Senior Project Manager – Sterile Manufacturing Centre of Excellence

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

Job summary

Robert Half is seeking a Senior Project Manager for a Sterile Manufacturing Centre of Excellence in Leeds. This role involves leading a complex pharmaceutical facility build with stringent compliance and safety standards. The ideal candidate will have over 10 years of project management experience in GMP environments and a strong track record of successful capital projects.

Qualifications

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

Responsibilities

• Lead the lifecycle of complex pharmaceutical facility builds.
• Oversee cross-functional teams, ensuring compliance with GMP and aseptic practices.
• Manage project risks and stakeholder communication.

Skills

Leadership

Communication

Stakeholder Management

Project Management Tools

Tools

MS Project

SCADA

MES

BMS

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, Leeds, West Yorkshire

Client: Robert Half

Location: Leeds, West Yorkshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

3

Posted:

26.06.2025

Expiry Date:

10.08.2025

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

Responsibilities:

• 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.

Qualifications:

• 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.