Senior Process Operator

GlaxoSmithKline; Zebulon (NC); On-site; USD 40,000 - 55,000; Full time

Job summary

GlaxoSmithKline in Zebulon is seeking an experienced Production Operator to lead equipment changeovers and manage production activities. The role requires a minimum of 5 years in production and a strong understanding of SOPs, safety, and GMP standards.

Ideal candidates will have experience in regulated environments and be comfortable working on-site in a dynamic manufacturing setting. The position offers opportunities for training and development.

Qualifications

• Minimum of 5 years of experience in a production or process operator role.
• 3+ years of experience in a regulated manufacturing environment.
• Experience performing equipment changeovers and start‑of‑batch activities.

Responsibilities

• Lead equipment changeovers and start-of-batch activities.
• Monitor process performance and product quality.
• Complete accurate daily production records.

Skills

Production experience

SOP adherence

Equipment changeovers

Basic data skills

Education

High School Diploma or GED

Associate degree or technical certificate

Tools

MS Office

Job description

Responsibilities

• Lead equipment changeovers and start‑of‑batch activities with accurate documentation and safe handover.
• Operate, clean and maintain production equipment following SOPs and batch documentation.
• Monitor process performance and product quality. Escalate issues and support root‑cause resolution.
• Use production systems and basic data tools to record performance, identify trends and support improvements.
• Coach and train colleagues on safety practices and procedures.
• Support continuous improvement activities to increase safety, quality and equipment efficiency.
• Prepare production equipment and materials in line with batch instructions and SOPs.
• Operate machinery and perform processes for machining, chemical processing, formulation, visual inspection, assembly or packaging.
• Monitor meters, gauges, valves, temperatures and pressures to ensure adherence to production specifications.
• Meet production schedules, volume, cost and quality targets while maintaining compliance with safety and GMP standards.
• Handle, move, pack and sort raw materials and finished goods, ensuring efficient material flow. Monitor output quality, identify and elevate defects, and make necessary process adjustments.
• Complete accurate daily production records for traceability and performance analysis. Perform minor maintenance, troubleshoot equipment malfunctions, and collaborate with maintenance teams as needed.
• Maintain rigorous safety, hygiene and compliance standards to support inspection readiness and operational excellence.

Basic Qualifications

• Minimum of 5 years of experience in a production or process operator role.
• 3+ years of experience in a regulated manufacturing environment, or equivalent experience.
• High School Diploma or GED.
• Experience performing equipment changeovers and start‑of‑batch activities.
• Demonstrated experience following and completing batch documentation and SOPs.

Preferred Qualifications

• Associate degree, technical certificate or equivalent education.
• On‑the‑job training certification across multiple work centers.
• Practical mechanical aptitude and ability to read gauges and instrumentation.
• Basic computer skills including MS Office and experience using production systems.
• Experience using data to troubleshoot or improve process performance.
• Experience training others and contributing to written work instructions.

Physical and Workplace Expectations

• This position is on‑site and requires shift work in a regulated manufacturing environment.
• There is noise and moving equipment present.
• Workers are required to wear protective gear and equipment.
• Lift up to 40 lbs. and perform physical tasks on a daily basis such as kneeling, climbing and standing.
• Ability and willingness to work extended shift lengths (up to 12.5 hours) when needed. Ability to work shift patterns and overtime when required.

GSK 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 under federal, state or local law.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at [e-mail].