108 Job openings found

1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Location: IMT Faridabad Plant Education: A B.Sc. degree preferably in Chemistry, or diploma in related filed. A solid background and understanding of Chemistry is mandatory Computer proficiency- Microsoft Office , especially Excel Experience working in contract Laboratory considered an asset. Experience working with Pharmaceuticals Job description: Proficient in operating GC/HPLC/LC-MS/MS/GC-MS. Ensures that all work is carried out in compliance ...
1 Opening(s)
0 To 2.0 Year(s)
1.80 LPA TO 2.00 LPA
Position:           QC Chemist Location:          Mehsana Experience:      0 -2 Years Industries:       Pharma API Responsibilities: Responsible for Documentation work in QC Department Candidate must have knowledge of HPLC/GC  Responsible for manufacturing the batch as per MOM or BMR. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan. Testing of all raw materials, packaging materials, in-process products & finished products. HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Position:          QC Chemist  Location:         Vatva - Ahmedabad  Experience:     4 - 6 YEARS Industries:      Chemical Responsibilities: To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples. To calibrate, validate, or maintain laboratory equipment. To compile laboratory test data and perform ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 5.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan. Testing of all raw materials, packaging materials, in-process products & finished products. HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position:          Manager/Dy.Manager -QC (Reviewer) Location:          Daman Experience:      7-10 Years Industries:       Pharma formulation  Responsibilities: Review and evaluate QC test results, analyse data and related records generated by QC Team, identify discrepancies and deviations, analyse and resolve deviations, compliance with regulatory requirement, handle OOS, OOT, Have handled HPLC  preventive maintenance of lab equipment, take ...
15 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan. Testing of all raw materials, packaging materials, in-process products & finished products. HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
2 Opening(s)
5.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 5.00 LPA
Position:           Officer/Executive -R&D  Location:          Vapi Experience:      5 - 8 Years Industries:       Chemical Responsibilities: Responsible for Documentation work in QC Department Handling of GC/HPLC Responsible for manufacturing the batch as per MOM or BMR. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
 Position:         QC Analyst Location:         Daman Experience:     3-4 yrs. Industries:       Pharma    Responsibilities:         Sampling and testing of in-process and finished product. Responsible for analysis of FG, RM and PM as prescribed specification. Handling instruments like HPLC, GC, ICP-MS, UV, FTIR, pH Meter, etc. Ensure all the work is performed and document accurately & complies as internal ...
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 ...

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