Process Operator
Listed on 2026-06-27
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Manufacturing / Production
Production Associate / Production Line, Manufacturing Production, Production QC/QA
Business Introduction
We manufacture and supply reliable, high‑quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 manufacturing sites delivered 1.7billion packs of medicines and 409million vaccine doses in 2024.
Position SummaryYou will operate, clean and maintain production equipment following standard operating procedures, safety rules and batch documentation. Monitor equipment performance and product quality, report or escalated issues that affect safety or output, and perform routine changeovers and start‑of‑batch activities to meet production specifications. Complete required production records and basic system entries accurately and on time. Support continuous improvement by suggesting practical fixes and participating in basic problem solving.
Responsibilities- Operate and maintain manufacturing equipment to deliver high‑quality products safely and reliably.
- Follow standard procedures and batch documentation while working closely with technicians and supervisors.
- Perform routine changeovers, start‑of‑batch activities, and operational checks in accordance with specifications.
- Monitor equipment performance and product quality, and report or escalated issues that affect safety or output.
- Support continuous improvement by suggesting practical fixes and participating in basic problem‑solving.
- Work with teammates and supervisors to troubleshoot minor production stoppages and hand off technical issues as needed.
- Maintain consumable supplies, clean equipment, and complete all required duties for smooth production.
- Schedule and maintain inspection readiness and follow technical documentation.
- High school diploma or GED.
- 1+ year of manufacturing or production experience.
- Ability to lift and handle materials up to 40pounds.
- Basic reading, writing, and math skills.
- Comfort using computers for basic data entry and training systems.
- Experience in regulated manufacturing environments.
- Willingness to work site‑based, including shift patterns and up to 12.5‑hour shifts when required.
- Experience with equipment set‑up, changeovers, and routine operational checks.
- Basic mechanical aptitude and ability to read gauges and instrumentation.
- Familiarity with human machine interfaces (HMI) or production data systems.
- Experience following technical documentation and maintaining inspection readiness.
- Exposure to continuous improvement tools such as 5S or standard work.
This role is on‑site in the United States. Hybrid or remote work is not available. Shift patterns will match site operational needs.
What you can expectJoin a team that values inclusion, safety and learning. Training and mentoring are available to help you develop new skills. If you enjoy hands‑on work, solving practical problems, and growing your technical know‑how, we would like to hear from you. We look forward to hearing from you.
Equal Opportunity EmployerGSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited by federal, state or local law.
Accommodation RequestIf you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at usre
Employment Agency NoticeGSK does not accept referrals from employment businesses and/or employment agencies for the vacancy posted on this site. All employment businesses/agencies are required to obtain prior written authorization from GSK’s procurement/human resources department before referring any candidates. Any actions undertaken by the employment business/agency without such authorization are deemed performed without the consent or contractual agreement of GSK.
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