Manufacturing Technician II (3rd Shift)
GSK
July 02, 2026
On-site
Marietta, PA
Operations
Position Summary
- Lead and execute complex vaccine drug substance manufacturing operations; serve as a technical expert providing on-floor leadership, training, problem-solving, and continuous improvement. Partner with supervision and cross-functional teams for compliant, safe, and efficient production.
Responsibilities
- Execute drug substance manufacturing (reagent/buffer prep: weighing, formulation, pH adjustment/titration, filtration, aliquoting) per approved batch records/SOPs.
- Operate/monitor automated equipment (chromatography, filtration systems, mixers, pumps, meters, scales) for safe, compliant execution.
- Use digital systems (electronic batch records, SCADA) to ensure data integrity, monitor trends, identify deviations, and improve outcomes.
- Adhere to GMP cleanroom requirements; perform/coordinate environmental monitoring, cleaning, and sanitization.
- Troubleshoot equipment, respond to alarms, escalate abnormalities; document status and contribute to reliability/asset-lifecycle initiatives.
- Maintain accurate contemporaneous GMP documentation; participate in SOP authoring/revision; recognize/report deviations; support investigations/RCA/CAPA.
- Develop/deliver training; support onboarding/qualification; lead activities in supervisor absence.
- Participate in troubleshooting and continuous improvement (5S/problem solving).
Qualifications
Required:
- Bachelor’s in biological sciences/chemistry/engineering or related field; equivalent education/experience acceptable (incl. 3+ years relevant GMP experience or certifications).
- 1+ year manufacturing/production experience.
- Leadership experience in GMP manufacturing.
- Technical writing experience for GMP documentation (SOPs/MBRs/training) with GMP knowledge.
Preferred:
- BS/BA in biological/chemical science; experience authoring regulated technical docs.
- On-floor GMP technical leadership; chemical handling with PPE.
- Ability to perform math and accurate measurements.
- Digital agility (SAP/SCADA/MES/Microsoft Office); cleanroom operations experience.
- Lift up to 40 lbs; strong verbal/written communication; digital and automated tools experience.
Work Arrangement
- On-site in the United States; multiple shifts; 3rd shift eligible for 15% shift differential. Possible noise/moving parts; required PPE; standing/walking and physical tasks; overtime may be required.
Application Instructions
- Apply now; submit your resume and a short note on what you’ll bring to the team.
- Lead and execute complex vaccine drug substance manufacturing operations; serve as a technical expert providing on-floor leadership, training, problem-solving, and continuous improvement. Partner with supervision and cross-functional teams for compliant, safe, and efficient production.
Responsibilities
- Execute drug substance manufacturing (reagent/buffer prep: weighing, formulation, pH adjustment/titration, filtration, aliquoting) per approved batch records/SOPs.
- Operate/monitor automated equipment (chromatography, filtration systems, mixers, pumps, meters, scales) for safe, compliant execution.
- Use digital systems (electronic batch records, SCADA) to ensure data integrity, monitor trends, identify deviations, and improve outcomes.
- Adhere to GMP cleanroom requirements; perform/coordinate environmental monitoring, cleaning, and sanitization.
- Troubleshoot equipment, respond to alarms, escalate abnormalities; document status and contribute to reliability/asset-lifecycle initiatives.
- Maintain accurate contemporaneous GMP documentation; participate in SOP authoring/revision; recognize/report deviations; support investigations/RCA/CAPA.
- Develop/deliver training; support onboarding/qualification; lead activities in supervisor absence.
- Participate in troubleshooting and continuous improvement (5S/problem solving).
Qualifications
Required:
- Bachelor’s in biological sciences/chemistry/engineering or related field; equivalent education/experience acceptable (incl. 3+ years relevant GMP experience or certifications).
- 1+ year manufacturing/production experience.
- Leadership experience in GMP manufacturing.
- Technical writing experience for GMP documentation (SOPs/MBRs/training) with GMP knowledge.
Preferred:
- BS/BA in biological/chemical science; experience authoring regulated technical docs.
- On-floor GMP technical leadership; chemical handling with PPE.
- Ability to perform math and accurate measurements.
- Digital agility (SAP/SCADA/MES/Microsoft Office); cleanroom operations experience.
- Lift up to 40 lbs; strong verbal/written communication; digital and automated tools experience.
Work Arrangement
- On-site in the United States; multiple shifts; 3rd shift eligible for 15% shift differential. Possible noise/moving parts; required PPE; standing/walking and physical tasks; overtime may be required.
Application Instructions
- Apply now; submit your resume and a short note on what you’ll bring to the team.