Manufacturing Project Manager

About the Opportunity

We are seeking a Manufacturing Project Manager with proven experience in equipment installation, commissioning, and facilitating cross-functional process engineering activities. This role will lead manufacturing projects from initiation through qualification, ensuring seamless execution in compliance with regulatory and operational standards.

Responsibilities

• Plan and manage equipment installation and commissioning projects in GMP-regulated manufacturing environments.
• Coordinate closely with process engineering, validation, maintenance, and operations teams to support process design, optimization, and implementation.
• Lead and facilitate IQ/OQ/PQ qualification activities for new and upgraded equipment and processes.
• Track and report project milestones, budget usage, risk registers, and resource allocation using PMO methodologies.
• Collaborate with external equipment vendors to manage FAT/SAT, site preparation, installation, and technical handover.
• Maintain clear communication with cross-functional stakeholders and provide regular updates to department heads and senior management.
• Ensure all project documentation complies with quality, safety, and regulatory requirements.
• Drive continuous improvement initiatives in project execution and manufacturing process efficiency.

Eligibility

Required Qualifications:

• Bachelor’s Degree in Mechanical, Manufacturing, Industrial Engineering, or related technical discipline.
• Level 8 degree in Mechanical, Manufacturing, Industrial, or Biomedical Engineering (or equivalent experience).
• Minimum 8 years of project management experience, with at least 4 years in manufacturing operations or capital equipment projects.
• Proven track record delivering $5M+ projects in highly regulated sectors.
• Strong knowledge of cGMP, equipment validation, and process engineering workflows.
• Experience leading or supporting IQ/OQ/PQ activities.
• Proven ability to coordinate multi-disciplinary teams and external suppliers.
• Excellent project planning, documentation, and communication skills.
• Proficiency in MS Project, Excel, and document control systems.

Preferred Qualifications:

• Experience in Pharma, Biotech, MedTech, or other regulated manufacturing environments.
• Familiarity with cleanroom operations, automation systems, or facility expansion projects.
• PMP certification or equivalent is a plus.

Benefits

Why Join NovintiX?

• Be part of a high-impact team driving innovation in the life sciences sector.
• Lead challenging, meaningful projects in world-class manufacturing environments.
• Grow your career with a company that values expertise, collaboration, and continuous improvement.