Biopharmaceutical Manufacturing Associate II
GSK
14 hours ago
On-site
King of Prussia, PA
Operations
Responsibilities:
- Perform biopharm production operations including fermentation/cell culture, solution preparation, chromatographic separation, filtration and concentration, autoclave/parts washing, and area cleaning/upkeep.
- Complete daily manufacturing tasks and increase competency across production areas over time.
- Participate in safety and compliance initiatives and investigations; help solve technical/organizational problems.
- Engage with the GSK Production System to continuously improve safety, quality, and schedule/cost performance.
- Complete and document manufacturing tasks safely and compliantly using SOPs, batch instructions, and logbooks (data integrity).
- Proactively work with senior staff to build production operation competency.
- Support cross-functional activities (engineering, validation, tech transfer), including safety/compliance input; may require off-site work (e.g., FAT support).
- Monitor equipment and critical process parameters; escalate abnormalities and participate in troubleshooting.
- Maintain competency with digital platforms (e.g., SAP, EBR, AR/VR) and ensure equipment/material availability by daily schedule review.
- Participate transparently in safety/compliance-driven investigations.
Qualifications:
- BS/BA degree with cGMP manufacturing experience.
- OR Associate’s degree (Biotechnology or related) with cGMP manufacturing experience.
- OR High school diploma with 1+ year of cGMP manufacturing experience.
Preferred Qualifications:
- Demonstrated high performance.
- Strong verbal and written skills.
- Ability to work well in a team environment.
- Ability to follow detailed processing instructions and accurately document required records.
- Perform biopharm production operations including fermentation/cell culture, solution preparation, chromatographic separation, filtration and concentration, autoclave/parts washing, and area cleaning/upkeep.
- Complete daily manufacturing tasks and increase competency across production areas over time.
- Participate in safety and compliance initiatives and investigations; help solve technical/organizational problems.
- Engage with the GSK Production System to continuously improve safety, quality, and schedule/cost performance.
- Complete and document manufacturing tasks safely and compliantly using SOPs, batch instructions, and logbooks (data integrity).
- Proactively work with senior staff to build production operation competency.
- Support cross-functional activities (engineering, validation, tech transfer), including safety/compliance input; may require off-site work (e.g., FAT support).
- Monitor equipment and critical process parameters; escalate abnormalities and participate in troubleshooting.
- Maintain competency with digital platforms (e.g., SAP, EBR, AR/VR) and ensure equipment/material availability by daily schedule review.
- Participate transparently in safety/compliance-driven investigations.
Qualifications:
- BS/BA degree with cGMP manufacturing experience.
- OR Associate’s degree (Biotechnology or related) with cGMP manufacturing experience.
- OR High school diploma with 1+ year of cGMP manufacturing experience.
Preferred Qualifications:
- Demonstrated high performance.
- Strong verbal and written skills.
- Ability to work well in a team environment.
- Ability to follow detailed processing instructions and accurately document required records.