What are the responsibilities and job description for the Validation Engineer position at Veritas Search Group?
This role requires candidates who are currently authorized to work in the U.S. without sponsorship, and C2C arrangements are not accepted. This role is fully on-site in Boston.
GENERAL POSITION SUMMARY:
The Validation Engineer role plays an active role in Commissioning, Qualification, Validation (CQV), and Requalification activities for Cell and Gene Therapy facilities. This individual is responsible for executing qualification protocols and collaborating with internal departments such as Engineering, Facilities Operations, IT, Quality Assurance, and Project Management throughout the project life cycle.
KEY RESPONSIBILITIES:
Responsibilities may include, but are not limited to:
- Develop and execute qualification and validation test plans and protocols.
- Ensure validation documents are aligned with current standard operating procedures (SOPs), applicable global standards, and cGMP guidelines.
- Coordinate with internal staff and external vendors to schedule and execute test plans.
- Collaborate with construction and operations teams to safely and effectively implement validation activities, when required.
- Partner with cross-functional stakeholders including Project Management, IT, Environmental Health & Safety (EHS), Security, Design, and Quality teams.
- Complete assigned training and maintain 100% compliance at all times.
- Promote a “right-the-first-time” culture across all documentation and validation processes.
- Foster strong cross-functional relationships to support project success and maintain a reputation for reliability and excellence.
MINIMUM QUALIFICATIONS:
- Open and adaptable to change in a dynamic environment.
- Bachelor’s degree in Engineering (Chemical, Biomedical, Industrial, Biotechnology) or a related field.
- 2–4 years of experience in CQV or equivalent professional experience.
- Ability to work independently with minimal supervision.
- Hands-on experience developing and executing validation protocols in a GMP-regulated industry.
- Experience with Kaye Validators and data loggers.
- Familiarity with applicable standards and guidelines such as GMP, ISO, GAMP, and ANSI.
- Strong analytical, troubleshooting, and technical problem-solving skills.
Please submit your resume and send to recruiters@vsearchgroup.com if you are interested. Thank you!
Salary : $57 - $66
