Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Oxford; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Senior Project Manager for their Sterile Manufacturing Centre of Excellence in Oxford. This remote position involves overseeing significant facility projects while ensuring compliance with strict regulations like GMP and fostering a culture of excellence and safety. Ideal candidates will have over 10 years of project experience in GMP environments and a strong understanding of sterile manufacturing processes.

Qualifications

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing.
• Strong track record leading large capital facility projects.
• Knowledge of sterile production and clean utilities.

Responsibilities

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

Skills

Project Management

Leadership

Stakeholder Management

Communication

Knowledge of GMP

Proficiency in MS Project

Understanding of Cleanroom Classifications

Job description

Senior Project Manager – Sterile Manufacturing Centre of Excellence, oxford district

Client:

Robert Half

Location:

oxford district, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

5

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

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.

If this is of interest please apply or send CV to [e-mail]

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Created on 26/06/2025 by JR United Kingdom