Overview
Role: QC Analyst
Type :12 month contract
Location:Waterford
Work Model : Fully Onsite
Job Responsibilities:
1. Review data generated in a timely manner in support of batch release and stability programs.
2. Experience with Empower is essential. Good attention to detail, can take ownership and prioritize their workload for deadlines.
3. Familiar with checking results against trend limits and specifications, can identify deviations and/or lab investigations.
4. Trending of data.
5. Track and identify the level of not right first time (NRFTs) events.
6. Suport the QC Laboratory and Management.
7. Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases.
8. In particular, close contact maintained with the Quality Compliance Specialists and QC team Leaders.
9. Maintain, update and issue control prints, methods, specifications and SOP's in compliance to pharmacopeial and regulatory requirements.
10. Assist with training of the analysts in areas of expertise and knowledge and in new methods, SOP's and updates.
11. Excellent Communication skills.
12. Initiative – be able to work in a self-directed manner to see issues through to completion.
13. Work with the team and should be able to prioritize the work.
14. Extensive knowledge of cGMP and GDP in a regulated environment.
15. Working knowledge of quality systems in a regulated environment.
16. Excellent accuracy and attention to detail.
17. Excellent interpersonal skills.
EET
If you would like to discuss this role in confidence, contact Harleen Tora/