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, BPR Documentation, Plant Operations, Safety Supervision
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 raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11 compliance by followin…
Skills: GLP, GMP, Wet Analysis, CFR 21 Part 11, LIMS
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, SAP Production Module, cGMP Compliance, Quality Control
Ankleshwar, Gujarat, India · On-site
• To ensure the timely sampling and testing of purified water, Process and finish product samples. • To ensure timely regeneration and maintenance of the Culture • To ensure the media preparation as per the analysis plan…
Skills: Microbiology Testing, Environmental Monitoring, LIMS, GLP, GMP
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, Plant Equipment Operation, Safety Management
Ankleshwar, Gujarat, India · On-site
Participate in investigations related to OOS, OOT, deviations, incidents, and CAPA implementation. Support method validation, method transfer, cleaning validation, and stability studies. Assist during internal audits, cu…
Skills: Investigations, CAPA Implementation, Method Validation, Method Transfer, Cleaning Validation
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, Plant Operations, Safety Management
Ankleshwar, Gujarat, India · On-site
Perform routine analysis of raw materials, intermediates, finished products, stability samples, and cleaning validation samples. Operate and maintain analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer,…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Karl Fischer
Ankleshwar, Gujarat, India · On-site
erform analysis of raw materials, packing materials, in-process samples, intermediates, finished products, stability samples, and utilities as per approved specifications and test methods. Operate and maintain analytical…
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 Monitoring, cGMP Compliance, Documentation, Plant Operations, Safety Management
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 Compliance, Good Documentation Practices, Process Equipment Operation, Line Clearance
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, SAP
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/intermediates…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
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
Principal task and responsibilities : • To verify raw material/ packing materials as per BPR/documents at work place with coordination of warehouse. • To coordinate with engineering departments for breakdown & preventive…
Skills: SAP Production Module, cGMP Compliance, Batch Production Records, Equipment Calibration, Process Validation
Ankleshwar, Gujarat, India · On-site
Production : • To take instruction from plant-in-charge for batch charging / monitoring • To report any deviation / discrepancy in plant / process to plant in charge • To ensure completion of batches as per production pl…
Skills: Production Monitoring, cGMP Compliance, Batch Processing, Quality Assurance, Safety Supervision
Ankleshwar, Gujarat, India · On-site
Execute solvent recovery operations through distillation, rectification, filtration, evaporation, and storage systems as per approved SOPs and process parameters. Operate and monitor SRP equipment, including distillation…
Skills: Solvent Recovery, Distillation, Rectification, Filtration, Evaporation
Ankleshwar, Gujarat, India · On-site
Production : • To receive crude solvents from plants and issue recovered solvents to plants. • To check the labels of raw material, packing materials and solvents before usage. • Perform column distillation as per SDR. •…
Skills: Column Distillation, cGMP, Plant Operations, Chemical Handling, SOP Compliance
Ankleshwar, Gujarat, India · On-site
Review Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), logbooks, and other GMP documents for completeness, accuracy, and compliance. Ensure timely review and disposition of manufacturing records to supp…
Skills: BMR Review, BPR Review, GMP Compliance, Documentation Audit, Material Reconciliation
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Oversee production processes, including raw material verification, batch monitoring, and adherence to BPRs and SOPs. Ensure strict cGMP compliance, maintain equipment cleanliness, and supervise plant operators for safe chemical handling.
Requires expertise in pharmaceutical production, documentation, and safety standards. Must be able to coordinate between QC and Engineering departments while managing plant utilities and environmental conditions.
cGMP :
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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