Engineering Project Manager
External job listingat Metric Bio
Lead capital projects at a high-volume oral solid dose manufacturing site, from business case development through commissioning and operational handover.
Salary
Not provided
Location
Minneapolis, United States
Employment type
Full time
Workplace
Not provided
Engineering Project Manager
Minneapolis, United States
Job description
About the role
Metric Bio is partnering with a leading pharmaceutical manufacturer to appoint a Project Engineering Manager for capital projects at a high-volume oral solid dose (OSD) manufacturing site.
The role is responsible for delivering the site's capital investment program, from business case development and equipment selection through installation, commissioning, qualification, and operational handover.
Responsibilities
- Lead and develop a team of project engineers.
- Work cross-functionally with Operations, Quality, Validation, Maintenance, and external vendors to deliver strategic engineering initiatives.
Requirements
- Proven track record leading capital projects in a GMP pharmaceutical manufacturing environment.
- Strong people leadership experience.
- Expertise in manufacturing equipment, facilities, utilities, automation, and validation.
- Experience in oral solid dose manufacturing is highly desirable.
Key facts
- The role leads capital projects at a high-volume oral solid dose manufacturing site.
- Responsibilities include delivering the site's capital investment program and developing a team of project engineers.
- Oral solid dose manufacturing experience is highly desirable.
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Frequently asked questions
What does the role involve?
It involves delivering the site's capital investment program, from business case development and equipment selection through installation, commissioning, qualification, and operational handover.
What experience and expertise are sought?
The ideal candidate has led capital projects in a GMP pharmaceutical manufacturing environment, has strong people leadership experience, and brings expertise in manufacturing equipment, facilities, utilities, automation, and validation. Oral solid dose manufacturing experience is highly desirable.
Who will the role work with?
The role works cross-functionally with Operations, Quality, Validation, Maintenance, and external vendors.