110 Job openings found

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 ...
1 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Job Title: Warehouse Operator – Dispensing (Formulation Plant) Department: Warehouse / Stores – Dispensing Section (Formulations) 📍 Location: [Insert Location] 🕒 Experience: 2 to 5 Years 🎓 Qualification: B.Pharm / M.Pharm / Diploma in Pharmacy (Mandatory) Job Summary: We are hiring a dedicated Warehouse Operator – Dispensing for our Formulation manufacturing facility, responsible for precise ...
10 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
  Industry: Pharma Formulation Openings: 10Experience: 3–7 YearsPreference: Male Candidates only / Gujarati-speaking Key Responsibilities: Perform testing of Raw Materials (RM) & Packaging Materials (PM) as per pharmacopoeial standards. Ensure timely release of materials with accurate documentation. Follow cGMP, GLP, and regulatory compliance in QC lab. Maintain records, calibration logs, and SOP adherence. Coordinate with QA, Production, and Warehouse for smooth operations. Requirements: B.Sc./M.Sc. ...
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)
1.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below: To perform High Performance Liquid Chromatography analysis for various pharmaceutical tests including Related Substances, in compliance with 21 CFR Part 11 and cGMP guidelines. The role includes calibration, troubleshooting, integration, and data review activities related to HPLC.   Key Responsibilities: Perform routine and non-routine HPLC analysis for Assay, Related Substances, Content Uniformity, and other quality ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.00 LPA
Position:         QA Officer Location:        Ankleshwar Experience:    4 - 5 Years Industries:     Pharma   Responsibilities:         Ensure GMP compliant operations and robust Quality Management System (QMS) execution for API manufacturing at the Ankleshwar site, including documentation control, batch release support. Batch Documentation & Release: Review BMR/BPR, analytical reports, COAs; ensure compliance with specifications ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position:         Asst. Manager - QMS Location:        Ahmedabad Experience:    7 - 10 Years Industries:     Pharma Responsibilities: Handling of Change control Handling of Deviation Handling of Market Complaint Handling of OOS/OOT Handling of Corrective action and Preventive action Handling of Return goods & recall Handling of Failure investigation Quality Risk Management Review of Quality Agreement Vendor Qualification management Internal Audit ...

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