Senior Project Manager – Sterile Manufacturing Centre of Excellence

JR United Kingdom; Belfast; Remote; GBP 70,000 - 100,000; Full time

Job summary

Une entreprise de recrutement spécialisée cherche un Senior Project Manager pour un centre d'excellence en fabrication stérile. Le candidat idéal aura au moins 10 ans d'expérience en gestion de projets GMP dans la fabrication pharmaceutique. Le rôle requiert de diriger des projets complexes, respecter les réglementations et promouvoir une culture d'excellence et de sécurité. La position est basée au Royaume-Uni avec une flexibilité de travail à distance.

Qualifications

• 10+ années d'expérience en gestion de projets dans un environnement pharmaceutique réglementé.
• Compréhension approfondie de la production stérile et des classifications de salles blanches.
• Expérience avec des systèmes d'automatisation (SCADA, MES, BMS).

Responsibilities

• Diriger le cycle de vie complet d'une construction complexe d'installations pharmaceutiques.
• Assurer la conformité avec les meilleures pratiques GMP et Annex 1.
• Gérer la communication avec les parties prenantes et les attentes réglementaires.

Skills

Gestion de projet

Leadership

Communication

Gestion des parties prenantes

Compétences en anglais

Tools

MS Project

Job description

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Senior Project Manager – Sterile Manufacturing Centre of Excellence, belfast

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Client:

Robert Half

Location:

belfast, United Kingdom

Job Category:

Other

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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.