1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: IPQA Executive / QA Executive Location: Vadodara (Corporate Office) Experience: 1–2 Years (Pharmaceutical Formulation) Qualification: B.Pharm / M.Pharm / M.Sc.
If you have hands-on experience in IPQA, QA, GMP, Documentation, Line Clearance, Batch Manufacturing Records (BMR), and Quality Compliance, we'd love to hear from you.
Position: IPQA Executive / QA Executive Location: Vadodara (Corporate Office) Experience: 1–2 Years (Pharmaceutical Formulation)
3 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Lab Chemist
Location: Jhagadia nearby Ankleshwar
Experience: 1 - 2 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)
1.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: Production Officer
Location: Daman
Experience: 1 - 5 Years
Industries: Pharma
Responsibilities:
Monitor and control daily production activities as per production plan.
Ensure manufacturing of tablets, capsules, syrups, or other formulations as per SOPs and GMP guidelines.
Supervise machine operation, line clearance, and production manpower.
Maintain batch manufacturing records (BMR) and production ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: QC Executive
Location: Vapi
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Responsible for documentation work in the QC Department.
Perform analysis using HPLC and ensure compliance with analytical procedures.
Operate, calibrate, maintain, and troubleshoot ICP-MS (Inductively Coupled Plasma Mass Spectrometry) instruments for elemental impurity and trace ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Perform line clearance and in-process checks.
Ensure compliance with cGMP, GDP, and SOP requirements.
Handle deviations, change control, CAPA, OOS, and OOT investigations.
Prepare, review, and update SOPs and QA documents.
Conduct GMP audits and shop floor inspections.
Monitor documentation and maintain data integrity.
Coordinate with Production, ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 1.80 LPA
Position: Lab Chemist
Location: Vapi
Experience: Fresher
Industries: Chemical
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of 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 activities and Procurement of the packing material.
To ensure the compliance ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsibilities: QA Executive
To assign control number of Change control, Deviation, CAPA, OOS, OOT etc.
To handle QMS related documents and its applicable Quality trends.
To review investigation reports for deviation, OOS, OOT, OOE & Market Complaint.
To coordinate for Internal Audit.
To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsibilities: QA Executive
To assign control number of Change control, Deviation, CAPA, OOS, OOT etc.
To handle QMS related documents and its applicable Quality trends.
To review investigation reports for deviation, OOS, OOT, OOE & Market Complaint.
To coordinate for Internal Audit.
To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...