98 Job openings found

1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 3.00 LPA
HPLC (Operation and Troubleshooting) stability study as per ICH Guideline. Dissolution apparatus operation and method development. AMV analytical method validation  analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.   To perform the daily calibration of Instruments/Equipments. To review raw materials, in process, intermediate, finished products, packing material, stability, ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 3.60 LPA
A Sr. Chemist QC (Quality Control) analyzes raw materials, in-process samples, and finished products using advanced techniques (HPLC, GC) to ensure quality, consistency, and regulatory compliance (GMP, ISO), requiring strong analytical skills, documentation, equipment management, and leadership to mentor junior staff and resolve complex quality issues. Key duties involve developing SOPs, ...
4 Opening(s)
7.0 Year(s) To 15.0 Year(s)
4.50 LPA TO 5.50 LPA
Hiring for Grade starches Pharmaceutical Products Manufacturing Industry Position: - QC Manager Education: MSc / BSc Experience: Min 7 years experience in Pharma Company Having good knowledge of QMS documentation like change control, deviation, CAPA, OOS, Qualifications, vendor handling.... etc Location: - Dondaicha – Nandurbar MH If you are interested kindly send your updated CV   For ...
4 Opening(s)
3.0 Year(s) To 8.0 Year(s)
2.40 LPA TO 5.00 LPA
Hiring for Grade starches Pharmaceutical Products Manufacturing Industry Position: - QC officer- Education: MSc / BSc Analytical Experience: 3 -5 years of experience in the pharmaceutical industry. Position: - QA Executive:- Education: MSc / BSc Experience: 4-6 years experience in Pharma Company Having good knowledge of QMS documentation like change ...
1 Opening(s)
20.0 Year(s) To 30.0 Year(s)
Not Disclosed by Recruiter
  Minimum 20 years in Quality Assurance/Quality Systems in API/pharmaceutical manufacturing, with significant exposure to regulated markets To provide strategic and operational leadership to the Quality function, ensuring robust implementation of quality systems, compliance with global regulatory requirements, and continuous improvement in all quality-related processes for API manufacturing. Key Responsibilities Quality Systems & Compliance Implement, ...
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)
15.0 Year(s) To 18.0 Year(s)
16.00 LPA TO 21.00 LPA
Position:        QA Manager Location:        Ankleshwar Experience:     15 - 18 Years Industries:     Pharma - API   Responsibilities: Day to Day planning and execution of various activities in QA Execution/review/Approval & monitoring of process validation activities. Preparation, review, Approval of process validation Protocol/Report. Preparation, review and Approval of Annual Product Reviews Handling of Change Controls ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 13.00 LPA
Position:          Dy. Manager - Quality Location:         Vapi Experience:      8 - 10 Years Industries:       Pharma API  Responsibilities: Quality Management System (QMS)   Establish, implement, and maintain an effective Quality Management System in line with cGMP, ICH, USFDA, EU-GMP, WHO, and other regulatory requirements. Ensure compliance with SOPs, policies, and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 6.00 LPA
Position:      QC Officer Location:       Dahej Experience:    3 - 4 Years Industries:     Pharma API  Responsibilities: Perform chemical and physical analysis of raw materials, in-process samples, and finished products as per approved specifications. Ensure testing is carried out in compliance with SOPs, GMP, and safety guidelines. Maintain accurate laboratory records, test reports, and logbooks. Calibrate, ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position:          Production Officer (Documentation) Location:         Vapi Experience:      5 - 8 Years Industries:       Pharma - API Responsibilities. Handling of QAMS, DMS activities Prepare SOP, BMR, ECR and all related docs. as per CGMP TO maintain & review all document like change control, Incident with compliance report Involvement in ...

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