Project Manager (LVP)
On-site · Coplay, Pennsylvania, United States
Job Summary
Lead end-to-end project lifecycle for GMP-regulated construction and facility upgrade projects in pharmaceutical environments; manage scopes, budgets, schedules, risk, and change controls; coordinate cross-functional teams including Engineering, Validation, Quality, Operations, EHS, and Procurement; ensure compliance with FDA, GMP, OSHA; develop documentation (URS, design packages, commissioning plans, status reports, closeout packages); conduct site walks and safety audits; support commissioning and turnover; drive process improvements; bilingual English/Spanish; 10+ years in pharma/construction; Bachelor's in Engineering; PMP/CAPM preferred.
Required Qualifications
- Bachelor’s degree in Engineering (Mechanical, Electrical, Civil, Chemical, Industrial) or related field
- 10+ years of experience managing construction or capital projects in pharmaceutical, biotech, medical device, or similarly regulated industries
- Strong understanding of GMP, EHS, and validation principles
- Proven ability to manage contractors, negotiate scopes, and maintain project controls
- Experience with project management tools (MS Project, Primavera, or similar)
- Excellent communication skills in English and Spanish, with the ability to translate technical information clearly for diverse audiences
- Demonstrated ability to work in fast-paced, compliance-driven environments with multiple priorities
- PMP, CAPM, or equivalent certification
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