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    Senior Process Operator

    GSK
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    Job Details

    Location
    Zebulon, North Carolina, United States
    Posted
    4 days ago
    Job Type
    FULL_TIME

    Job Description

    İş Yeri: USA - North Carolina - Zebulon Yayın tarihi: Feb 16 2026 Job Title: Senior Process Operator As a Production Senior Process Operator, you will Operate, challenges and cleans equipment, according to appropriate to SOPs, JSAs, and batch documents to deliver high quality products manufactured in a safe way to fulfil the needs of the supply chain. Monitors equipment for excessive rejects. Performs all duties in accordance with regulatory and OSHA requirements. Ability to changeover and set up equipment to design specifications including performing all SAP changeover tasks. Identified as the SME for all systems interaction and operations and proficient at all SOPs, JSAs, and OSW for the relevant area documents. Leads the creation of standards/systems to increase business results.

    Key Responsibilities:

    Operates, challenges, replenishes consumable supplies, cleans equipment, and all the duties needed by the business in accordance with cGMPs, Batch Documentation, SOPs, ZSPs and JSAs as required and responsible for maintaining inspection readiness of area with minimal supervision. Actively participates and owns monitoring equipment for excessive rejects/ stoppages and utilizes performance data to escalate any problems occurring in the area that affects product quality, safety and other aspects of line performance.

    • Trained in the GSK Production System standards (i.e., 5s, standard work, problem solving, Gemba, process confirmations, and performance management) towards the goal of Zero Accidents, Zero Defects, and Zero Waste.
    • Participates in performance management entry, steps 1-3 of problem solving, and performing/maintaining OSW and 5S.
    • Delivers against safety, quality, waste & performance objectives defined by strategy deployment and identifies and recommends areas for process improvement or alternative operating methods to increase efficiency.

    Recognized as an expert on operations/process and possesses the ability to troubleshoot and resolve minor equipment production stoppages. Operator possesses considerable knowledge of the job and is reliable and able to produce high quality and high quantity work. Utilizes systems/applications required for job performance (i.e. DELTA, my Learning, Free Weigh, DISY, Active Plant, IP21, SAP basic transactions for meeting production supply, etc.).

    Works in coordination with other associates, assistants, and/or technicians to carry out daily job responsibilities, including recognizing and assisting with troubleshooting technical issues and providing information to the next supervisory level.

    • Demonstrates the ability to describe the technological theory of operation, product flow through equipment, and able to identify the function and purpose of all sensors, limit switches, and proximity sensors.
    • Demonstrates the ability to conduct equipment set up changeovers and start of batch activities to the designed specifications without start up issues. Ability to certify on multiple technologies and flow to the work as needed by the business.

    Why you?

    Basic Qualifications:

    We are looking for professionals with these minimum required skills to achieve our goals:

    High School Diploma or GED 5+ years experience in Production Operator role 3+ years experience working at GSK OJT certified in all work centers in packaging or the majority of work centers in manufacturing

    • Demonstrated performance in all Process Operator job roles

    Preferred Qualifications:

    We are looking for professionals with these required skills to achieve our goals:

    Associate Degree or equivalent education Basic reading, writing and mathematical skills Basic computer skills and understanding and operational computer skills, MS Word, and MS Excel. Ability to work accurately with figures and information Ability to use and analyze data effectively Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products

    Strong attention to detail and ability to create and follow detailed documentation. Ability to follow both written and verbal instruction.

    Skills:

    Basic reading, writing and mathematical skills Advanced computer skills and understanding and operational computer skills, MS Word, and MS Excel Ability to proficiently utilize basic hand tools Ability to work accurately with figures and information Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products

    Traits:

    Visual inspection and attention to detail Strong attention to detail and ability to create and follow detailed documentation. Ability to follow both written and verbal instruction. Thorough understanding of Overall Equipment Effectiveness Advanced computer skills (focused on MS Office) use software to analyze data & troubleshoot

    Ability to work independently Ability to train others on job related tasks Ability to set up equipment to scale measurements without assistance Competent at problem solving utilizing 6 step process that identifies root cause

    Physical Job Requirements:

    Ability to climb, kneel, stoop, balance, crawl, crouch, reach, sit, stand, walk, push, pull, grasp, feel, talk, hear, lift, and perform tasks as defined by the specific role. Ability to work overtime as needed. Must be able to wear gloves, eye protection, and protective clothing as required by the specific job role.

    Must be able to handle up to 40 lbs. of materials Must be able to work inside a manufacturing environment where there may be exposure to noise, moving mechanical parts, and various drug compounds as the specific role mandates. Must be able to flow to the work as needed and operate at a high energy fast-paced environment

    Ability to learn at a rapid pace to support training module expectations Ability to work up to 12.5 hrs. in one shift

    About the Zebulon Site:

    GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount and Wake Forest.

    Key differentiators about GSK and Zebulon:

    Our commitment to inclusion and diversity – we see diversity as a critical advantage of ours Our focus on cultivating a positive work environment that cares for our employees

    • Demonstrated opportunities for continued career growth driven by individual ambition
    • Leaders that care about their teams and growth of both individuals and the company

    A priority focus on Safety and Quality Clean and GMP compliant work environment Onsite cafeteria Onsite gym Temperature-controlled Licensed onsite Health & Wellness clinic #Earlycareers

    Work Environment This role is **on-site** and requires physical activity throughout the shift. You’ll work in a temperature-controlled manufacturing environment with protective gear provided. If you’re looking for a role where you can grow your career and contribute to a team that values safety and quality, we encourage you to apply!

    Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

    People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

    Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at HR.AmericasSC-CS@gsk.com where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

    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.

    Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

    Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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