Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Watford; Remote; GBP 60,000 - 100,000; Full time

Job summary

A leading company in the pharmaceutical sector is searching for a Senior Project Manager to lead the development of a complex sterile manufacturing facility. The role involves overseeing cross-functional teams, ensuring compliance with industry standards, and managing project risks. Ideal candidates have over 10 years of project management experience and a deep understanding of sterile production systems, along with strong leadership and communication skills.

Qualifications

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

Responsibilities

• Lead the full lifecycle of complex pharmaceutical facility builds.
• Ensure compliance with GMP and aseptic best practices.
• Drive a culture of safety and continuous improvement.

Skills

Project Management

Leadership

Communication

Stakeholder Management

Knowledge of GMP

Understanding of Sterile Production

Proficiency in Project Management Tools

Experience with Automation Systems

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, Watford, Hertfordshire

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Client:

Robert Half

Location:

Watford, Hertfordshire, 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.