Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, finished products, in-process samples, solvents, and stability samples as per approved specifications and SOPs. Operate analytical instruments such as HPLC, GC, UV-Visibl…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Dissolution Testing
Ankleshwar, Gujarat, India · On-site
Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, dryers, filters, blenders, and other process equipment. En…
Skills: Batch Manufacturing, cGMP, EHS, Data Integrity, Equipment Operation
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure compliance with cGMP,…
Skills: API Manufacturing, cGMP, GDP, EHS, Data Integrity
Ankleshwar, Gujarat, India · On-site
Perform and review analysis of raw materials, intermediates, finished products, in-process, stability, water, and cleaning validation samples as per approved specifications and test methods. Operate, troubleshoot, and ma…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Karl Fischer Titration
Ankleshwar, Gujarat, India · On-site
JOB TITLE Assistant Manager- Quality Control, Chemistry REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry ) 8 to 10 years in chemical & instrumental testing laboratory with exp…
Skills: Quality Control, Organic Chemistry, Analytical Chemistry, GMP, GLP
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, finished products, in-process samples, and stability samples as per approved specifications and test methods. Operate and maintain analytical instruments such as HPLC, GC…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Dissolution Testing
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
Perform chemical analysis of raw materials, intermediates, APIs, stability samples, and finished products using approved analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Visible Spectr…
Skills: Chemical Analysis, HPLC, GC, UV-Visible Spectrophotometry, FTIR
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
• 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
Documentation: • To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. • Ensure that all documents / records required for Regulatory Compliance are main…
Skills: SOP Preparation, Regulatory Compliance, GDP, GMP Compliance, CAPA
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and approved Standard Operating Procedures (SOPs). Operate and monitor reactors, centrifuges, dryers, filters, blenders, micronizers, and othe…
Skills: API Manufacturing, cGMP, GDP, Data Integrity, Equipment Operation
Ankleshwar, Gujarat, India · On-site
Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monitor process equipment …
Skills: API Manufacturing, cGMP, Good Documentation Practices, Process Equipment Operation, Line Clearance
Ankleshwar, Gujarat, India · On-site
Process Development: • Conduct laboratory experiments & trials to modify processes develop shorter processes to reduce present cost. • Send sample to QC of studied experiment. • Contact QC dept. to solicit support & foll…
Skills: Process Development, Laboratory Experiments, Sample Analysis, Data Generation, Vendor Qualification
Ankleshwar, Gujarat, India · On-site
Participate in customer, regulatory, and internal audits including USFDA, MHRA, WHO-GMP, EDQM, and other global regulatory inspections. Provide analytical data and laboratory documentation during inspections. Ensure audi…
Skills: Regulatory Audits, Analytical Documentation, cGMP, GLP, Data Integrity
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
Execute API manufacturing batches as per Batch Manufacturing Records (BMR), SOPs, and approved process parameters. Independently handle shift production activities including charging, reaction monitoring, filtration, cen…
Skills: API Manufacturing, Batch Manufacturing Records, cGMP, GDP, Data Integrity
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
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Perform analysis of raw materials, intermediates, and finished products using various analytical instruments according to SOPs. Maintain laboratory equipment, record data in LIMS, and ensure compliance with GLP and GMP standards.
Experience operating analytical laboratory equipment and conducting stability studies is required. Knowledge of ALCOA+ principles, data integrity, and regulatory compliance is essential.
Perform analysis of raw materials, intermediates, finished products, in-process samples, solvents, and stability samples as per approved specifications and SOPs.
Operate analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Tester, Karl Fischer, pH Meter, TOC Analyzer, and other laboratory equipment.
Prepare analytical solutions, mobile phases, reagents, standards, and volumetric solutions as per SOPs.
Conduct calibration, verification, and routine maintenance of laboratory instruments.
Ensure accurate recording of analytical data in laboratory notebooks, worksheets, logbooks, and LIMS where applicable.
Review analytical results and report any Out of Specification (OOS), Out of Trend (OOT), or abnormal observations immediately.
Perform sampling of raw materials, packaging materials, water, utilities, and finished products as per approved procedures.
Support method verification, method transfer, and analytical method validation activities.
Participate in stability studies and environmental monitoring activities as assigned.
Ensure compliance with ALCOA+ principles and Data Integrity requirements.
Maintain laboratory housekeeping and ensure compliance with Good Laboratory Practices (GLP).
Follow Good Manufacturing Practices (GMP), safety guidelines, and regulatory requirements.
Assist during customer, regulatory, and internal audits by providing required documentation and analytical records.
Coordinate with QA, Production, Warehouse, and Engineering departments for timely sample testing and release.
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
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