Quality Specialist - Ireland, Waterford - 11 Months Contract
Do you want to be involved with exciting pharmaceutical projects?
Our pharmaceutical client, a leader in veterinary vaccine development and production, has the largest centre in the industry worldwide and is a Centre of Excellence, employing more than 1000 people. They are looking to add a Quality Specialist to their team.
Essential Duties and Responsibilities:
1. Participate in and support the site PVC (Process Validation Committee), WVC (Water Validation Committee), CVG (Cleaning Validation Group), and EQVC (Equipment Qualification Validation Committee).
2. Approve validation documentation and ensure compliance with MMD policies, procedures, and guidelines. Maintain validation status following changes or modifications.
3. Support the implementation of site or capital projects by defining validation requirements and providing technical assistance as part of project teams.
4. Develop Validation Summary Reports and assist in creating overall Quality plans for major projects.
5. Collaborate with other departments in MMD and industry to predict future validation trends and identify best practices.
Desirable Experience:
- Assertiveness and excellent communication skills
- Experience with QMS systems
- Background as a Quality Assurance/Quality Specialist
- Strong written and oral communication skills, including persuasive abilities
If this role interests you, please apply now
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