Company
You will be working for a US founded pharmaceutical group with global reach. They are investing globally in new manufacturing sites and are currently looking at recruiting into their Validation teams to support this exciting growth!
Responsibilities:
- Interface with Subject Matter Experts, Site and Area Management, Quality Assurance, and other client resources for key information for validation projects planning
- Draft initial program CSV planning deliverables such as Validation, Security and Test Plans
- Support Validation efforts as per Validation Plan and CSV document management plan expectations
- Support the generation of individual project CSV documents such as Project Validation Plan, Test Plan, and Electronic Testing Templates and objects
- Recommend improvements for consistency or compliance in CSV deliverables
- Ensure CSV documents comply with corporate Quality Standards and Practices, local templates, and electronic document management system properties and practices
- Provide CSV mentoring and guidance for automation and other functional SMEs and other team members
Required Skills:
- 10+ years working experience in CSV within the Pharmaceutical or a similar industry
- Previous Large Project/Program experience
- Electronic Document Management and Electronic Test Management experience preferred.
