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Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom

Slough

Remote

GBP 60,000 - 90,000

Full time

Yesterday
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Job summary

A prominent recruitment agency seeks a Senior Project Manager for a Sterile Manufacturing Centre of Excellence in Slough. The role involves leading the lifecycle of complex pharmaceutical projects, ensuring strict compliance with industry standards. Candidates must possess robust project management experience within GMP environments and have a proven record of large-scale facility projects.

Qualifications

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

Responsibilities

  • Lead the full lifecycle of a complex pharmaceutical facility build.
  • Oversee cross-functional teams and ensure compliance with GMP.
  • Drive a culture of excellence, safety, and continuous improvement.

Skills

Project Management
Stakeholder Management
Leadership
Communication

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, slough

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Client:

Robert Half

Location:

slough, United Kingdom

Job Category:

Other

-

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.
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