Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Portsmouth; Remote; GBP 55,000 - 85,000; Full time

Job summary

A leading company is recruiting a Senior Project Manager for the Sterile Manufacturing Centre of Excellence in Portsmouth. This role involves overseeing the complete lifecycle of pharmaceutical facility projects while ensuring compliance with industry standards. The ideal candidate will have extensive project management experience and a deep understanding of sterile production processes, leading cross-functional teams to drive project success.

Qualifications

• 10+ years of project management experience in GMP-regulated pharmaceutical manufacturing.
• Proven track record in leading large capital facility projects.
• Fluency in English and strong leadership skills.

Responsibilities

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

Skills

Leadership

Communication

Stakeholder Management

Tools

MS Project

Job description

Social network you want to login/join with:

Senior Project Manager – Sterile Manufacturing Centre of Excellence, Portsmouth, Hampshire

col-narrow-left

Client:

Robert Half

Location:

Portsmouth, Hampshire, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

3

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 sterile.
• 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.