Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Cheltenham; Remote; GBP 60,000 - 85,000; Full time

Job summary

A prominent company is seeking a Senior Project Manager to lead a complex pharmaceutical facility build in Cheltenham. This role requires over 10 years of experience in GMP-regulated pharmaceutical manufacturing, focusing on sterile production and compliance. You will drive project success while ensuring regulatory standards and fostering a culture of excellence.

Qualifications

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing.
• Strong understanding of sterile production and cleanroom classifications.
• 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 standards.
• Manage project risks and stakeholder communication.

Skills

Project Management

Leadership

Communication

Stakeholder Management

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, Cheltenham

Client: Robert Half

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Views:

4

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: Cheltenham, UK (Remote)

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 sterile.
• 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.