Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Luton; Remote; GBP 60,000 - 90,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Senior Project Manager for a 6-month contract to oversee the build of a sterile manufacturing facility. The role involves leading complex projects, ensuring compliance with industry standards, and driving continuous improvement across teams. Ideal candidates will have extensive experience in GMP environments and strong leadership skills.

Qualifications

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing.
• Proven track record leading large capital facility projects.
• Fluent in English and proficiency in project management tools.

Responsibilities

• Lead the full lifecycle of a complex pharmaceutical facility build.
• Oversee cross-functional teams and ensure compliance with GMP regulations.
• Manage project risks and stakeholder communication.

Skills

Leadership

Communication

Stakeholder Management

Project Management

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, luton, bedfordshire

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Client:

Robert Half

Location:

luton, bedfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

Robert Half is recruiting for a Senior Project Manager – Sterile Manufacturing Centre of Excellence.

ROLE: Senior Project Manager – Sterile Manufacturing Centre of Excellence

LENGTH: 6 Months

LOCATION: Remote - UK based

PAY: depending on experience

The Role

• Lead the full lifecycle of a complex pharmaceutical facility build, aligning scope, budget, and schedule with business goals.
• Oversee cross-functional teams and external partners (architects, engineers, consultants).
• Ensure compliance with GMP, Annex 1, and aseptic best practices in facility and system design.
• Manage project risks, stakeholder communication, and regulatory expectations.
• Drive a culture of excellence, safety, and continuous improvement across the project.

Who you are:

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing, ideally steriles.
• Proven track record leading large capital facility projects from concept to completion.
• Deep understanding of sterile production, cleanroom classifications, HVAC, WFI, and clean utilities.
• Strong leadership, communication, and stakeholder management skills.
• Proficiency in project management tools (e.g. MS Project), and fluent in English.
• Experience with automation systems (SCADA, MES, BMS).
• Exposure to isolators, RABS, and advanced aseptic technologies.
• Knowledge of sustainable facility design or energy efficiency practices.