Process & Validation Project ManagerLocation: Philadelphia, PAEmployment Type: Full-time, mostly onsiteAbout UsAre 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 a 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:Competitive SalaryComprehensive BenefitsCompensatory Paid Time Off (PTO)Paid Parental LeaveA Flexible Work Environment that values work-life balanceOpportunities for Professional GrowthResponsibilities and Duties:Plan, coordinate, and execute facility improvement projects, including scope definition, scheduling, contractor coordination, and closeout documentation.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.Identify and escalate project risks, scope changes, and schedule impacts in a timely manner, proposing mitigation strategies as appropriate.Ensure all project activities comply with applicable GMP regulations, site SOPs, EHS requirements, and local building codes.Qualifications:Bachelors degree in engineering field or relevant equivalent.Minimum 5 years of prior experience preparing and executing equipment qualification documents (IQ/OQ/PQ) required.Excellent knowledge of the Current Good Manufacturing Practices.Excellent communication skills - verbal, written, listening and interpersonal with the ability to transfer knowledge to others.Strong technical knowledge, relationship management, organizational planning, and project management skills.Ability to demonstrate a sense of urgency, flexibility, and accountability.Flexibility to travel to the client site as required.Preferred QualificationsPrior experience performing GxP risk assessments such as Functional Risk Assessments (FRA) or Failure Mode and Effect Analysis (FMEA).Experience in Aseptic Processing.Familiarity with Computerized Systems Validation and ISPE GAMP5 and 21 CFR Part 11.Send us your application today. We look forward to meeting you!The LAPORTE team
Process & Validation Project Manager in philadelphia at Unknown Company
This position is listed as contract and onsite.