Biomanufacturing Associate III
GSK
July 01, 2026
On-site
King of Prussia, PA
Operations
Position Summary:
You will work as a Biomanufacturing Associate III in a manufacturing team that delivers safe, high-quality medicines to patients. You will lead complex production activities, support troubleshooting and mentor colleagues.
Responsibilities:
- Lead and perform complex production tasks following SOPs and batch documentation.
- Manage equipment changeovers and start-of-batch activities with accurate, contemporaneous documentation.
- Monitor process parameters and product quality; escalate issues and drive root cause resolution.
- Coach and train colleagues on standard work, safety practices and operational procedures.
- Use production systems and basic data tools to record performance, identify trends and support continuous improvement.
- Support commissioning, validation and engineering activities during production transitions.
- Notify appropriate personnel of incidents/accidents; report abnormalities or adverse events to FLL (OLN, Rapid Response, deviation) in a timely manner; perform area cleaning and record per procedure.
Basic Qualifications (Required):
- 2+ years’ experience in a regulated manufacturing environment (or equivalent).
- 1+ year of experience in Sterile or GMP Cleaning operations in Pharmaceutical/Biotechnology (or 5+ years equivalent).
- High school diploma or GED (or equivalent practical experience).
- Demonstrated experience performing equipment changeovers and start-of-batch activities.
- Proven experience completing accurate batch documentation and following SOPs.
Preferred Qualifications:
- Associate degree/technical certificate (or equivalent) in a relevant field.
- Experience in pharmaceutical/biotech/regulated manufacturing.
- Mechanical aptitude; ability to read gauges and instrumentation.
- Experience using production systems/electronic batch records or SAP.
- Experience coaching/training colleagues and contributing to written work instructions.
- Exposure to continuous improvement methods (5S, standard work, basic problem solving).
Workplace Expectations:
- On-site in the United States; shift work in a regulated manufacturing environment (may include 12-hour shifts and day/night rotations).
- Noise/moving equipment; wear required PPE; follow cleanroom rules when applicable.
- Lift up to 40 lbs.; kneeling, climbing, standing; willingness to work extended shift lengths.
Application Instructions:
- Apply and tell us about times you led production activities, coached colleagues, or solved process problems.
You will work as a Biomanufacturing Associate III in a manufacturing team that delivers safe, high-quality medicines to patients. You will lead complex production activities, support troubleshooting and mentor colleagues.
Responsibilities:
- Lead and perform complex production tasks following SOPs and batch documentation.
- Manage equipment changeovers and start-of-batch activities with accurate, contemporaneous documentation.
- Monitor process parameters and product quality; escalate issues and drive root cause resolution.
- Coach and train colleagues on standard work, safety practices and operational procedures.
- Use production systems and basic data tools to record performance, identify trends and support continuous improvement.
- Support commissioning, validation and engineering activities during production transitions.
- Notify appropriate personnel of incidents/accidents; report abnormalities or adverse events to FLL (OLN, Rapid Response, deviation) in a timely manner; perform area cleaning and record per procedure.
Basic Qualifications (Required):
- 2+ years’ experience in a regulated manufacturing environment (or equivalent).
- 1+ year of experience in Sterile or GMP Cleaning operations in Pharmaceutical/Biotechnology (or 5+ years equivalent).
- High school diploma or GED (or equivalent practical experience).
- Demonstrated experience performing equipment changeovers and start-of-batch activities.
- Proven experience completing accurate batch documentation and following SOPs.
Preferred Qualifications:
- Associate degree/technical certificate (or equivalent) in a relevant field.
- Experience in pharmaceutical/biotech/regulated manufacturing.
- Mechanical aptitude; ability to read gauges and instrumentation.
- Experience using production systems/electronic batch records or SAP.
- Experience coaching/training colleagues and contributing to written work instructions.
- Exposure to continuous improvement methods (5S, standard work, basic problem solving).
Workplace Expectations:
- On-site in the United States; shift work in a regulated manufacturing environment (may include 12-hour shifts and day/night rotations).
- Noise/moving equipment; wear required PPE; follow cleanroom rules when applicable.
- Lift up to 40 lbs.; kneeling, climbing, standing; willingness to work extended shift lengths.
Application Instructions:
- Apply and tell us about times you led production activities, coached colleagues, or solved process problems.