95 Job openings found

1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
🔑 Key Responsibilities GMP Compliance Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities. Monitor day-to-day GMP activities and identify non-conformances. Support GMP audits (internal, customer, and regulatory). Documentation & Records Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers. Ensure proper documentation practices (GDP) are followed. Maintain training, deviation, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities Conduct routine chemical and physical tests on incoming raw materials, in-process samples, and finished products in accordance with SOPs and quality standards. Perform analytical techniques including titration, pH measurement, and instrument-based analysis (e.g., UV-Vis, chromatography as required). Accurately record, analyze, and interpret data; prepare test reports and maintain detailed laboratory documentation. Ensure ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.44 LPA TO 1.54 LPA
Job description Packing Chemist Officer Female 1 1 to 2 12th/BA Salary : 12000 to 13000 Location : Dadra & Nagar Haveli Required Candidate profile packing officer / supervisor having experience Perks and benefits As per industry Role Production & Manufacturing - Other Industry Type Pharmaceutical & Life Sciences Functional Area Quality Assurance Employment Type Full Time, Permanent Role Category Production & Manufacturing Education :  12th/BA UG :Graduation Not Required, Any Graduate
10 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
🚨 JOB DESCRIPTION – SYNTHESIS R&D 🚨 Company: Life Chem PharmaLocation: Panoli, Gujarat Position: Officer / Executive – Synthesis R&D Qualification: B.Sc. / M.Sc. Chemistry Experience: 2–8 Years in API / Pharmaceutical Synthesis R&D Key Responsibilities: Conduct laboratory-scale synthesis and process development for API and intermediates. Perform reaction monitoring, optimization, and yield improvement. Handle chemical reactions, work-up, isolation, ...
3 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.00 LPA
Internal Job Description Education / Experience  M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry  Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities  Technical skills &  Competencies / Language Technical competence.  Leadership skills.  Analytical ability.  Planning ability.  Communication skills.  Problem solving.  Team building.  KEY ACCOUNTABILITIES  Analysis and approval  Sampling, analysis and ascertaining quality of raw materials, packaging ...
3 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Skills & Technical Competencies ETP & Water Chemistry Expertise – Understanding of effluent treatment processes, chemical reactions, and biological treatment methods. Quality & Environmental Standards – Knowledge of statutory compliance, regulatory norms, and pollution control board (PCB) requirements. Analytical Testing & Equipment Handling – Hands-on experience with pH meters, spectrophotometers, BOD/COD testing, and ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities: Perform analysis of raw materials, in-process samples and finished products. Handle routine QC testing as per approved specifications and SOPs. Operate and maintain laboratory instruments and equipment. Prepare and maintain analytical reports, worksheets and QC documentation. Follow GLP, GMP and safety procedures. Support method validation, calibration and stability-related activities. Ensure proper sampling, testing and documentation ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities: Perform analysis of raw materials, in-process samples and finished products. Handle routine QC testing as per approved specifications and SOPs. Operate and maintain laboratory instruments and equipment. Prepare and maintain analytical reports, worksheets and QC documentation. Follow GLP, GMP and safety procedures. Support method validation, calibration and stability-related activities. Ensure proper sampling, testing and documentation ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Instrument handling knowledge like HPLC, GC, Karl Fischer, UV, particle size analyser, etc. Should have basic knowledge of formulation. Instrument handling knowledge like HPLC, GC, Karl Fischer, UV, particle size analyser, etc. Should have basic knowledge of formulation. Instrument handling knowledge like HPLC, GC, Karl Fischer, UV, particle size analyser, etc. Should ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities Perform testing of raw materials, intermediates, APIs and finished products Handle routine analysis using HPLC, GC, UV, IR, pH meter, KF, etc. Prepare and maintain COA, analytical reports, worksheets and laboratory records Follow GMP, GLP, SOP and data integrity requirements Ensure proper sampling, testing and documentation as per specifications Investigate OOS/OOT results and support ...

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