Solution Prep Principal CQV Engineer​/Lead Validation Engineer

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world‑class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

We are seeking a CQV Engineer with hands‑on experience supporting solution preparation systems within biopharmaceutical manufacturing environments. This role will focus on solution preparation, buffer preparation and media preparation unit operations, supporting commissioning, qualification and validation activities to ensure systems are designed, installed, tested and qualified in compliance with cGMP and regulatory expectations. The ideal candidate will have strong experience across the CQV lifecycle, including authoring validation documentation, supporting equipment startup and commissioning activities, coordinating vendor testing and ensuring systems achieve operational readiness.

Experience working within digital validation platforms such as Kneat is highly desirable. This position requires an individual who can work independently while collaborating cross‑functionally with engineering, automation, vendors and quality teams to ensure successful project execution.

• Commissioning, qualification and validation of solution preparation systems used in biopharmaceutical manufacturing
• Author, review and execute CQV lifecycle documentation, including:
  • Commissioning test protocols
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Validation summary reports
• Ensure validation documentation complies with cGMP regulations and internal quality procedures
• Participate in system impact assessments, risk assessments and validation planning activities
• Provide technical support for solution preparation unit operations, including buffer preparation systems, media preparation systems, solution preparation tanks and mixing systems, single‑use mixing systems, and transfer and hold systems
• Support equipment startup and operational readiness for solution preparation processes
• Assist with troubleshooting and process verification during commissioning and qualification activities
• Support Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) for new equipment
• Coordinate with equipment vendors and system integrators to ensure systems are installed and functioning according to design specifications
• Participate in equipment startup, commissioning and operational testing activities
• Collaborate with engineering, automation, quality assurance and manufacturing teams to align project deliverables
• Assist with deviation investigations, change control processes and documentation updates
• Ensure CQV activities align with project schedules and operational readiness milestones
• Utilize electronic validation platforms such as Kneat to develop, manage and execute validation documentation and maintain data integrity, traceability and compliance within digital validation systems

• Bachelor’s degree in Engineering, Biotechnology, Life Sciences or a related technical field
• 10+ years’ experience in a role specifically supporting CQV activities within GMP‑regulated pharmaceutical or biotechnology environments
• Hands‑on experience with solution preparation,…