About the Company:
The firm is one of the top health care provider globally and supplying world class high quality trusted medicines helping the mankind to face numerous diseases and helping in ailment. The firm in India focused on many streams like GIT, Cardiology, Women health and Primary care.
About the Job:
Assistant Manager in QMS
M. Pharma/B. Pharma./M. Sc
Least 6 Years' Involvement with strong dose structure Tablets. Individual will be knowledgeable QMS components, survey of reports, Cycle Approval and Microsoft Office Word/Succeed
Followings will be the obligations of the position holder:
Arrangement, audit and modification of Sop's, Approval Ground breaking strategy, Site Expert Record and QM Treatment of QMS exercises (Change Control, Deviations, Exemptions, CAPA) for Chemical Office. Answerable for issuance, recovery , capacity and obliteration of record and information control exercises. Examination of non-conformance, market protest. Underlying driver investigation and CAPA. To get ready and update all expert report list according to necessity. To start change control/record correction for any change or improvement simultaneously.
Survey of BMR/BPR, APQR and QMS Reports Answerable for Self-Review. Answerable for Yearly item Quality Audit. Capability of specialist organizations. Survey of fine art. Survey of RM/PM and Completed item determination
Executive in Quality control
Set of working responsibilities:
Experience Required: B.Pharm/M. Sc. with 2-4 years of involvement with Substance and Instrumental examination QC (RM). applicant with openness of testing in Isolator will be liked. Knowledgeable with CAPA, GMP Documentation, ought to have openness to administrative reviews, for example, MHRA, USFDA and so on.
Followings will be the obligations of the position holder:
1. Examining of unrefined substance (Openness to testing in Isolator) according to characterized method of Value Control Lab of Chemical block.
2. To guarantee the appropriate cleaning of examining corner, testing utensil and aggregation of its records.
3. Investigation of Seller Endorsement Tests.
4. Natural substance tests shipped off external research facilities with appropriate documentation and its getting consistence.
5. Examination of Unrefined substance, Completed Products, and solidness tests according to characterized STP.
6. Arrangement of volumetric arrangement and normalization, readiness of reagent and pointer as and when required.
7. Naming on endorsed RM, Dismissed RM and connected with documentation.
8. Information section in SAP framework.
9. Planning and adjusting the practices and methods in accordance with the COBC necessities