Officer

Production Sr. Officer (Effervescent Tablets) with 3–7 years' experience andM.Pharm/B.Pharm/M.Sc./B.Sc. Chemistry. The role focuses on granulation, compression, coating, cGMP compliance, and production optimisation to ensure quality and safety.

Sr Production Officer -3-10Years in Effervecscent Tablets-Granulation, Compression and Coating plan,CGMP etc with salary pack of upto 7LPA and Dahej Location.

Designation: QC Officer / Executive -(Male)Qualification: B.Sc./ M.Sc./ B. PharmaExperience: 2–5 years of experience in QC department of API pharmaceutical industry.Industry: Pharmaceutical (API Manufacturing)Job Location: Dahej (Gujarat)Key Responsibilities:1.Perform analysis of raw materials, in-process samples, intermediates, and finished APIs using...

Taking charge from previous shift by checking BMR and status of plant/ batches for operation in shift.To ensure that status of other activity is as per log report while taking charge from Outgoing officer.During shift to ensure that GMP norms are strictly followed and to report superior inCase of any deviation understood.During shift ensure that follows...

Dear candidate,We have an openings with reputed power Industry for HSE officer Manager (FTE)Job type - OffroleJob Industry - Hydro powerCompany - MNCJob location - Dahej-GujaratInterested candidates may drop your cv to Please find the JD below.10 to 15 years of experience (5 years managing HSE in Hydrocarbon industry), must have Diploma in Safety or...

Responsible for handling P&A functions, Recruitment & Selection, Performance Mgt,Time Office & Payroll, IR/ER, online statutory payments, Administration, Govt. Liasioning, MIS, compliance of Statutory & ISO norms, Co-ordination with other depts etc. Required Candidate profileGraduate/Post Graduate with 4 to 8 yrs relevant working exp of HR & Admn functions...

Interested candidates are requested to share their resumes at for interview scheduling on 7th September 2025 at Hotel Ginger, Bharuch. Please note that it is mandatory to pre-schedule the interview before reporting at the venue.Key Responsibilities:Perform routine and non-routine analysis of raw materials, intermediates, finished products, and stability...

Responsible for Analysis of RM/ inprocess/ FP/PM Samples, Instrument Calibration, Instrument Qualification Protocols & perform Qualification activity(OQ/PQ), analytical record, analytical cleaning method validation of the API, Online SAP Activity etc Required Candidate profileM.Sc./B.Sc. with 4 to 8 yrs exp in QC of cGMP, USFDA, MHRA approved Bulk drug/API...

Responsibilities:Manage receipts, issues, and stock of raw materials, consumables & packing materials.Prepare GRN/MRN, maintain proper storage, tagging & FIFO system.Coordinate with purchase & vendors for timely procurement.Conduct stock verification & reconciliation with ERP/SAP.Support audits & ensure compliance with safety & statutory...

Perform AMD & AMV for API dosage forms, handle HPLC/GC, develop stability-indicating methods (ICH, USP, EP, JP), impurity profiling, forced degradation, residual solvent analysis, method transfer, troubleshooting & compliance with GLP/GMP.