Who we are
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point.
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
We would like to invite applications for the role of Quality Assurance Analyst at our site in Waterford. This is a perm role.
The Quality Assurance Analyst is responsible for developing, maintaining and implementing quality standards and systems which give assurance that products comply with product licences, specifications and cGMP’s.
A Day in the Life of our Quality Assurance Analyst
1. To review batch documentation ensuring it is completed right first time and in full, in accordance with product licences, specifications and cGMPs.
2. To prepare, review and approve documents and reports to ensure compliance with regulatory guidelines.
3. To archive QA batch documentation.
4. To complete post QP batch related activities for customers.
5. To review, maintain and audit documents and processes in an efficient and timely manner in order to meet customer requirements both internal and external and ensure schedule adherence.
6. To act as a point of contact for external customers and to ensure all customers’ requirements are met in a timely manner.
7. To identify and make recommendations for improvements as part of a team within or outside the department in order to eliminate non value added activities and ensure continuous improvement.
8. To carry out audits to ensure that all operational processes are carried out in compliance with the required standards conforming to Company GMP, GLP, SOP, Specifications and Validation requirements.
9. To provide support for complaint investigation response and approval.
10. To track and support the CAPA system to maintain site compliance.
Who we are looking for
Are you….
11. Educated to Degree Level in a science related discipline and/or relevant experience in the healthcare industry
Do you have….
12. Knowledge of cGMP, regulatory bodies, customer requirements and environmental procedures.
13. Knowledge of Company policies, procedures and standards
14. Knowledge of production and Lab process and systems.
15. Knowledge of internal customers and suppliers.
16. Auditing skills.
17. Report writing experience
18. Documentation completion experience
19. Problem solving skills and process improvement experience
20. Teamwork/Collaboration Skills
21. Excellent planning and organisation skills
22. Good problem solving skills