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 ...