Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Shrewsbury; Remote; GBP 60,000 - 95,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Senior Project Manager for a Sterile Manufacturing Centre of Excellence based in the UK. The role is focused on leading complex facility projects, ensuring compliance with industry standards, and driving excellence across project teams. Candidates should have over 10 years of experience in GMP-regulated environments, with a strong understanding of sterile production processes.

Qualifications

• 10+ years project management experience in GMP-regulated pharmaceutical manufacturing.
• Experience leading large capital facility projects from concept to completion.
• Deep understanding of sterile production and cleanroom classifications.

Responsibilities

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

Skills

Leadership

Project Management

Communication

Stakeholder Management

Tools

MS Project

SCADA

MES

BMS

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, shrewsbury

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Client:

Robert Half

Location:

shrewsbury, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

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.