Officer (RM) - Warehouse (Pharma)

Department :- Stores (Warehouse)Designation :- Asst. ManagerSection :- Raw MaterialQualification :- Graduate/Post Graduate/Material Management Required Candidate profileDepartment :- Stores (Warehouse)Designation :- Asst. ManagerSection :- Raw Material

1Ensuring resources available BMR, Raw Material, Packing Material Manpower etc.)2Liaison with QC/QA/STORE/Eng. Dept. for solving of trouble shooting problem.3Implementation and monitoring of GMP Standard.4Reporting to higher authority.5Raw material, packing material issuance and receipt from RMS and checking of MRO and verification6Intermediate, Finished...

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...

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...

Responsible for store functions-Managing timely material issuing procedure, storage of RM,PM,Finished Product & Engg items, Material planning, Inventory Mgt, alternate use/Scrap disposal, documentation, material audit, Co-ordination with deps etc. Required Candidate profileGraduate (+DMM preferable) with 4-8 years relevant exp preferably in API/Bulk Drug/...

To perform In process, Intermediate, Process validation, Raw material, Packing material, Stability, Working standard and finished product chemical sample analysis with proper documentation.Registration off All stages sample in LIMS etc.Maintain of Inward register, instrument usage log books.Preparation and documentation of volumetric solution/regents.To...

Responsibilities:* Conduct BPR reviews* Ensure compliance with GMP & Change Control procedures* Monitor product quality through IPQA processes* Collaborate on BMR development and maintenance* Implement BPRs as neededFood allowanceAnnual bonusProvident fund

Role & responsibilitiesTo carry out the manufacturing operations of Specialty Chemicals / intermediate processes in the plant as per the standard operating procedure. Operation of DCS. Perform regular/periodic activities of GMP procedures established in the plant.Perform first line production and reporting faults on plant and equipment.Follow safety...

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...

Site HR Business PartnerDate: 14 Oct 2025Location: Dahej - Human ResourcesCompany: Sun Pharmaceutical Industries LtdJob Title:Sr. Manager – HR & AdminBusiness Unit:Global Human ResourcesJob GradeG9Location :DahejAt Sun Pharma, we commit to helping you "Create your own sunshine"— by fostering an environment where you grow at every step, take charge of...