Multiple Vacancies for M.Pharm, B.Pharm at Stallion Laboratories

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Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control. The path of success lies in its belief of creativity and no negotiation with the quality of work. Stallion Laboratories is coming up with Unit II which is proposed to be UK-MHRA, EU GMP & PICS approved plant. With its approval. Stallion aims to enter regulated markets.

Officer
Experience : 1 to 3 yrs of exp
Qualification : B.Pharm / M.Pharm
Functional Area in QA : IPQA
Major Responsibility : Have experience in OSD IPQA in manufacturing, Sampling and line clearance, Online documents and Data Integrity verification.

Executive
Experience : 4 to 6 yrs of exp
Qualification : B.Pharm / M.Pharm
Functional Area in QA : IPQA
Major Responsibility : Have experience in OSD IPQA in manufacturing. Sampling and line clearance, Online documents and Data Integrity verification. BMR and BPR Review and Batch Release. PV Sampling Continuous process verification

Officer / Executive
Experience : 3 to 6 yrs of exp
Qualification : B.Pharm / M.Pharm
Functional Area in QA : Validation and Qualification
Major Responsibility : Working in OSD plant, direct exposure of Water validation, HVAC qualification, compressed air qualification, autoclave qualification, facility qualification. Production machine qualification. Experience in preparation of validation protocol. Process validation, temperature mapping. Hold time study.

Officer / Executive
Experience : 2 to 6 yrs of exp
Qualification : BSc/ B Pharm / M Pharm
Functional Area in QA : Document Management
Major Responsibility : Handlin of Documents control and issuance, BMR / BPR issuance, issuance of log card. Controlling of documents in soft and hard copies. Organising and management document storage area.

Officer / Executive
Experience : 2 to 6 yrs of exp
Qualification : BSc/ B Pharm / M Pharm
Functional Area in QA : AQA
Major Responsibility : Well versed with GLP practices. Review of audit trail. Review of QC analyst raw data like chromatogram
- Review of QC specification / MOA

Interested Candidate share your CVs with CTC on following email address: hrmanager@stallionlabs.com

Last Date : 13th November, 2020

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