Fall Co-op/Biopharmaceutical Manufacturing
About The Position
This six-month position (August 2026-January 2027) sits within the Manufacturing Specialist department. The department supports the direct manufacture of biopharmaceutical bulk drug substance intended for commercial and/or clinical use. The Production organization is comprised of manufacturing associates, supervisors, managers, and manufacturing specialists who support all Production activities. The Manufacturing Specialist Co-Op will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) daily by engaging positively with team members and production support groups. This position is responsible for performing an array of tasks ranging from management of GMP documentation, management of inventory of raw materials and single-use components in the manufacturing areas, ownership of continuous improvement initiatives, participation in manufacturing investigations, among other key activities.
Requirements
- Pursuing a degree in natural science or engineering discipline.
- Must be able to work full-time (35-40 hours/week) throughout the duration of the 6 month co-op (August 2026 ~ January 2027).
- Must have an active student status and/or within 12 months post-graduation from a BS or MS degree program.
- Post-doctoral candidates are not eligible.
- Must successfully pass a drug screen and background check prior to assignment target start date.
Nice To Haves
- Students actively enrolled in an undergraduate degree program are strongly preferred.
- Technically oriented candidate with prior experience with biopharmaceutical operations via coursework, lab work, or industrial experience is highly preferred.
- Ideal candidate will exhibit strong interpersonal skills and take initiative to learn and engage with process subject matter experts (SMEs).
- Candidate should demonstrate the ability to follow current Good Manufacturing Practices (cGMP) and work in a highly regulated environment.
Responsibilities
- Management of GMP documentation
- Management of inventory of raw materials and single-use components in the manufacturing areas
- Ownership of continuous improvement initiatives
- Participation in manufacturing investigations
Benefits
- Competitive hourly pay rate
- Relocation stipend for candidates hired for an on-site or hybrid role who reside outside of 50-miles from their assigned work location.
- Medical benefits
- Fringe benefits
- Employee Assistance Program
- Overtime pay
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
Associate degree
