Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Glasgow; Remote; GBP 60,000 - 85,000; Full time

Job summary

A leading company is seeking a Senior Project Manager for its Sterile Manufacturing Centre of Excellence in Glasgow. This role involves overseeing complex pharmaceutical facility builds, ensuring compliance with quality standards, and leading cross-functional teams to drive project success. Ideal candidates will have extensive GMP experience and a strong background in sterile production and project management.

Qualifications

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

Responsibilities

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

Skills

Leadership

Communication

Stakeholder Management

Project Management

GMP Knowledge

Automation Systems Knowledge

Education

10+ years in Project Management

Experience in GMP-regulated pharmaceutical manufacturing

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, Glasgow

Client: Robert Half

Location: Glasgow, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 4

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.