Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Warrington; Remote; GBP 45,000 - 85,000; Full time

Job summary

A leading company is seeking a Senior Project Manager for their Sterile Manufacturing Centre of Excellence in Warrington. This role involves leading complex pharmaceutical projects and ensuring adherence to strict GMP standards. The ideal candidate will have extensive experience in project management within the GMP environment of pharmaceutical manufacturing. This position is remote but UK-based, providing an excellent opportunity to contribute to impactful projects in the healthcare sector.

Qualifications

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing.
• Proven track record leading large capital facility projects.
• Deep understanding of sterile production and cleanroom classifications.

Responsibilities

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

Skills

Leadership

Communication

Stakeholder Management

Project Management

GMP Knowledge

Problem Solving

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, warrington, cheshire

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Client:

Robert Half

Location:

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.