Unichem Laboratories Released Job Openings On 20/07/2022.Promoted by the late Mr. Amrut Mody, a pioneer of the Indian pharmaceuticals business, Unichem Laboratories has grown to become one of India’s most respected pharmaceutical companies. It is committed to deliver better health through superior products.
Vacancy Details:
Unichem Laboratories Recruiting B.Pharma, B.Sc,M.Pharm,M.sc Candidates with 15 – 18 years of Experience for QA / QC Manager Position.Complete Details for the QA / QC Manager as follows.
Important Details :
- Location :Roha
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 20/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Job Description/Skills Required
- Ensure all-time readiness’ for regulatory inspections by continuous monitoring of cGMP, GLP & regulatory norms.
- Continuously improve the existing systems / procedures as per quality system guidelines issued by CQA and various international guidelines including ICH.
- Perform self-inspection as per cGMP requirements and promptly reply to all inspectional observations of audits done by external agencies, customers, and CQA.
- Ensure that all committed compliances are completed within the timelines.
- Ensure that systems, equipment, personnel, processes, analytical methods, cleaning methods, utilities, facilities, etc. are qualified / validated as per requirement.
- Investigate out-of-specification results, and market complaints effectively, approve the CAPA, and ensure that identified Corrective & Preventive actions are executed.
- Review and approve qualification protocols / reports (DQ/IQ/OQ/PQ) related to Quality Control Instruments, Manufacturing Equipment, Computerized Systems, Utilities, etc.
- Review and approve all master documents and records like SOPs, VMP, and various Validation Protocols / Reports. Master Production Records (MPRs), Batch Production Records (BPRs), Stability Protocol / Reports, Quality / Technical Agreements, etc.
- Review, approve / reject, and close all Change Control / Deviation proposals / records and ensure that required Corrective / Preventive actions are executed as identified in the concerned record.
- Prepare, coordinate, and execute training schedules related to cGMP, GLP, and SOP.
- Release all finished API / intermediate batches including batches under invalid OOS / OOT / Deviation.
- Review and ensure that the preventive maintenance and calibration schedules are adhered to.
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