Ankleshwar, Gujarat, India · On-site
Execute manufacturing operations as per approved Batch Manufacturing Records (BMR), SOPs, and production plans. Supervise shift activities and ensure timely completion of production batches. Handle chemical reactions, cr…
Skills: Manufacturing Operations, BMR Execution, Chemical Reactions, Crystallization, Filtration
Ankleshwar, Gujarat, India · On-site
Perform shop floor QA activities to ensure compliance with cGMP, SOPs, and approved manufacturing procedures. Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), logbooks, and other GMP documents for…
Skills: Quality Assurance, cGMP Compliance, Batch Record Review, Line Clearance, CAPA
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Ankleshwar, Gujarat, India · On-site
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Ankleshwar, Gujarat, India · On-site
Review and approve batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and analytical reports. Perform line clearance activities before and after manufacturing operations. Monitor and verify compl…
Skills: cGMP, GDP, Data Integrity, SOP Review, Line Clearance
Ankleshwar, Gujarat, India · On-site
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Ankleshwar, Gujarat, India · On-site
Monitor shop floor activities to ensure compliance with cGMP, SOPs, approved Batch Manufacturing Records (BMR), and regulatory requirements. Review Batch Manufacturing Records (BMR), logbooks, equipment records, and GMP …
Skills: cGMP Compliance, Batch Manufacturing Record Review, CAPA Implementation, Quality Risk Management, Process Validation
Ankleshwar, Gujarat, India · On-site
Lead and maintain the site Quality Management System in compliance with cGMP, ICH, WHO, USFDA, EU GMP, and other applicable regulatory requirements. Review and approve SOPs, specifications, protocols, reports, and qualit…
Skills: Quality Management System, cGMP, ICH Guidelines, WHO Guidelines, USFDA Compliance
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, finished products, in-process samples, stability samples, and cleaning validation samples. Operate and troubleshoot analytical instruments including HPLC, GC, UV-Visible …
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, KF Titration
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Management, cGMP Compliance, Documentation, Safety Management, Quality Control
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Safety Management, Equipment Calibration
Ankleshwar, Gujarat, India · On-site
Ensure accurate and timely completion of: Batch Manufacturing Records (BMR) Equipment Logbooks Cleaning Records Calibration Records Usage Logs Shift Reports Maintain compliance with cGMP, GDP, Data Integrity, SOPs, and r…
Skills: Batch Manufacturing Records, cGMP, GDP, Data Integrity, SOP Compliance
Ankleshwar, Gujarat, India · On-site
Execute batch manufacturing activities as per approved Batch Manufacturing Record (BMR). Supervise batch charging, reaction monitoring, filtration, centrifugation, drying, milling, blending, and packing operations. Ensur…
Skills: Batch Manufacturing, Reaction Monitoring, Filtration, Centrifugation, Drying
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Safety Management, Equipment Calibration
Ankleshwar, Gujarat, India · On-site
External Job Description Job profile of Executive- I (Production) Desired candidate profile – Bsc. (Chemistry) / M.Sc. (Chemistry) Key Performance Indicator- 1) Ensure adherence to Production process as per laid down pro…
Skills: Production Planning, SAP, Team Supervision, Shopfloor Management, Process Adherence
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, BPR Documentation, Equipment Calibration, Safety Management
Ankleshwar, Gujarat, India · On-site
Production : • Supervision of production & maintenance activities of respective shift. • To ensure that every raw material used is of right quality (approved from QC, having reference Number) and quantity (verifying the …
Skills: Production Supervision, Maintenance Management, Quality Control, SAP Production Module, cGMP Compliance
Ankleshwar, Gujarat, India · On-site
Job Title: Executive – Production, Pharma Educational Qualification and Experience: M. Pharm / B. Pharm from a reputed university, having 1 to 5 years in pharmaceutical manufacturing (Preferably in Granulation , compress…
Skills: Pharmaceutical Manufacturing, Granulation, Compression, Coating, SAP
Ankleshwar, Gujarat, India · On-site
JOB TITLE- Assistant Manager Quality Control, Pharmaceuticals REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry) or B.Pharm/M.Pharm 8-10 years in chemical & instrumental testin…
Skills: Analytical Ability, Troubleshooting, Coordination, Communication, Problem Solving
Ankleshwar, Gujarat, India · On-site
Production : • Supervision of production & maintenance activities of respective shift. • To ensure that every raw material used is of right quality (approved from QC, having reference Number) and quantity (verifying the …
Skills: Production Supervision, SAP Production Module, cGMP Compliance, BPR Implementation, Quality Control
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Execute and supervise manufacturing operations including chemical reactions and packing according to BMRs and SOPs. Coordinate with cross-functional teams to ensure compliance with cGMP and optimize process yields.
Requires expertise in pharmaceutical manufacturing processes and strict adherence to Good Documentation Practices. Must be able to investigate deviations and implement CAPA in coordination with Quality Assurance.
Execute manufacturing operations as per approved Batch Manufacturing Records (BMR), SOPs, and production plans.
Supervise shift activities and ensure timely completion of production batches.
Handle chemical reactions, crystallization, filtration, drying, milling, blending, and packing activities.
Monitor critical process parameters and ensure compliance with process specifications.
Ensure line clearance, equipment cleaning, and status labeling before batch initiation.
Review and complete BMRs, logbooks, equipment records, and production documentation following Good Documentation Practices (GDP).
Coordinate with QA, QC, Engineering, Warehouse, EHS, and Maintenance for smooth manufacturing operations.
Investigate deviations, incidents, OOS/OOT observations, and implement CAPA in coordination with QA.
Ensure compliance with cGMP, Data Integrity, EHS guidelines, and regulatory requirements.
Optimize process yield, reduce cycle time, minimize solvent consumption, and improve productivity.
Monitor utility consumption and ensure effective utilization of manpower and equipment.
The Care Continues...
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world. Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals. At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry. More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs. Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved. The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals. Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products. The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia. For more information visit: https://www.cadilapharma.com/
Offices: Sarkhej-Dholka Road, Bhat, Ahmedabad, Gujarat 382210, IN · Survey No. 1389, Trasad Road, Dholka, Ahmedabad, Gujarat 387 810, IN · 294, GIDC Estate, Ankleshwar, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN
There are currently 138 open science & research positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Cadila Pharmaceuticals Limited, Zentiva, Asian Paints, among others. Browse the listings above to see every active employer.
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
