Project Manager, Technical Life Cycle Management, Incoming Material

GSK; Camden Town; On-site; GBP 50,000 - 70,000; Full time

Job summary

A global biopharma company is seeking a Project Manager for MSAT Packaging Operations in Camden Town, UK. This role involves leading projects that enhance efficiency and quality while ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor's degree in a relevant field, with at least 5 years of experience in biopharmaceutical manufacturing. Strong project management and communication skills are essential for success in this position.

Qualifications

• Minimum of 5 years of experience in biopharmaceutical manufacturing or related fields.
• Proven experience in leading cross-functional teams.
• Strong understanding of compliance requirements in a regulated environment.

Responsibilities

• Lead technical projects supporting qualification of primary packaging components.
• Develop and implement continuous improvement projects.
• Act as a key contact during internal and external audits.

Skills

Project management

Communication skills

Data analysis

Problem-solving

Education

Bachelor's degree in a scientific or technical field

Job description

Role Overview

Are you ready to make a meaningful impact in a dynamic and highly regulated environment? As a Project Manager for MSAT Packaging Operations, 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.

Key Responsibilities

• Lead technical projects supporting the qualification of primary packaging components for sterile products, 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.

Required 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.

Disability Accommodations

If you have a disability and require assistance during the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Why GSK?

Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company dedicated to creating an environment where our people can thrive and focus on what matters most.