Job Opportunity
A senior QA specialist is required to ensure compliance with GMP requirements.
The ideal candidate will possess a strong understanding of quality processes and systems, with experience in the pharmaceutical industry.
Key responsibilities include:
* Batch record review and material release, including Certificate of Analysis (CoA).
* Quality review and approval of Master Batch Record (MBR) for routine cleaning and process activities.
* QA review and approval of Standard Operating Procedures (SOPs), Work Instructions, and forms from other departments.
Requirements:
* Third-level degree in a science or pharmaceutical discipline.
* Minimum 3 years of experience within the pharmaceutical industry.
* Strong knowledge of quality processes and systems is essential.
Preferred Qualifications:
* Working knowledge of automation recipe updates.