QC Chromatography Senior Scientist
GSK
September 04, 2026
Remote friendly (Marietta, PA)
United States
Operations
Position Summary
You will provide high level scientific expertise to the Chromatography team for separation technologies (Normal and Reverse Phase Chromatography with detectors including QDa, PDA, RI, MALS, CAD; Gel Capillary electrophoresis, etc.), design/implement robust experiments, analyze data, document methods/results/conclusions, drive projects to closure, and ensure safe execution and GMP/regulatory compliance.
Responsibilities
- Ensure lab compliance with EHS policies; support safety and internal/external audits.
- Serve as Lab Investigation/Change Control/CAPA Task Owner; lead implementation and ensure timely closure (Orange Belt certified).
- Process/evaluate complex chromatography data.
- Act as SME for chromatography methods (performance, acceptance criteria, troubleshooting, validation, compendial requirements).
- Backup SAP and LES Business Approver: define business requirements, review updates, approve system entries/changes; manage reagent supply chain and coordinate creation/qualification of new materials/reagents.
- Drive implementation of new/updated methods (transfers, corrective/continuous control, CAPA, compendial updates) with protocol adherence and documentation.
- Provide SAP/LES implementation/upgrades input (master data, test plans, workflows); serve as Empower SME.
- Troubleshoot equipment/assays; coordinate preventive maintenance and escalations.
- Lead training and maintain competency records; create/maintain training materials.
- Lead/maintain 5S practices.
Basic Qualifications
- Bachelor’s degree in chemistry/biochemistry/analytical chemistry or related.
- 5+ years high-throughput laboratory testing.
- 5+ years GMP/FDA regulated environment.
- 5+ years QC chromatography lab experience (preferably with Empower).
Preferred Qualifications
- MS; knowledge of GMP/NIH/FDA and regulatory requirements.
- Astra software familiarity (MALS analysis).
- Urgency, flexibility, accountability; strong chromatography expertise.
- Strong data analysis/trending; detail-oriented in complex matrices.
- Intermediate/advanced computer skills; strong customer service.
- Stay current with field/GSK standards; strong communication and analytical method understanding.
How to apply
Submit resume plus a short note describing a chromatography method transfer, validation, or investigation you led (challenge, approach, outcome).
You will provide high level scientific expertise to the Chromatography team for separation technologies (Normal and Reverse Phase Chromatography with detectors including QDa, PDA, RI, MALS, CAD; Gel Capillary electrophoresis, etc.), design/implement robust experiments, analyze data, document methods/results/conclusions, drive projects to closure, and ensure safe execution and GMP/regulatory compliance.
Responsibilities
- Ensure lab compliance with EHS policies; support safety and internal/external audits.
- Serve as Lab Investigation/Change Control/CAPA Task Owner; lead implementation and ensure timely closure (Orange Belt certified).
- Process/evaluate complex chromatography data.
- Act as SME for chromatography methods (performance, acceptance criteria, troubleshooting, validation, compendial requirements).
- Backup SAP and LES Business Approver: define business requirements, review updates, approve system entries/changes; manage reagent supply chain and coordinate creation/qualification of new materials/reagents.
- Drive implementation of new/updated methods (transfers, corrective/continuous control, CAPA, compendial updates) with protocol adherence and documentation.
- Provide SAP/LES implementation/upgrades input (master data, test plans, workflows); serve as Empower SME.
- Troubleshoot equipment/assays; coordinate preventive maintenance and escalations.
- Lead training and maintain competency records; create/maintain training materials.
- Lead/maintain 5S practices.
Basic Qualifications
- Bachelor’s degree in chemistry/biochemistry/analytical chemistry or related.
- 5+ years high-throughput laboratory testing.
- 5+ years GMP/FDA regulated environment.
- 5+ years QC chromatography lab experience (preferably with Empower).
Preferred Qualifications
- MS; knowledge of GMP/NIH/FDA and regulatory requirements.
- Astra software familiarity (MALS analysis).
- Urgency, flexibility, accountability; strong chromatography expertise.
- Strong data analysis/trending; detail-oriented in complex matrices.
- Intermediate/advanced computer skills; strong customer service.
- Stay current with field/GSK standards; strong communication and analytical method understanding.
How to apply
Submit resume plus a short note describing a chromatography method transfer, validation, or investigation you led (challenge, approach, outcome).