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Business Change Lead; PMO

Job in Zebulon, Wake County, North Carolina, 27597, USA
Listing for: GlaxoSmithKline
Full Time position
Listed on 2026-02-07
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Operations Engineer
Job Description & How to Apply Below
Position: Business Change Lead (PMO)
Location: Zebulon

Overview

Site Name: USA - North Carolina - Zebulon

Posted Date:
Feb 2 2026

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.

Position Summary

The purpose of this role is to project manage New Product Introduction (NPI) projects and activity on behalf of the Zebulon (Zeb) site to ensure that new products are successfully introduced.

New products to the Zeb. site is defined as:

  • New GSK products/chemical entities transferred from within GSK R&D (typically at Commit to Phase 3 / Commit to Filing and Launch Plans)
  • In-licensing and/or 3rd Party Contract Manufacturing of products for 3rd party manufacturers or 3rd party research organizations.
  • Global Supply Chain (GSC) / GSK business transfers. These are transfers of production from other GSC / GSK sites to Zeb.
Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Have overall responsibility for the successful project delivery of GSK Zeb. new products, product line extensions, in-licensed products, 3rd party contract manufacturing products and product transfers to the Zeb. site (also may have specified involvement in other strategically important site projects, where deemed appropriate).
  • Project management of allocated NPI projects through development, clinical trials, registration / stability batches and validation batches, culminating in launch and commercialization.
  • Ensure that the delivery of new products, line extensions and new technology is both successful and robust.
  • Development of project plans, and monitoring of adherence to plans, to achieve key project milestones, whilst developing appropriate contingency and securing suitable resources.
  • Represent Zeb. site and GSC (where required) on cross functional project teams led by GSK central / R&D groups or 3rd party organizations.
  • Lead on-site multi-disciplinary project teams to deliver projects, which typically consist of representation from multiple functions including quality, production, engineering, logistics, finance, microbiology, analytical and technical teams (team size may be up to 20 personnel dependent on size and scope of project).
  • Escalate any potential resource conflicts, capacity issues, supply challenges or technical difficulties to the Site Engineering, key stakeholders and / or Site Leadership Team (SLT) for support and resolution (and agree any off-site communication as appropriate)
  • Effectively communicate and/or escalate progress on key batch activities to central functions / off-site teams as agreed.
Why You?

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

  • Bachelor s degree in engineering, Pharmaceutical Sciences, Chemistry, Biology, or related field required.
  • Knowledge of product portfolios
  • Knowledge of technology transfer and Chemical Manufacturing and Controls process.
  • Knowledge of GSK commercial operations
  • Business and Technical expertise in a regulated industry program delivery
  • Experience with regulatory processes and their requirements for global markets and individual dose forms.
  • Experience leading on-site cross functional teams.

Complexity

  • This role will lead site-based project teams.
  • Significant levels of change-management on-site will be required.
  • Use of influencing…
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