QC Biochemistry Manager

GSK•Marietta, PA

16h•Onsite

About The Position

You will lead and grow a quality control biochemistry team that ensures safe and compliant laboratory testing. You will work closely with production, quality assurance, and cross-functional partners. We value clear thinkers who coach others, drive continuous improvement, and focus on reliable results. This role offers career growth, the chance to shape lab strategy, and meaningful impact aligned with our mission: uniting science, technology and talent to get ahead of disease together.

Requirements

Bachelor’s degree in biochemistry, chemistry, molecular biology or related scientific discipline.
Minimum 5 years' experience in a GMP-regulated analytical laboratory environment.
Minimum 3 years' experience in a supervisory or manager role overseeing laboratory personnel.
Hands-on experience with biochemical or analytical techniques such as chromatography, electrophoresis, protein assays, or similar methods.
Demonstrated experience with method validation, method transfer, and laboratory investigations.
Strong record of managing laboratory documentation and supporting audits or inspections.

Nice To Haves

Master’s degree in a relevant scientific field.
Experience in biopharmaceutical or biologics testing environments.
Experience leading continuous improvement initiatives such as lean or Six Sigma projects.
Familiarity with stability study design and sample management practices.
Strong stakeholder management and cross-functional collaboration skills.
Experience managing laboratory budgets, equipment qualification, and lifecycle activities.

Responsibilities

Lead day-to-day QC biochemistry operations to meet testing timelines for product release, raw material, in-process and stability samples.
Develop and coach a team of analysts and supervisors to build capability and deliver consistent, high-quality results.
Oversee method transfers, validations, and troubleshooting for analytical assays used in release and stability testing.
Maintain compliance with good manufacturing practices and regulatory expectations through strong documentation and audit readiness.
Drive continuous improvement projects to enhance lab efficiency, quality and equipment uptime.
Manage resources including budgets, equipment lifecycle, and sample inventory to support reliable laboratory capacity.