Winter Co-op/Biopharmaceutical Manufacturing
About The Position
This six-month co-op, running January through June 2027, is within GSK’s Production Specialist department, which supports the manufacture of biopharmaceutical bulk drug substance for commercial and/or clinical use. The Manufacturing Specialist Co-Op joins a high-performing team responsible for supplying GSK products to the One Biopharm supply chain. The role involves managing GMP documentation and manufacturing-area inventories of raw materials and single-use components, owning continuous-improvement initiatives, and participating in manufacturing investigations. The co-op is expected to demonstrate GSK’s values of Patient Focus, Transparency, Respect, and Integrity, and its expectations of Courage, Accountability, Development, and Teamwork through positive engagement with colleagues and production support groups. This is a temporary position as an employee of Atrium on assignment at GSK. It requires full-time availability of 35–40 hours per week for the full six-month period. The role is onsite or hybrid depending on the position details; the posting does not specify which applies to this role. The position is eligible for overtime pay. The stated pay rate range is $22 to $43 per hour.
Requirements
- Be pursuing a degree in a natural science or engineering discipline.
- Be able to work full-time, 35–40 hours per week, throughout the six-month co-op from January through June 2027.
- Have active student status and/or be within 12 months post-graduation from a BS or MS degree program; post-doctoral candidates are not eligible.
- Successfully pass a drug screen and background check before the target assignment start date.
- Complete the GSK Digital Assessment and achieve a passing score to proceed in the application process.
Nice To Haves
- Prior biopharmaceutical operations experience through coursework, laboratory work, or industrial experience.
- Strong interpersonal skills and initiative to learn from and engage with process subject matter experts.
- Ability to follow current Good Manufacturing Practices (cGMP) and work in a highly regulated environment.
Responsibilities
- Support the manufacture of biopharmaceutical bulk drug substance for commercial and/or clinical use.
- Help deliver GSK product supply to the One Biopharm supply chain.
- Manage GMP documentation.
- Manage inventories of raw materials and single-use components in manufacturing areas.
- Own continuous-improvement initiatives.
- Participate in manufacturing investigations.
- Engage positively with team members and production support groups while demonstrating GSK values and expectations.
Benefits
- Competitive hourly pay rate and benefits; benefits eligibility is determined the month following the date of hire.
- A one-time relocation stipend may be available to eligible candidates hired for an onsite or hybrid role who reside more than 50 miles from the assigned work location.
- Overtime pay in accordance with federal and state requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
