Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Worcester; Remote; GBP 60,000 - 95,000; Full time

Job summary

A leading company is seeking a Senior Project Manager for a Sterile Manufacturing Centre of Excellence. This role involves leading complex projects in the pharmaceutical sector, focusing on compliance with GMP standards and stakeholder communication. The ideal candidate will have over 10 years of project management experience in sterile environments, demonstrating strong leadership skills and a commitment to excellence.

Qualifications

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

Responsibilities

• Lead the full lifecycle of a complex pharmaceutical facility build.
• Ensure compliance with GMP, Annex 1, and aseptic best practices in facility design.
• Drive a culture of excellence, safety, and continuous improvement.

Skills

Leadership

Communication

Stakeholder Management

Project Management Tools

Understanding of Sterile Production

Tools

MS Project

SCADA

MES

BMS

Job description

Senior Project Manager – Sterile Manufacturing Centre of Excellence, worcester

Client:

Robert Half

Location:

worcester, 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