51 Job openings found

5 Opening(s)
5.0 Year(s) To 15.0 Year(s)
4.00 LPA TO 15.00 LPA
Job Description:* To ensure all relevant quality related documents are prepared, approved, implemented and followed.* Assuring that the right quality products reach the customer.* To ensure critical deviations are investigated and resolved.* To lead the internal audits and external periodically and follow up actions for its Compliances.* To identify gaps ...
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 ...
3 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
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 Specification. To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.50 LPA TO 4.50 LPA
Education: M.Sc. Analytical ChemistryWork experience: require min 2 to 4 yearsPurpose Role: Responsible for analytical development activities for quality testing in QC lab.Work location: Khopoli in Mumbai Responsibilities:• Development of analytical testing procedures and practices for quality testing.• Analytical method development for new RM by using GC, GPC and HPLC.• Coordination ...
2 Opening(s)
2.0 Year(s) To 12.0 Year(s)
2.00 LPA TO 12.00 LPA
Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC Desired Candidate Profile HPLC, Analytical Skills ADL   Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC Analytical Method Validation as per ICH guideline. Method development. SOP preparation. Stability Studies. Method transfer.   Desired Candidate Profile HPLC, Analytical Skills   Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC Desired Candidate Profile HPLC, Analytical Skills
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
 Quality Control department functions for assuring the quality of all the batches manufactured,at every stage of manufacturing/processing excipients and drug products. Sampling, inspection & testing as per specifications of Raw material for release or rejection& its documentation. Sampling, inspection & testing as per specifications of packaging material for release ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
1.80 LPA TO 3.00 LPA
We have Urgent Opening for the following position:- Please take it on Priority and all candidates should be from chemical and pharma background.       1) R&D Officers(Number of Opening-4)/ 2) Deputy Manager/ Manager(Number of Opening-1) Required Qualification-M.sc Organic Chemistry Compulsory For officer minimum experience should be 3 to 7 Yrs and  for Assistant Manager /Manager minimum experience should ...
1 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
1. Position- R&D Chemist/Officer2. Qualification- M. Sc /M. Pharm3. Experience-3-4 yrs.4. Responsibility? Handling of analytical instruments like HPLC, UV, titration, pH meter, Rheometer etc? Carry out the analytical development, analytical method validation or analytical workand prepare the reports for bulk, finish and rawmaterials.? Prepare stability protocols, schedules and carryout the ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
8.00 LPA TO 9.00 LPA
Position:         Executive/Sr. Executive - Production Location:        Daman Experience:     10 - 12 Years Industries:      Pharma  Responsibilities: Manage day-to-day production operations, ensuring timely and efficient manufacturing. Ensure compliance with GMP, safety, and environmental regulations. Optimize production processes to improve efficiency, reduce costs, and maintain product quality. Monitor and control production schedules, ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 15.00 LPA
Position:          QC Manager (Biosimilars) Location:          Bhopal Experience:       8 - 10 Year Industries:        Pharma              Responsibilities:   Manage QC activities raw materials, in-process, and finished biosimilar products. Oversee analytical and microbiological testing (e.g., HPLC, ELISA, SDS-PAGE, Western Blot). Ensure compliance with cGMP, GLP, ...

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