What are the responsibilities and job description for the Quality Assurance and Validation Expert position at SciPro?
SciPro's Commitment to Quality
We are committed to delivering high-quality products and services that meet the needs of our customers. As a CQV Engineer, you will be responsible for ensuring the quality and compliance of our cell therapy manufacturing facility.
You will lead commissioning, qualification, and validation activities, as well as oversee multiple CQV projects. Your work will directly contribute to maintaining a safe, efficient, and compliant manufacturing environment.
Key Responsibilities:
- Perform commissioning, qualification, validation, and maintenance activities within the facility.
- Oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors.
- Lead and support quality investigations, CAPAs, and process improvements to enhance compliance and efficiency.
