Lead QC Analytical Supervisor: Testing & Compliance

PCI Pharma Services; Bedford (NH); On-site; USD 90,000 - 120,000; Full time

Job summary

PCI Pharma Services is seeking a QC Analytical Supervisor in New Hampshire to lead the analytical lab, perform peer reviews, and ensure CGMP-compliant testing of in-process, quality control, and finished product samples. You will oversee method validation, SOP updates, and investigations into OOS events, while coordinating with QA and client communications.

The role requires 5+ years in analytical chemistry within pharma QC, CGMP proficiency, and prior leadership experience. Travel is <10%, and strong documentation skills are essential.

Qualifications

• 5+ years of Analytical Chemistry experience in pharmaceutical QC
• Experience working in a cGMP laboratory
• Experience working in a CMO environment preferred
• Bachelor of Science in a scientific area
• Master of Science in a scientific area and 3+ years Analytical Chemistry experience

Responsibilities

• Prioritize and distribute work to analysts in the QC Analytical laboratory
• Conduct OOS and customer complaint investigations
• Complete peer review of work in the analytical laboratory
• Train new employees
• Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing
• Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation
• Perform instrument calibrations and preventative maintenance
• Document laboratory work meeting CGMP requirements
• Write, review and revise SOPs as required
• Other duties as assigned or required

Skills

Analytical chemistry

Leadership

Communication

Multi-tasking

Teamwork

Integrity

Education

Bachelor of Science in a scientific area

Master of Science in a scientific area with 3+ years experience

Tools

HPLC

Karl Fischer

UV Vis

Densitometer

Osmometer

Job description

PCI Pharma Services is seeking a QC Analytical Supervisor in New Hampshire to lead the analytical lab, perform peer reviews, and ensure CGMP-compliant testing of in-process, quality control, and finished product samples. You will oversee method validation, SOP updates, and investigations into OOS events, while coordinating with QA and client communications.

The role requires 5+ years in analytical chemistry within pharma QC, CGMP proficiency, and prior leadership experience. Travel is <10%, and strong documentation skills are essential.