GMP QC Supervisor — Lead Analytical & Micro Lab

Piramal Pharma Limited; Sellersville (Bucks County); On-site; GBP 67,000 - 89,000; Full time

Job summary

Piramal Pharma Solutions is seeking an experienced QC Supervisor to lead a team of 4–5 analysts at the Sellersville, PA facility. The role involves supervising laboratory operations, ensuring GMP compliance, and driving operational excellence within Quality Control.

You will review data from HPLC, UPLC, GC, and ICP-MS and coordinate testing with production. Responsibilities include OOS/OOT investigations, CAPAs, change controls, and regulatory readiness support, with a focus on data integrity

Qualifications

• Bachelor's degree in a scientific discipline (Chemistry, Biology, Microbiology, Pharmaceutical Sciences)
• 7+ years of technical laboratory experience in a GMP-regulated environment
• 5+ years of leadership or supervisory experience
• Experience with analytical chemistry and/or microbiological testing
• Hands-on experience with HPLC, UPLC, and GC instrumentation
• Knowledge of GMP, FDA, ICH, and USP requirements
• Experience with Empower, LIMS, and TrackWise preferred

Responsibilities

• Supervise daily activities of 4–5 QC analysts.
• Plan, coordinate, and prioritize laboratory testing to support manufacturing schedules.
• Review analytical data from HPLC, UPLC, GC, and ICP-MS.
• Ensure testing per SOPs, USP, EP and regulatory requirements.
• Coordinate sampling and testing for production operations.
• Lead investigations (OOS/OOT), CAPAs, and change controls.
• Maintain and review SOPs; prepare training and performance guidance.
• Support regulatory readiness and site quality initiatives.

Skills

Leadership

Team Development

Analytical Chemistry

Communication

Data Integrity

Multitasking

Education

Bachelor's degree in Chemistry or related

Tools

HPLC

UPLC

GC

ICP-MS

Empower

LIMS

TrackWise

Job description

Piramal Pharma Solutions is seeking an experienced QC Supervisor to lead a team of 4–5 analysts at the Sellersville, PA facility. The role involves supervising laboratory operations, ensuring GMP compliance, and driving operational excellence within Quality Control.

You will review data from HPLC, UPLC, GC, and ICP-MS and coordinate testing with production. Responsibilities include OOS/OOT investigations, CAPAs, change controls, and regulatory readiness support, with a focus on data integrity