Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.
Post : Assistant Manager Quality Assurance
Review of QMS documents (Change Control, Deviations, Exceptions, CAPA) for Hormone QC Facility. Investigation of OOS, OOT, non-conformance, Root cause analysis and CAPA. To initiate change control/document amendment for any change or improvement in the process.
Review of Stability study protocol, report, and summary reports. Responsible for Self-Inspection. Review of RM, PM & Finished product & stability specification Review of audit trail of chromatographic equipment’s. Review of GLP related documents. To ensure compliance in the QC laboratory. Preparation, review and revision of QC SOP’s, Validation Master Plan, Site Master File & QM Review of AMV protocol & reports. Review of documents related to microbiology laboratory. To ensure that calibration, PM of analytical equipment is performed as per planner To impart training in the QC laboratory. Effectiveness of the CAPA task.
M.Pharma / B.Pharma / M.Sc Minimum 8 Years’ Experience in solid dosage form- Tablets.
Person shall be well versed QMS elements, OOS /OOT investigation, review of analytical documents, Audit Trail and Microsoft Office Word/Excel
Experience : 8 years
Qualification : M.Pharma / B.Pharma / M.Sc
Location : Ahmedabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Assurance
End Date : 10th March, 2023
See All Other Jobs in our Database