Commissioning, Qualification & Validation Specialist (CQV)
Cencora View all jobs
- Juncos, PR
- Contract
- Full-time
- Support Commissioning, Qualification, and Validation (CQV) activities.
- Develop, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
- Assist with equipment startup and commissioning activities.
- Author and review validation documentation, including protocols, reports, and discrepancy resolutions.
- Ensure compliance with cGMP regulations, FDA guidelines, and internal quality systems.
- Participate in risk assessments and impact assessments related to validation activities.
- Support change control, deviations, and CAPA investigations when required.
- Collaborate with Engineering, Quality, Laboratory, Manufacturing, and Validation teams.
- Ensure compliance with Good Documentation Practices (GDP) and data integrity principles.
- 2+ years of experience in validation, commissioning, qualification, or regulated manufacturing environments.
- Knowledge of cGMP regulations and validation lifecycle.
- Experience supporting IQ/OQ/PQ execution or validation documentation.
- Strong technical writing and documentation skills.
- Manufacturing equipment
- Laboratory instruments
- Utilities systems
- Facilities or cleanroom environments