Process & Validation Project Manager

Excellent knowledge of the Current Good Manufacturing Practices.

Flexibility to travel to the client site as required.

Familiarity with Computerized Systems Validation and ISPE GAMP5 and 21 CFR Part 11.

Serve as the primary on-site liaison for all project-related activities, ensuring minimal disruption to GMP operations and maintaining a safe working environment throughout project execution.

Initiate, author, and shepherd change control records through the site quality management system (QMS) in accordance with GMP change control procedures.

Coordinate and support the vendor approval and qualification process for new contractors and service providers, partnering with Procurement and QA as required.

Develop and maintain project schedules, status trackers, and progress reports for review by site leadership.

Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a strong presence in North America and Europe, is seeking an

Process & Validation Project Manager

to join our growing team. With 25 offices and over 480 employees worldwide, we specialize in delivering innovative solutions for the pharmaceutical and food & beverage industries.

The Process & Validation Project Manager is responsible for leading the coordination of projects of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing sectors.

The Process & Validation Project Manager will live near Philadelphia, PA. They will be motivated to grow and excel with the support and direction from an interdisciplinary team of engineers. Become part of a supportive work environment that emphasizes team culture and empowering engineers with more responsibility, professional growth, and a work-life balance.

At LAPORTE, we offer: