About the Role
The GxP QA Validation Specialist will be responsible for managing GxP validation activities, ensuring compliance with regulatory requirements, and participating in project teams related to validation documentation.
Key Responsibilities:
* Manage GxP validation activities
* Ensure compliance with regulatory requirements
* Participate in project teams related to validation documentation
Experience in the pharmaceutical industry is preferred.
Requirements
The ideal candidate will have a BSc or equivalent qualifications, with strong reviewing skills and attention to detail.
This includes excellent analytical and problem-solving skills, as well as the ability to work effectively in a team environment.
Additionally, the successful candidate will have experience working in a fast-paced environment and be able to prioritize tasks effectively.
The candidate should also have a solid understanding of quality management systems and be familiar with relevant regulations and standards.