Officer / Executive - QC Microbiologist (Male Candidate Only)

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...

Hiring Alert - Safety Officer Chemical Industry We are hiring for our reputed client in the Chemical industry for the position of Safety Officer Location Dahej Experience 4 to 5 Years Qualification B Sc M Sc with PDIS or ADIS Industry Chemical Pharma Manufacturing Preferred We re looking for candidates with strong safety...

Job Title QA QC - Quality Checker Quality Associate Location Dahej Gujarat About Company Established in 1995 we are a research-driven specialty chemicals manufacturing company with a strong commitment to quality and innovation Located 40 km from Vadodara our facility is ISO 22000 2005 and HACCP certified producing high-grade antioxidants...

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...

Analytical support at QC LAB RIL-DMD A for ETP3 plant- 1 ETP plant samples and PTA5 6 PET3 Effluent samples - Daily scheduled and unscheduled samples testing as per SOP 2 Routine weekly monthly scheduled effluent samples of PTA5 6 PET3 plants 3 Extra samples during plant up-sets trials 4 Retest check samples about 3 max ...

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 Analysis of RM/IP/FP/PM Samples, analytical reports & documentation, identifying deviations, stability studies, comply with regulatory requirements, Calibration & trouble shooting of Instruments, Audit, cGMP & GLP, Qualifn Protocols.. Required Candidate profile 4 to 6 yrs exp in API. Sound exp & knowledge of handling GC,HPLC, KF, IR,...

Key Responsibilities:Responsible for receipt, storage, handling, and issuance of raw materials as per GMP and company SOPs.Ensure proper documentation of all incoming and outgoing raw materials (GRN, COA, logbooks, stock registers, etc.).Perform physical verification of raw materials against invoices and COA.Monitor raw material sampling and coordinate with...

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.Responsibilities:Carry out routine production activities for Small Volume Parenterals (SVP) in compliance with cGMP and...

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...