QC Supervisor – GMP Lab Leader

Cambrex Corp.; Charles City (IA); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Healthcare

Life insurance

Retirement planning

Job summary

Cambrex is a leading global CDMO that provides drug substance development and manufacturing across the drug lifecycle. The QC Supervisor will provide supervisory oversight, laboratory testing support, and technical leadership for laboratory staff.

Responsibilities include coordinating daily QC testing, maintaining instruments, ensuring cGMP compliance, and overseeing offsite sample testing and documentation.

Qualifications

• Familiarity with cGMP, safety and regulatory environments.
• Operational knowledge of HPLC/UPLC, GC, IC, ICP, FTIR, UV‑VIS.
• Computer literacy with word processing, spreadsheets, databases.

Responsibilities

• Coordinate daily prioritization of QC testing and staff/equipment use.
• Maintain instrumentation, qualification, and preventive maintenance.
• Support training and troubleshooting for staff.
• Review data and facilitate timely release of results.

Skills

cGMP familiarity

Analytical instrumentation

Data management (Windows)

Chemistry knowledge

Education

Bachelor's Degree in Chemistry/Pharmacy or related field

Advanced degree beneficial

Job description

Cambrex is a leading global CDMO that provides drug substance development and manufacturing across the drug lifecycle. The QC Supervisor will provide supervisory oversight, laboratory testing support, and technical leadership for laboratory staff.

Responsibilities include coordinating daily QC testing, maintaining instruments, ensuring cGMP compliance, and overseeing offsite sample testing and documentation.