Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Colchester; Remote; GBP 70,000 - 90,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Senior Project Manager for their Sterile Manufacturing Centre of Excellence. This role, which is fully remote and for 6 months, involves overseeing complex project lifecycles and ensuring compliance with industry standards. The ideal candidate will have extensive experience in project management within GMP-regulated environments and a strong understanding of sterile production processes.

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, cleanroom classifications, and regulatory compliance.

Responsibilities

• Lead the full lifecycle of a complex pharmaceutical facility build.
• Ensure compliance with GMP, Annex 1, and aseptic best practices.
• Manage project risks, stakeholder communication, and regulatory expectations.

Skills

Project Management

Leadership

Communication

Stakeholder Management

GMP Compliance

Process Automation

Tools

MS Project

Job description

Social network you want to login/join with:

Senior Project Manager – Sterile Manufacturing Centre of Excellence, colchester

col-narrow-left

Client:

Robert Half

Location:

colchester, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

4

Posted:

26.06.2025

Expiry Date:

10.08.2025

col-wide

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.