Manufacturing Specialist

Site Name:

USA - Pennsylvania -

King of Prussia Posted Date:

Apr 16 2026 The Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Culture (Ambitious for Patients, Accountable for Impact, and Do the Right Thing) on a daily basis by engaging positively with team members and production support groups. The manufacturing specialist, with support from the senior specialist and/or production manager, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role can support includes Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Demonstrate GSK Values - Patient Focus, Transparency, Respect, and Integrity - in every interaction, in every work task, and with every responsibility of the job role. Live GSK's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace. Engage in cross functional teams, using operational knowledge and project management skills prioritize improvements that simplify both technical (equipment, biopharm processes) and business systems (quality systems, logistics, etc). As a leader, ensures the team has appropriately prioritized these initiatives and is developing the capabilities to execute them. Understand production equipment and electronic systems in use and P&ID diagrams of production equipment, as well as site quality processes (deviation, CAPA, change control). Serve as technical experts for the production process and owners of production equipment. Own interactions between the production team and other departments, understanding impact of their needs versus the production schedule. Balance the team's ability to lead day to day operations with the consistent project management of programs and systems that need improvement over the long term. Adhere to safety procedures and training requirements in accordance with site, GSK, and federal regulations including the proper use of controls, personal protection equipment, and waste handling practices. Escalate equipment and processing issues that pose a safety or compliance risk Follow ALCOA (Attributable, Legible, Contemporaneous, Original, Accurate) principles for all documentation of performed tasks. Own deviation investigations, write-ups, and management of corrective and preventative actions, impact assessments, and simple change controls. Interact with agency (FDA, EMEA, etc.) auditors when required. Schedule and track activities which (directly or indirectly) impact the schedule of manufacturing and/or required documentation. Manage inventory of raw materials and single-use components, execute Batch Document revisions, and perform the role of Lead Investigator through the use of Enterprise Resource Planning (ERP) systems at site. For new product introduction (NPI) - During Engineering, PPQ, Clinical or Commercial manufacturing campaigns: train on and perform GMP operations in the seed lab (aseptic processing), cell culture, media and buffer prep, equipment prep, purification, and final fill (aseptic processing) production areas based on standard operating procedures (SOPs) and digitalized technologies. Support the coaching and training of operators and associate specialists in these processes. Expectation is that during manufacturing campaigns, this role spends up to 80% of time in the production suite, supporting operations directly as needed. Identify and implement processing improvements in operations, improvement to quality systems and ways of working, and required documentation updates within the controlled systems of the site. The manufacturing specialist will be responsible for availability as on-call personnel, remotely monitoring, and working during weekend coverage and some night coverage as needed. Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals: Bachelor's degree in a scientific discipline 2+ years of experience in a Good Manufacturing Practices (GMP) environment.

Preferred Qualifications:

If you have the following characteristics, it would be a plus: Working knowledge of quality systems: deviation, CAPA, change control, and control documentation demonstrated ability to work in a collaborated work environment #LI-GSK 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. 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.com 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/