Project Manager

Overview:

We are seeking an experienced Project Manager to lead a DeltaV automation project within a pharmaceutical manufacturing environment. This role requires strong leadership across global teams and a deep understanding of GMP-regulated automation projects, ensuring compliance, quality, and on-time delivery.

Key Responsibilities:

• Lead the full lifecycle delivery of a DeltaV automation project in a GMP pharmaceutical facility.
• Manage and coordinate a 25–30 person project team, including approximately 15 offshore and onshore resource.
• Ensure all project activities comply with GMP, GAMP 5, and pharmaceutical quality standards.
• Oversee project planning, scheduling, budgeting, and risk management in a regulated environment.
• Act as the primary liaison between automation, engineering, validation, quality, and business stakeholders.
• Drive effective communication and alignment between onsite and offshore teams.
• Support and oversee CSV / automation validation activities in line with pharma requirements.
• Ensure documentation, change control, and audit readiness throughout the project lifecycle.

Required Experience & Qualifications:

• Minimum 10 years’ experience in project management within pharmaceutical automation or regulated manufacturing.
• Proven delivery of DeltaV projects in GMP-compliant environments.
• Demonstrated experience managing large, distributed onshore/offshore teams.
• Strong understanding of GMP, GAMP 5, CSV, and FDA/EU regulatory expectations.
• Ability to work onsite and lead cross-functional teams in high-compliance setting.
• Excellent stakeholder management, leadership, and communication skills.