Site Name: Belgium-Wavre, USA - Pennsylvania - King of Prussia
Posted Date: Oct 22 2025
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
Are you ready to make a meaningful impact in a dynamic and highly regulated environment? As a Project Manager for Technical Life Cycle Management (TLCM) Incoming Material, you will play a key role in ensuring the continuous improvement and compliance of our processes and materials. You will collaborate with cross-functional teams to drive projects that enhance efficiency, quality, and sustainability. This role offers the opportunity to grow your expertise, lead impactful initiatives, and contribute to GSK’s mission of getting ahead of disease together.
Responsibilities
* Lead and coordinate Technical Life Cycle Teams (TLCT) to manage projects for incoming materials, ensuring alignment with GSK standards.
* Develop and implement continuous improvement projects, including preparing business cases and managing budgets.
* Maintain and share process and product knowledge across manufacturing, quality, and regulatory teams.
* Prepare and manage risk assessments for incoming materials, identifying opportunities for improvement.
* Act as a key contact during internal and external audits, providing expertise on processes and materials.
* Ensure compliance with quality and regulatory requirements while driving operational excellence.
Basic Qualifications
* Bachelor’s degree in a scientific or technical field (e.g., chemistry, bioengineering, life sciences).
* Minimum of 5 years of experience in biopharmaceutical manufacturing or related fields (e.g., QA, QC, regulatory affairs).
* Proven experience in project management, including leading cross-functional teams.
* Strong understanding of compliance requirements in a regulated environment.
* Excellent communication skills, both written and verbal, in English.
* Ability to analyze data and manage complex projects effectively.
Preferred Qualifications
* Expertise in managing incoming materials within a pharmaceutical or biopharmaceutical setting.
* Proficiency in French or other languages.
* Experience with continuous improvement methodologies (e.g., Lean, Six Sigma).
* Strong problem-solving and decision-making skills.
* Ability to influence and collaborate across diverse teams and stakeholders.
* Familiarity with project management tools and processes.
Work Environment
This role is based on-site in Belgium, offering opportunities for hands-on collaboration and leadership.
Ready to take the next step in your career? Apply today and join us in making a difference!
If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.
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