Admiron Life Sciences – Multiple Openings (30+ Positions) in Quality Control Department
Greetings from Pranaya Group
We have an Urgent requirement in Admiron Life Sciences at Parawada, Visakhapatnam. for the following departments
- Preference will be given to those who can Join immediately and or willing to really relocate to Visakhapatnam
Department: QC (Bulk Drugs /API Experience)
Position: QC CHEMIST-HPCL Analysis
Experience – 2-5 years
Openings: 10
Location: Admiron Life Sciences Pvt. ltd, Visakhapatnam. AP
Qualification: B.Pharm and M.Pharm-Pharmacy, M Sc
Job Description:
- To perform AnalyticalMethod Validation Test assay, Degradation Products and Dissolution by HPLC.
- To perform Method Transfer and Verification activities as per SOP’s and STP’s.
- To prepare protocols and reports of Method Validation & Transfer.
- Handling instruments like HPLC, GC, ICP-MS, UV, FTIR, pH Meter, etc.
- To perform calibration of AMV instruments and review their documents.
- To perform cleaning validation.
- Exposure of Labware software (Empower 3, UV Pro)
Interested candidates can send their resumes to hr@admironls.in, hr.corporate@pranayagroup.com
Department: QC (Bulk Drugs /API Experience)
Position: QC Chemist- GC Analysis
Experience -2-5 years
Openings: 10
Location: Admiron Life Sciences Pvt. Ltd, Visakhapatnam. AP
Qualification: B.Pharm and M.Pharm-Pharmacy, M Sc
Job Description:
- Operates and maintains laboratory equipment and instrumentation required for cGMP analysis of samples.
- Prepares chemical solutions following standard operating procedures and appropriate testing methods.
- Operates and maintains Gas Chromatography and/or High Pressure Liquid Chromatograph.
- Keeps an inventory of laboratory chemicals and disposable equipment necessary for the daily functioning of the laboratory.
- Performs wet chemistry and raw material analysis as requested.
- Perform testing in accordance with specified methods.
- Document activities in accordance with cGMP.
- Maintains orderly work area.
Department: QC (Bulk Drugs /API Experience)
Position: QC Chemist -WET Analysis
Experience -2-5 years
Openings: 10
Location: Admiron Life Sciences Pvt. Ltd, Visakhapatnam, AP.
Qualification: B.Pharm and M.Pharm-Pharmacy, M.Sc
Job Description:
Analysis of samples by chemical method and online reporting of in process and intermediate samples and analysis of in process validation samples.
- Analysis of samples by methods using HPLC,.
- Thorough knowledge on handling Validation & calibration of HPLC.
- Knowledge on handling of OOS, Deviations, Incidents. Should have Knowledge on Wet chemistry.
- Exposure to regulatory audits. Should have the knowledge of cGMP and Good documentation practices.
Interested candidates can send their resumes to hr@admironls.in, hr.corporate@pranayagroup.com
Department: Quality Control (QC) (API)
- Position : Assistant Manager
- Experience : 10-15 Years
- Openings : 01
- Location : Parwada, Visakhapatnam Dist.
- Qualification : B.Pharm and M.Pharm, M.Sc
Job Description:
- Implementation of the GLP
- Regulatory knowledge & guidelines – GLP, Schedule M, ICH, WHO TRS etc
- Ability to maintain coordination with their internal and external stakeholder for their smooth and timely functioning & timely release of RM, PM, in-process, FG, & Stability samples.
- Ensure compliance to perform the Preventive Maintenance/AMC of laboratory associated instruments /equipment.
- Ensure scheduled preparation, review & approval of the SOPs, STPs, GTPs and analytical data sheets with respect to Quality control Lab.
- To carry out the review and approval of qualification validation/ Calibration data of the Quality control Instruments/equipment’s
- To carry out the activities related to Quality Management System for new installation of the new instruments/equipment (i.e. Change Control Requests / protocols etc.)
- To ensure cGMP & hygiene in laboratory. Reference Standard/ Working Standard management.
- Ensure the continuous supply management of, Reagents/chemicals/Columns/solvents and glassware in the Lab.
- Approval of analytical Data of Finished Goods, Stability, Raw materials, Packaging materials, Primary Standard and working standard.
- Management and handling of stability studies.
- Responsible for coordination with PPC for mfg plan & timely release/rejection.
- Responsible for procurement of Lab equipment/instrument and it’s timely.
- Qualification with complete documentation (i.e. URS, FRS, DQ, IQ, OQ, PQ)
- Responsible for coordination with IT department to ensure timely execution of CSV.
- Responsible for SAP, QM module application in QC.
- Responsible to maintain safety in lab.
For shortlisted candidate telephonic interview will be conducted.
Interested candidates can send their resumes to hr@admironls.in, hr.corporate@pranayagroup.com
