140,000 per year

Schedule

9:00 AM – 5:00 PM (onsite)