Position Summary
We are recruiting several positions in the Vials and Syringe business unit. Applicants will be considered for one of the following roles: Vials Inspect & Packaging Operators, Syringe Inspect, Assemble & Packaging Operators, Enhanced Operators, Vials Process Operators. You will work at the Barnard Castle Manufacturing site in the Steriles Packaging & Inspection or Grade C filling area, collaborating with Production, Quality, Engineering, MSAT and Warehouse teams.
Key Responsibilities
- Complete batch documentation and production equipment logs accurately and timely per procedures and GMP standards.
- Set up and operate semi‑automatic and fully automatic packaging, assembly and inspection machines, ensuring efficient production and performing critical device and guard check challenges.
- Work in a classified production area filling terminally sterilised products.
- Stage, retrieve and transfer components, containers and finished packs to support packaging lines.
- Inspect finished packs for quality, perform visual inspections, and record findings accurately.
- Prepare, check and reconcile batch documentation, labels and records to maintain traceability.
- Report and escalates production, quality or stock discrepancies, working with the team to resolve issues through problem solving.
Basic Qualifications
- Experience working in a production packaging, inspection or filling environment.
- Ability to read and follow written procedures and complete accurate records.
- Good attention to detail when inspecting products and preparing documentation.
- Comfortable working on‑site in controlled environments.
- Flexibility and willingness to work shift patterns required to meet changing production schedules.
- Team player with clear verbal communication and a willingness to learn and develop.
Preferred Qualifications
- Experience in regulated manufacturing or healthcare production environments.
- Practical experience with digital production systems such as SAP & EBRS.
- Experience handling temperature‑controlled or cold‑chain materials.
- Familiarity with Good Manufacturing Practice (GMP) principles.
- Experience contributing to continuous improvement activities and problem solving.
Working Arrangement
This position is on‑site at our United Kingdom manufacturing facility. Shift work is required to meet production needs. Specific shift patterns and hours will be discussed during the hiring process.
Equal Opportunity Employer
GSK is an Equal Opportunity Employer. We ensure that all qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law.
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