Bsc ,Msc ,B.pharm,M.pharm Graduates Walk In 7th Nov 2022 At Sovereign Pharma. Sovereign Pharma is a part of Dadachanji Group companies and is a quality-focused and WHO-GMP Geneva certified manufacturing facility for terminally sterilized and aseptically filled injectables, Sovereign Pharma was established in Daman in the year 2003 as a Contract Manufacturing Organization (CMO), supplying quality products to companies worldwide. With a production capacity of around 350 million pieces per annum, Sovereign Pharma manufactures and sells over 1 billion injection doses annually.
Sovereign Pharma Pvt. Ltd invites Freshers & Experienced Dynamic & Self-Motivated Professionals for the below positions at the Valsad, Vapi, Daman & Diu location. Job Openings for Bsc / Msc (Chemistry) B.pharm/ M.pharm Graduates.
Sovereign Pharma Pvt. Ltd is recruiting for the accompanying positions:
-QC- Officer / Senior Officer / Executive
Refer Notification & all relevant information below. Interested and qualified applicants can attend at scheduled time.
Related Job:Walk In Interview 5th Nov 2022 At Aizant Drug Research Solutions
B.sc,M.sc,B.pharma,M.pharma,B.tech,Diploma,10th,12th,Graduate Jobs
Opportunity subtleties:
Post Name:QC- Officer / Senior Officer / Executive
Capability:Bsc / Msc (Chemistry) B.pharm/ M.pharm
Experienced:02 to 7 years
Salary: 2,00,000 - 7,00,000 P.A.
Set of working responsibilities:Sovereign Pharma Pvt. Ltd Hiring For QC- Officer / Senior Officer / Executive !
Significant Details :
Place: Valsad, Vapi, Daman & Diu
Walk in Interview Date:7th Nov 2022
Time: 10.00 AM - 3.30 PM
Walk In Address:Sovereign Pharma Pvt. Ltd. | Survey No. 46/1-4, Kadaiya Village | Nani Daman - 396210 (view on Map))
Contact -Meryl Clews ( 02606635366 )
Related Job:Walk In Interview 5th Nov 2022 At Neuland Laboratories
Choice Process: The determination will be based on Interview.
Set of working responsibilities:
Hands on experience on HPLC /GC. Handling of instruments like Autotitrator, UV and IR. Wet and Dry analysis. Analysis of Raw materials, Finished Good and other analytical samples Review of RM, FP, Stability, calibration reports. Planning and execution of analytical samples. Investigation of deviation PCC, OOS, Job incident etc. Revision of reports received from CTL. Regulatory compliance.




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