1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 8.00 LPA
1. Review overall QC documents.2. Prepare training modules as required and provide training to QC staff.3. Initiate and approve analyst qualifications as needed.4. Approve COAs for water analysis from the microbiology department.5. Review microbiological analytical reports, raw data sheets, and inward registers for finishedproducts.6. Prepare and validate Excel sheet calculations.7. ...
1 Opening(s)
12.0 Year(s) To 18.0 Year(s)
20.00 LPA TO 25.00 LPA
Position: Sr. Manager - QC
Location: Ahmedabad
Experience: 12 - 18 Years
Industries: Pharma
Responsibilities:
Lead and oversee the entire Quality Control department operations.
Ensure compliance with cGMP, regulatory guidelines, and company quality standards.
Review and approve analytical methods, specifications, and validation protocols.
Supervise raw material, in-process, and ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Asst. Manager - QC
Location: Panoli near by Ankleshwar
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
To manage day to day activities of quality control.
To distribute QC related work as per production planning
Preparation & reviewing of QC SOPs.
To monitoring of all the Q.C. testing & its complete ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.10 LPA
Position: QC Trainee
Location: Dabhel - Daman
Experience: 0 - 1 Years
Industries: Pharma
Responsibilities:
Assist in sampling and testing of raw materials, in-process, and finished products as per approved specifications.
Learn and perform routine tests using analytical instruments (e.g., HPLC, UV, IR, pH meter, KF, etc.).
Support the ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API
Key Responsibilities:
Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines.
Manage QC documentation, including qc document review, SOPs, and analytical records.
Supervise laboratory activities such as RM, PM, in-process, and finished product testing.
Ensure timely calibration, qualification, and maintenance of ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Research Associate
Location: Vadodara
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Synthetic Chemistry / Lab Work
Perform multi-step organic synthesis of target molecules as per project requirements.
Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products.
Maintain accurate lab records and notebooks (ELN ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: ADL Executive
Location: Paria - Vapi
Experience: 4 - 8 Years
Industries: Pharma
Responsibilities:-
Develop and validate analytical methods for raw materials and finished products.
Operate instruments like HPLC, GC, UV, IR, and dissolution testers.
Prepare method validation protocols and reports as per ICH ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: Officer/Executive – RA
Location: Paria - Vapi
Experience: 2 - 5 Years
Industries: Pharma
Responsibilities:
Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions.
Handle full lifecycle of product registration including new submissions, renewals.
Review technical documentation: ...
2 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Lab Chemist
Location: Jhagadia nearby Ankleshwar
Experience: 0 - 3 Years
Industries: Chemical
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 ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Executive - R&D
Location: Vapi
Experience: 8 - 10 Years
Industries: Pharma
Responsibilities:
Design Route of Synthesis & Planning of Experiment for process development of Active pharmaceutical ingredient.
To develop the manufacturing process of APIs & Intermediates.
Process optimization, process validation, determination of critical parameters.
Synthesis, isolation, and characterization of impurities.
Analysing ...