Found Description
Roles & Responsibilities
- Lead and support commissioning, qualification, and validation (CQV) activities for assigned projects.
- Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
- Develop and execute validation protocols (FAT/SAT, IQ, OQ, PQ) for equipment and systems.
- Coordinate with cross-functional teams, including manufacturing, quality, and engineering, to ensure seamless project execution.
- Identify and resolve technical issues during commissioning and qualification phases.
- Support continuous improvement initiatives to optimize processes and enhance project outcomes.
- Bachelor's degree in Engineering or a related field.
- 5-7 years of experience in CQV, validation, and commissioning, preferably within the pharmaceutical or biotech industry.
- Strong understanding of GMP standards and regulatory ...