Corporate Quality Assurance
Bliss Gvs Pharma
- Posted: 3 months ago
- Openings: 10
- Applicants: 0
Job Description
Role & responsibilities
- Review of Analytical Method Validation/Verification related documents
- To Participate/Lead in investigations related to analytical documents.
- Monitor investigations and root cause identification for non-conformance and verification of action plan.
- Review of specifications, test procedures, analytical raw data, method development / validation data, stability documents and other analytical documents.
- Good knowledge of QMS systems such as Change control, Deviation, Market Complaints & CAPA.
- Experience of working in AQA / QC /ARD environment
- Proficient in MS Word, MS Excel.
- Good communication and inter-personnel skills.
- Proactive approach to problem solving.
More Info
Education
Any Graduate
Not Disclosed
Required Skills
CQA
Formulation
Quality
Assurance
Quality Assurance
Corporate Quality Assurance
Corporate Audit
Corporate
Contact Details
Bliss Gvs Pharma
+91 987654567
info@blissgvs.com
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