9 Job openings found

1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
 Position:          QC Manager  Location:          Vapi Experience:      8-10 YEARS Industries:       Pharma   Responsibilities:         Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 20.00 LPA
Position:          QC Manager Location:         Ahmedabad Experience:     10 - 12 Years Industries:       Pharma - Formulation Responsibilities: Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
1 Opening(s)
0 To 1.0 Year(s)
1.40 LPA TO 1.80 LPA
Position:          Trainee Microbiologist Location:          Daman Experience:       Fresher Industries:       Pharma  Responsibilities: GOOD KNOWLEDGE OF MICRO  WATER VALIDATON  AREA MONITORING  ROUTINE ANALYSIS OF SAMPLE. VALIDATION OF MICRO AND PREPARATION OF PROTOCOL   Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication.   Required Qualification: - B.Sc/M.Sc ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 8.50 LPA
Position:          Sr. Executive/ Asst. Manager - QA Location:         Vapi Experience:      8 - 12 years Industries:       Pharma API   Responsibilities: QMS handling like, change control, deviation, market compliant, returned product, SMF, Quality manual, VMP, and  New BMR , BPR preparations or revisions. Audit work ,preparation for compliance ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
13.00 LPA TO 15.00 LPA
Position:           Manager Microbiology Location:          Daman Experience:      5 - 10 YEARS Industries:       Pharma Responsibilities: Experience in vaccine and biological (Mabs) manufacturing, Handled greenfield / brownfield – Microbiology lab, qualification and validation of Microbiology lab and instruments, preparation and review of all Microbiology documents such as SOPs, protocols, reports, etc., USFDA and EU ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Position:          QC Head  Location:         Jhagadia near by Ankleshwar  Experience:      10 - 15 Years Industries:       Pharma   Responsibilities:         Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 9.00 LPA
Position:          Sr. Executive/Asst. Manager - QA Location:         Ahmedabad Experience:     8 - 10 Years Industries:      Pharma-Formulation Responsibilities: Shall be Responsible for ensuring Good Laboratory Practices compliance in Quality Control department. Handling of out of Specification (OOS), Out of Trend (OOT), Out of Calibration (OOC) and Lab Event investigations. Sporadic Review of stability. PM, RM, ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position:            Microbiologist Location:           Sarigam near by vapi Experience:       3 -4 Years Industries:        Pharma Formulaction  Responsibilities: Good Knowledge OF micro  Water validation  Area monitoring  Routine analysis of sample. Validation of micro and preparation of protocol   Required Skills Logical thinking. Organizing. Good in communication.   Required Qualification: - B.Sc/M.Sc - Microbiology Salary :- Upto ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 18.00 LPA
  Position:        QC Manager (Injectable) Location:          Daman Experience:     5 - 10 YEARS Industries:       Pharma Responsibilities: Experience in vaccine and biological (Mabs) manufacturing, Handled greenfield / brownfield – QC lab, qualification and validation of QC lab and instruments, Preparation and review of all QC documents such as SOPs, protocols, reports, etc., USFDA and EU audit handling exposure, ...

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