Process Validation Engineer

LAPORTE is a consulting engineering firm specializing in pharmaceutical, agrifood, industrial biotech and industrial plant processes, which has been in business for 25 years. Today, the company has 25 offices across North America and Europe, and over 480 employees with a passion for engineering. We offer a stimulating environment where autonomy, collaboration and professional growth are at the heart of our daily work. We believe in a flexible working environment that values work-life balance while encouraging efficiency and creativity on a daily basis. Discover an employer who takes care of its greatest asset: its employees! Process Validation Engineer (a minimum of 5 years of experience required) Location: King of Prussia, PA Employment Type: Full-time, mostly onsite About Us 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 Engineer 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 Engineer is responsible for supporting the validation of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing sectors. The Process & Validation Engineer will ensure equipment, systems, and validation programs are compliant with a client’s global/site standards and industry practices. The Process & Validation Engineer will live near King of Prussia, 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 Salary Comprehensive Benefits Compensatory Paid Time Off (PTO) Paid Parental Leave A Flexible Work Environment that values work-life balance Opportunities for Professional Growth Responsibilities and Duties: Carry out all aspects of a validation project for our clients including: authoring and/or executing Validation Master Plans (VMP), User Requirements Specifications (URS), Risk Assessments (RA), Design Qualification (DQ), Factory Acceptance Tests (FAT), Site Acceptance Tests (SAT), Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Validation (PV) protocols/reports in accordance with corporate and departmental procedures. Validation Planning: Develop Validation Master Plans outlining the validation strategy, scope, and timelines for the project. Documentation Management: Oversee the creation, review, and approval of validation protocols, reports, and other documentation required for validation activities. Risk Assessment: Conduct Risk Assessments to identify potential validation issues and develop mitigation strategies to address them. Protocol Execution: Oversee the execution of validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for equipment and systems within the QC building. Commissioning Support: Collaborate with the commissioning team to ensure a seamless transition from construction to operation, verifying that systems and equipment are installed correctly and function as intended. Standard Operating Procedure: Provide technical input with respect to Standard Operating Procedures (SOP) development. Revise or develop SOPs in compliance with industry standards and cGMP. Support client Quality Assurance (QA) compliance teams by initiating change controls, documenting deviations, and contributing to the implementation of CAPA (Corrective and Preventive Actions) within validation activities. Perform Periodic Review for various validated systems including computerized systems, laboratory equipment, manufacturing equipment, and infrastructure systems. Analyze information, draw the right conclusions based upon technical knowledge of the systems, and work effectively with different groups across site to determine status, gaps, and corrective actions. Maintain up-to-date knowledge of validation requirements, practices, and procedures and coach other members of the team participating in validation activities. Maintain up-to-date knowledge of current GP (Good Practices, e.g. GMP/GLP) regulations, guidelines within North America (Health Canada, US Food & Drug Administration) and EU Eudralex. Maintain effective client relationships and act as a primary point of contact. Ensure that projects are implemented in accordance within the agreed scope, timelines and budget. 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 Qualifications Prior 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

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