Production Supervisor/First Line Leader

Site Name:USA - North Carolina - Zebulon Posted Date:Mar 17 2026Are you looking for an engineering role that allows you to leverage your technical knowledge in a state-of-the-art manufacturing environment? If so, this Production Manager position could be an ideal opportunity to explore.Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.About the Role As a Production Manager (First Line Leader) at GSK, you'll play a key role in ensuring the safe, efficient, and high-quality production of our products. You'll collaborate with cross-functional teams, drive process improvements, and foster a culture of safety and continuous learning. We're looking for someone who is passionate about leadership, thrives in a team-oriented environment, and is committed to delivering excellence every day.Key ResponsibilitiesSchedule and execute site equipment, facilities and utilities in a qualified stateDevelop strategies to meet requirements for the site master validation planPlan, organize and prioritize staffing as to manage the site Master Validation Plan for equipment, facilities and utilitiesDevelop and execute documentation and protocols required to support all changes to do the installation of new equipment and manufacturing processes as well as any changes resulting from factory maintenance activities or interventionsParticipate on the site Validation Governance Board in collaboration with other board members and stakeholders and set site wide strategiesMake fully informed decisions and provide compliance and technical solutionsProvide managerial oversight to the assigned team of Engineers to fully develop work potential, prepare for promotional opportunity and provide a sense of job satisfactionMaintain a solid understanding of current FDA, Current Good Manufacturing Practices (cGMP), corporate guidelines, and industry best practices for this field and implement these standards dailyResponsible for on-time compliance records of project engineering departmentManage department budget and support departmental, plant, and corporate goalsManage vendors and consultants to ensure that contracts contain appropriate technical specifications are delivered as requiredProvide technical expertise during regulatory auditsParticipate in site Operational Excellence initiatives and author, review, revise, or approve Standard Operating Procedures (SOP's) as requiredProvide technical support for utility systems including purified water systems, compressed air systems, chilled water systems and steam systemsBasic QualificationsAssociate degree in a science or engineering related discipline or 10+ years plus experience in an equivalent lead role such as Production or Maintenance Lead, etc.3+ years of experience of pharmaceutical processes, systems, equipment and applicable government regulations2+ years of leadership experience in a manufacturing environmentPreferred QualificationsBachelor's degree in mechanical or chemical engineeringExcellent knowledge of cGMPsStrong written and oral communication skillsProficient in equipment troubleshootingGood management skillsTechnical expertise in P&ID nomenclature, instrumentation and electrical wiring diagramsProficient in SAP (work orders, history, maintenance plans)Good knowledge of cGMPs, and experience in an FDA regulated environmentExcellent written and oral communication skillsExperience working in a highly regulated Good Manufacturing Practices (GMP) environmentExperience leading facility equipment programs and leading maintenance teamsLeadership experience in coaching and collaborative workingAbout 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, Wilson, and Wake Forest.Key Differentiators about GSK and ZebulonOur commitment to inclusion is seen as a critical advantage of oursOur focus on cultivating a positive work environment that cares for our employeesDemonstrated opportunities for continued career growth driven by individual ambitionLeaders that care about their teams and growth of both individuals and the companyA priority which focuses on Safety and QualityClean and GMP compliant work environmentOnsite cafeteriaOnsite gymTemperature-controlled climateLicensed, onsite Health & Wellness clinicWhat We Value We value people who lead with respect, curiosity and practical support. You will join a team that cares about safety, quality and career development. If you are ready to lead a maintenance team and make a measurable impact on supply reliability, please apply. We look forward to hearing from you.#LI-GSKPlease 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.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 - usrecruitment.adjustments@gsk.comGSK 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/ AgenciesGSK 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/#J-18808-Ljbffr