Production

B. Pharm , M.Sc. , M. Pharm with 2-8 years of relevant experience in IPQA , validation , Documentation related activities in Oral Solid,Oral Liquid,Semi Solid dosages manufacturing facilities.

Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.

M.Pharmacy/M.Sc Chemistry B.Pharmacy; Having injectable experience of Shop floor Supervising Activities like Component Preparation, Aseptic Filling, Compounding Operations, BMR Review and QMS Exposure.

The applicant must have experience in pharma units approved by regulatory agencies like USFDA, MHRA etc.

Handle manufacturing skids, Fedegari autoclaves, Isolator lyophilizers, vial washing and tunnel, vial, ophthalmic ,PFS filling and aseptic filtration, FFS, CIP,SIP, filters, microsphere refiner, Active freeze drying System. Operation, cleaning, sterilization, qualification and maintenance of solution preparation systems.

Handling HPLC, UPLC and GC. Knowledge in handling empower 3 software. Experience from Regulatory approved Sites are preferred.

Online filling of the BPRs and records and performing jobs related to SAP, Operate equipment's reactor, Sparkler Filter, Candle Filters , Centrifuge, Dryers as per SOP

Dossier and document preparation as per CTD,ACTD and country specific guidelines, Review of dossiers, DMF and Technical documents, Answer query raised from regulatory authority, package insert, SmPC, PIL & MSDS preparation

B.Pharma, M.Pharma - IPQA; B.Tech, B.E Any stream in Nutraceuticals, Chemical, Pharma devices, Pharma equipments, FMCG, API, Packaging.