1 Opening(s)
5.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QC(P)
Location: Vapi
Experience: 5 - 12 Years
Industries: Pharma
Responsibilities:
Analytical Operations:
Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG).
Operate and maintain analytical instruments:- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus
Ensure compliance with ...
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 ...
2 Opening(s)
7.0 Year(s) To 15.0 Year(s)
9.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QA
Location: Pariya - Vapi
Experience: 7 - 15 Years
Industries: Pharma
Responsibilities:
Monitor manufacturing and packaging processes, including line clearance and in-process checks (IPQA)
Manage documentation activities, including DOC-QMS systems, SOP preparation, deviation handling, and change control
Support Technology Transfer ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager - Operation Excellence
Location: Ahmedabad
Experience: 5 - 10 Years
Industry : Pharma
Responsibilities:
Classification of Inventories.
Understanding and implementation of lean manufacturing work practices including 5S, AM and problem solving (including root cause analysis), to drive continuous improvement activity throughout the site.
Ensure all training for direct reports is ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.50 LPA TO 3.50 LPA
Position: Officer/Executive - QA
Location: Pariya - Vapi
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines, FDA documentation requirements, and internal quality ...
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: ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Trainee
Location: Silvassa
Experience: Fresher
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
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 material.
To ensure ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: Packing Incharge
Location: Mehsana
Experience: 5 - 6 Years
Industries: Pharma
Responsibilities:
Supervise and control online packing operations in accordance with EXCiPACT standards, cGMP and FDA guidelines and company procedures.
Operate, monitor, and troubleshoot PLC, DCS, and SCADA systems to ensure smooth production processes.
Manage packing team ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Executive (Reviewer)
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma
Responsibilities:
Experience in Method Validation.
Experience in Stability Study.
Experience of review Electronic data review and backup systems.
Expert in Qualification of analytical instruments like HPLC, GC, AAS, FTIR, UV etc.
Expert in Calibration of analytical instruments like HPLC, GC, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Officer/Executive - R&D
Location: Vapi
Experience: 2 - 6 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 analytical ...