Project Director
Technical Source has partnered with a client in the Greater Boston area to identify a pharmaceutical manufacturing project director for a 9 month contract on a capital project. Candidates should have deep experience in leading the greenfield and/or brownfield manufacturing projects.
Required Experience:
- Industry Experience: Minimum of 10 years of experience in project management within the pharmaceutical manufacturing industry, with a proven track record of successfully leading and delivering capital projects.
- Project Scope: Demonstrated experience in managing large-scale capital projects, including planning, execution, and closeout phases.
- Regulatory Compliance: In-depth knowledge and experience with regulatory requirements and standards in the pharmaceutical industry, including FDA, EMA, and GMP regulations.
- Leadership: Strong leadership experience, including managing and coordinating multidisciplinary teams, contractors, and suppliers.
- Budget Management: Extensive experience in budget planning, management, and cost control for large-scale projects.
- Risk Management: Proven ability to identify, assess, and mitigate project risks effectively.
Responsibilities:
- Manage various project services including Project Management, Project Engineering, Project Facilities Support, Project Quality Engineering, Plant Commissioning, Project Administration, Project Documentation Management, and CAD Services.
- Serve as the primary point of contact between client and the Project Execution Team.
- Oversee resource identification, onboarding, training, performance, and other HR-related issues.
- Ensure project staffing requirements are met and manage turnover if necessary.
- Own construction turnover to F&E, CQV, and Ops Readiness teams.
- Manage schedules for Pre-CQV Activities, including Equipment Readiness (Procurement, Receipt, Installation, Integration, Certifications, Calibration, CQV handoff, Transfer of Care Custody and Control).
- Oversee Commissioning Delivery for non-critical systems (facility and grey utilities).
- Manage Transfer of Care Custody and Control.
- Coordinate internal building impact and impairment.
- Manage Engineering Documentation (Registration Drawings, Facility and Utility Drawings, ETOPs, Lifecycle documents such as Impact Assessments and Sensor Risk Assessments).
- Own project work order generation, execution, closure, and process management.
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Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Project Management and Manufacturing -
Industries
Pharmaceutical Manufacturing
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Medical insurance -
Dental insurance -
Vision insurance -
401(k)
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