54 Job openings found

1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.60 LPA
Position:        QA Officer Location:       Silvassa Experience:    2 - 3 Years Industries:     Pharma  Responsibilities: Control sample verification Bmr bpr issurance, logbook Format issurance and sop preparation Documentation etc. Required Skills: Have good communication skills. Logical Thinking Organizing Required Qualification: - B.Sc/M.Sc - Chemistry Salary :- Upto 3.60 LPA If you are interested for this opening please send updated resume ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Monitoring all processes in process & FG quality results and trends  Reporting periodic status on quality function periodically and formats as defined to operations and top management  Maintaining all documents as defined for integrated QMS/ EMS/ TS  Undertaking RCA for recurring failure of processes / products followed by evolving CAPA in consultation with ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position:        QA Officer Location:       Vapi Experience:    2- 3 Years Industries:     Pharma API   Responsibilities: Responsible for document and data control activities  To prepare and update all master document list as per requirement. To initiate change control/document amendment for any change or improvement in the process. Review of BMR/BPR, APQR and QMS Documents Responsible ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 5.40 LPA
Job Description:1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.2. Preparation & Up-gradation of SOP, Specifications3. Maintain the Records of BMR, BPR, Batch Inspection Documents4. Maintaining Document & Record Control5. Preparation & Up-gradation of Routine Validation Protocol & Reports.6. Handling CAPA, Non- ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
Position:          Asst. Manager - Production  Location:         Silvassa  Experience:      8-10 Years Industries:       Pharma   Responsibilities: Daily Target Vs Actual monitoring. Final review of BMR/BPR Daily Production Report Yield Statement Filling of QMS documents Ensure smooth operations in all the production lines   Required Skills :- Managing people and equipment. Process safety knowledge Required Qualification: B.Pharm/M.Pharm/B.sC/M.sc - Chemistry Salary:- ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 3.50 LPA
Position:          IPQA Officer Location:         Vapi Experience:     2 -4 Years Industries:      Pharma Formulations  Responsibilities: To perform IPQA activities at shop floor in each and every stage of manufacturing and packing. QA overview for clean room behavior and personnel hygiene . Review of batch processing records. Review of all documents relating to the manufacturing, ...
1 Opening(s)
10.0 Year(s) To 13.0 Year(s)
8.00 LPA TO 14.00 LPA
Role & responsibilities 1. Handling Deviations / Change Control / CAPA / Incidence Reports / Training Records. 2. Handling MFR / BMR / BPR preparation and Review 3. Handling preparation of SOPs / Protocols / QMS. 4. Handling Documentation Control. 5.. Handling of SMF /VMP / Qualification 6. Should be able to handle audit compliance and ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 10.00 LPA
Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...
2 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Designation Shift Incharge Vacant Position 2 Department Production Location  Ankleshwar Education B.tech / B.E  - Chemical Required Experience 3 - 7 Yrs in Pharma Industry CTC Range 3.00 to 6.00 LPA Job Description production operations in intermediate/API utility operations, Equipment Handling, online BMR/BPR filling, Distillation process, having exposure of handling CF, multi mill, AGNFD, FBD equipment.
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...

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