129 Job openings found

1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 7.00 LPA
๐Ÿ”ง Key Responsibilities Operate tablet compression machines (rotary machines like Cadmach / Fette / Korsch etc.) Set up machines as per batch manufacturing record (BMR) Perform in-process checks (weight variation, hardness, thickness, friability) Ensure proper cleaning of machines and area as per SOP Handle changeovers and minimize downtime Maintain production records and logbooks accurately Follow GMP, safety, ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
๐Ÿ”‘ Key Responsibilities: โœ… Handle complete shift production activities โœ… Monitor batch charging, reaction parameters, filtration, drying & packing โœ… Supervise operators and contract manpower โœ… Ensure adherence to SOP, BMR & safety guidelines โœ… Maintain production logbook & shift reports โœ… Coordinate with QA/QC, Maintenance & EHS departments โœ… Handle ...
100 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
๐Ÿงช Production Department – Diploma / B.Sc / M.Sc Chemistry (2–5 Years) | 50 Positions Role: Shift Operator / Production Executive Qualification: Diploma Chemical / B.Sc / M.Sc Chemistry Experience: 2–5 years   Key Responsibilities Field operation of reactors, centrifuge, pumps, dryers Charging, sampling, filtration & packing activities Follow SOP, GMP & safety practices Maintain shift documentation Report abnormalities ...
5 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
Qualification & Experience M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline 3–5 years of experience in R&D (DQA) Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211 Experience with dermatology products or medical devices is an advantage Key Responsibilities Review development documents, analytical methods, R&D trials, lab notes, PDR, MFR, and batch ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities Production Documentation Prepare, review, and issue Batch Manufacturing Records (BMR) and Batch Production Records (BPR) Maintain daily production logs, shift reports, and production summaries Ensure timely and accurate documentation of production activities SOP & Record Management Draft, revise, and control Standard Operating Procedures (SOPs) related to production Maintain document control registers, master lists, and archival ...
1 Opening(s)
18.0 Year(s) To 25.0 Year(s)
30.00 LPA TO 50.00 LPA
๐Ÿ› ๏ธ Key Responsibilities Plant Maintenance & Reliability Lead Mechanical, Electrical & Instrumentation maintenance for all plant equipment Ensure maximum uptime through preventive & predictive maintenance Develop and implement maintenance strategies, SOPs, and schedules Handle breakdown analysis, RCA, and corrective/preventive actions Utilities & Infrastructure Oversee maintenance of Boilers, Compressors, Cooling Towers, DG Sets, HVAC, ETP/STP Ensure uninterrupted availability of ...
1 Opening(s)
0 To 2.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities: Carry out lab-scale synthesis and development of API intermediates & final products Execute process development, optimization, and scale-up support Perform reaction monitoring, purification, and yield improvement Maintain proper documentation as per GLP & data integrity norms Coordinate with Analytical R&D, QA, and Production for tech transfer Ensure compliance with safety, GMP, and regulatory guidelines
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
  Perform routine analysis of raw materials, in-process, and finished products Operate and handle analytical instruments such as HPLC, GC, Karl Fischer, UV, Particle Size Analyzer, etc. Ensure testing as per approved specifications, SOPs, and pharmacopeial requirements Maintain proper documentation, test records, and compliance with GMP/GLP Basic understanding of pharmaceutical formulations and related quality requirements Support ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Looking for candidates with below profile:๏‚ท Heading QC/ QA with exposure to GMP & ISO audit requirements.๏‚ท Coordination between Plant/ QC and R &D in terms of the new developed processes andimproving existing process / quality control.๏‚ท Accountable for the tuning of batch parameters.๏‚ท Responsible for Quality, Training, Customer audits, ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Looking for candidates with below profile:๏‚ท Heading QC/ QA with exposure to GMP & ISO audit requirements.๏‚ท Coordination between Plant/ QC and R &D in terms of the new developed processes andimproving existing process / quality control.๏‚ท Accountable for the tuning of batch parameters.๏‚ท Responsible for Quality, Training, Customer audits, ...

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