Senior Commissioning, Qualification, and Validation; CQV Engineer

Senior Commissioning, Qualification, and Validation (CQV) Engineer

We are searching for the best talent for a Senior Commissioning, Qualification, and Validation (CQV) Engineer to join our team in Spring House, PA. This position is part of the Site Engineering Team, which manages automation, engineering/CQV, and maintenance for clinical labs, GxP warehouse operations, cell banking, and other GxP labs in Springhouse and Malvern, PA. The primary work location is Spring House, PA, supporting the qualifications associated with a highly automated CAR‑T Clinical Manufacturing facility and may require support at our Large Molecule Clinical Production Site in Malvern, PA.

• Ownership for the development and execution of the Project Validation Master Plan (PVMP)
• Support the writing and approval of URSs (User Requirement Specifications) for facilities, equipment and systems.
• Lead the writing and execution of Impact Assessments for equipment and facilities, IQ & OQ, and Re‑qualification, as well as PQ activities
• Ensure flawless execution of Commissioning, Qualification, and Re‑qualification works for manufacturing and laboratory equipment, execution systems, as well as facilities and utilities
• Ensure compliance with all applicable cGMPs, global regulatory requirements, safety, environmental regulations, SOPs, WI’s and Company policies and corporate standards
• Support investigations, deviations, corrective and preventive actions towards successful timely and compliant closure
• Lead CQV role in compliance inspections / audits within area of responsibility
• Provide leadership and act as expert in the field CQV
• Develop & maintain in‑depth understanding of the CAR‑T manufacturing processes (including sound scientific understanding), operational procedures and manufacturing environment (Facilities, Utilities, Equipment, Systems, Processes)
• Conduct risk assessments and develop mitigation strategies to ensure compliance and safety in operations.

• Bachelor’s degree in Engineering, Life Sciences, or a related field.

• Minimum 4 years of experience in CQV engineering within the pharmaceutical or biotechnology industry.
• In‑depth knowledge of current GMP standards and guidelines related to equipment, utilities, and facilities commissioning and qualification (e.g., ISO, EN, ICH, FDA, ISPE).
• Ability to prioritize and manage the workload and, as required, be able to manage shifting priorities based on critical deadlines so that business needs are always met.
• Service mentality and ability to proactively collaborate with teams and partners, working hands‑on on aspects of C&Q tasks, while identifying areas of improvement.

• Certification in CQV or related field (e.g., ASQ, ISPE).
• Experience with automated production systems and controls.
• Familiarity with the latest developments in Cell and Gene Therapy production processes/equipment.
• Experience with KNEAT paperless validation software.
• Knowledge of cell processing robotics and automation.
• Understanding of aseptic and cell processing techniques.
• Experience with equipment / systems commissioning/qualification/validation, process automation associated with cell therapy (CAR‑T) processes.

• For the first year of this assignment travel up to 25% of the time may be necessary to support FATs, OEM site visits, and/or other project requirements. After the first year, travel of up to 5% may be needed.

• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Career opportunities and continuous personal and professional development in areas of technology and leadership.
• Personal Development Plan – such as access to further education & training, mentoring and coaching, development opportunities on‑the‑job or through exciting projects.
• Be part of a strong global network of talent and expertise, with opportunities to learn or move to different cultures and work environments.
• Many employee benefits.
• We are an equal opportunities employer.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected under federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & J&J is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via