Process Operator
GSK
4 hours ago
On-site
Zebulon, NC
Operations
Process Operator
As a Process Operator you will operate, challenge and clean equipment per SOPs, JSAs, and batch documents to manufacture high quality products safely. You will monitor equipment for excessive rejects, resolve minor downtime, and identify improvement opportunities. You will perform changeovers and set up equipment to design specifications while meeting regulatory and OSHA requirements.
Key Responsibilities:
- Operate, challenge, replenish consumables, clean equipment; maintain inspection readiness with minimal supervision (cGMP, batch documentation, SOPs, ZSPs, JSAs).
- Monitor for excessive rejects/stoppages and use performance data to escalate quality/safety/line performance issues.
- Participate in GSK Production System standards (5S, standard work, problem solving, Gemba, process confirmations, performance management) toward Zero Accidents/Defects/Waste.
- Support performance management entry and problem-solving steps 1–3; perform/maintain OSW and 5S.
- Troubleshoot and resolve minor equipment stoppages; improve safety, quality, waste & performance.
- Use required systems/applications (e.g., DELTA, my Learning, Free Weigh, DISY, Active Plant, IP21, SAP basic transactions).
- Perform equipment changeovers and start-of-batch activities to designed specifications; certify on multiple technologies.
Basic Qualifications:
- High School Diploma or GED
- 1+ years pharma/manufacturing experience
- Ability to handle up to 40 lbs.
- Ability to work up to 12.5 hours in one shift (if required)
Preferred Qualifications (plus):
- Data accuracy/analysis; mechanical aptitude; OEE knowledge; data entry/computer & HMI competence; familiarity with relevant applications.
Physical/Other:
- Ability to work in manufacturing environment; follow written/verbal instructions; use PPE; work overtime as needed; perform required physical tasks.
As a Process Operator you will operate, challenge and clean equipment per SOPs, JSAs, and batch documents to manufacture high quality products safely. You will monitor equipment for excessive rejects, resolve minor downtime, and identify improvement opportunities. You will perform changeovers and set up equipment to design specifications while meeting regulatory and OSHA requirements.
Key Responsibilities:
- Operate, challenge, replenish consumables, clean equipment; maintain inspection readiness with minimal supervision (cGMP, batch documentation, SOPs, ZSPs, JSAs).
- Monitor for excessive rejects/stoppages and use performance data to escalate quality/safety/line performance issues.
- Participate in GSK Production System standards (5S, standard work, problem solving, Gemba, process confirmations, performance management) toward Zero Accidents/Defects/Waste.
- Support performance management entry and problem-solving steps 1–3; perform/maintain OSW and 5S.
- Troubleshoot and resolve minor equipment stoppages; improve safety, quality, waste & performance.
- Use required systems/applications (e.g., DELTA, my Learning, Free Weigh, DISY, Active Plant, IP21, SAP basic transactions).
- Perform equipment changeovers and start-of-batch activities to designed specifications; certify on multiple technologies.
Basic Qualifications:
- High School Diploma or GED
- 1+ years pharma/manufacturing experience
- Ability to handle up to 40 lbs.
- Ability to work up to 12.5 hours in one shift (if required)
Preferred Qualifications (plus):
- Data accuracy/analysis; mechanical aptitude; OEE knowledge; data entry/computer & HMI competence; familiarity with relevant applications.
Physical/Other:
- Ability to work in manufacturing environment; follow written/verbal instructions; use PPE; work overtime as needed; perform required physical tasks.