3 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities:
Perform analysis of Raw Materials (RM), In-Process Samples, Finished Products (FP), and Stability Samples.
Operate analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, and Dissolution Apparatus.
Prepare and standardize reagents, solutions, and reference standards.
Maintain analytical records, laboratory notebooks, and test reports as per cGMP and GLP requirements.
Perform calibration and routine ...
2 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Quality Officer(Analytical)
Location: Dadra & Nagar Haveli - Slivassa
Experience: 3 - 4 Years
Industries: Cosmetic
Responsibilities:
Perform analytical testing of raw materials, intermediates, finished products, and stability samples.
Operate and troubleshoot instruments such as HPLC, GC, UV, FTIR, and dissolution apparatus.
Review analytical data ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 4.00 LPA
Key Responsibilities
Perform routine analysis of Raw Materials, In-Process Samples, Finished Products, and Stability Samples
Handling and operation of analytical instruments like HPLC, GC, UV Spectrophotometer, pH Meter, KF, etc.
Preparation and standardization of reagents, volumetric solutions, and test solutions
Maintain analytical records, logbooks, and documentation as per GMP/GLP requirements
Conduct chemical analysis as per ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
1 Opening(s)
0 To 2.0 Year(s)
1.80 LPA TO 2.40 LPA
Job Description :
26/03/2024
HPS/2024/173
Qc executive
Male
1
0 to 2
DME/B.Tech
Qc executive for Plastic sheet line : We need a guy who should manage quality control of incoming raw material, packing material, online qc inspection on the production line, Qc of finished goods, Qc reports and documentation. Should know about all about ISO.
HPLC (Operation and ...
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Experience/Technical Skills :
Should have work experience in ADL Lab /PD Lab
Should be aware about Method Development and Method Validation
Should have knowledge of HPLC and GC
Should have knowledge and Work experience in ADL/R&D /PD Lab for analytical exposure
Should have ability to draft/prepare specification from monograph
Knowledge of ICH will be more appreciated
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Experience/Technical Skills :
Should have work experience in ADL Lab /PD Lab
Should be aware about Method Development and Method Validation
Should have knowledge of HPLC and GC
Should have knowledge and Work experience in ADL/R&D /PD Lab for analytical exposure
Should have ability to draft/prepare specification from monograph
Knowledge of ICH will be more appreciated
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 7.00 LPA
Vacancy: 01 Location: VAPI- GUJARAT Experience: 8 to 13 Years Qualification: B. Sc/ M. Sc- Micro/ Biotechnology with FDA Approval (Preference) Job Description: The ideal candidate will possess strong technical expertise in analytical instrumentation, regulatory compliance, and quality systems, with hands-on experience in RM, PM, and FG analysis. Key Responsibilities ...
1 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities:
1. Quality System Management
Implement and maintain the Quality Management System (QMS) in compliance with ISO 17025 / GLP / GMP / NABL standards.
Prepare, review, and control QA-related documents such as SOPs, policies, forms, and records.
Ensure timely calibration, maintenance, and validation of laboratory instruments.
Conduct internal audits and coordinate external audits ...