QC Supervisor - Lead Analytical Lab and GMP Excellence

Piramal Pharma Limited; Northern (KY); Hybrid; USD 70,000 - 110,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Quality Control Supervisor to lead a team of QC analysts at the Sellersville, PA site. The role focuses on supervising lab operations, ensuring GMP compliance, and driving continuous improvement in analytical testing across raw materials, intermediates, and finished products.

The incumbent will review data from HPLC, UPLC, GC, and ICP-MS, manage CAPAs and deviations, and support regulatory readiness and system administrations (Empower, LIMS, TrackWise).

Qualifications

• Bachelor's degree in Chemistry, Biology, Microbiology, or pharmaceutical sciences.
• 7+ years of technical lab experience in a GMP environment.
• 5+ years of leadership or supervisory experience.
• Experience with analytical chemistry and microbiological testing.

Responsibilities

• Supervise daily activities of approximately 4–5 QC analysts.
• Plan, coordinate, and prioritize lab testing to support manufacturing and supply chain.
• Review analytical data from HPLC, UPLC, GC, and ICP-MS.
• Ensure testing complies with SOPs, USP, EP and regulatory requirements.
• Coordinate sampling and testing for production operations.
• Lead cleaning validation and verification testing programs.
• Support regulatory compliance initiatives and site quality goals.
• Provide training and coaching to QC staff.

Skills

Leadership

Analytical chemistry

GMP compliance

Data integrity

Laboratory supervision

Education

Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences

Tools

HPLC

UPLC

GC

ICP-MS

LIMS

TrackWise

Job description

Piramal Pharma Solutions is seeking a Quality Control Supervisor to lead a team of QC analysts at the Sellersville, PA site. The role focuses on supervising lab operations, ensuring GMP compliance, and driving continuous improvement in analytical testing across raw materials, intermediates, and finished products.

The incumbent will review data from HPLC, UPLC, GC, and ICP-MS, manage CAPAs and deviations, and support regulatory readiness and system administrations (Empower, LIMS, TrackWise).