Ensure compliance with cGMP, GDP, GLP, Data Integrity (ALCOA+), SOPs, and regulatory guidelines. Perform shop floor QA activities, including line clearance, equipment clearance, area clearance, and in-process verificatio…
Skills: cGMP, GDP, GLP, Data Integrity, Quality Assurance
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
Monitor and maintain PLC, SCADA, and DCS-based process control systems. Diagnose and rectify control system failures in coordination with automation and production teams. Support modification, optimization, and commissio…
Skills: PLC, SCADA, DCS, Process Control Systems, Automation Systems
Handle mechanical engineering activities for API manufacturing plants and utilities. Review equipment specifications, datasheets, GA drawings, P&IDs, and technical documents. Support installation, commissioning, qualific…
Skills: Mechanical Engineering, Equipment Maintenance, SAP PM, SAP MM, GMP Compliance
Principal Tasks &Responsibilities Maintenance Services : • To distribute the daily work to technician as per plant & Utility job request & ensure timely compliance. • To co-ordinate with electrical, instrument and Utilit…
• Logging, review of Market complaints and fulfilments of other market requirements. • Logging, review of Return Goods and product recall. • Regulatory Compliances. • Responsible for customer audit and its responses. • R…
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, blending, and packing. …
Skills: API Manufacturing, Batch Manufacturing Records, SOP Compliance, Unit Operations, cGMP
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
Principal task and responsibilities: Support in Master Data Management and Training to employees. To perform the CSV related to computerized systems across the sites &its compliance. IT Compliance for computerized system…
Skills: Master Data Management, CSV, IT Compliance, GMP, Change Control
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, Batch Processing, SAP
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
• 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
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
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, Quality Control, BPR Documentation
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…
Execute API manufacturing operations such as charging, reaction monitoring, filtration, centrifugation, drying, blending, milling, and packing as per approved BMRs and SOPs. Ensure timely completion of production activit…
Skills: API Manufacturing, BMR Documentation, SOP Compliance, cGMP, Reaction Monitoring
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
• 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
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, blending, and packing. …
Skills: API Manufacturing, Batch Manufacturing Records, SOP Compliance, Unit Operations, cGMP
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Full-time
Posted 8h ago
~40 hrs/week
Responsibilities
Operate and monitor Effluent Treatment Plant (ETP) systems and associated utilities to ensure compliance with environmental discharge norms. Coordinate with cross-functional teams for waste management, equipment maintenance, and process optimization.
Requirements
The role requires technical proficiency in monitoring process parameters like pH, COD, and BOD, alongside experience in maintaining industrial equipment. Candidates must be capable of managing chemical inventories and ensuring adherence to EHS and regulatory standards.
Full job description
Operate and monitor ETP systems, including collection tanks, neutralization units, aeration systems, clarifiers, filter presses, RO systems, MEE, ATFD, and associated utilities. Ensure effective treatment of effluents to achieve compliance with prescribed discharge norms and environmental regulations. Monitor key process parameters such as pH, COD, BOD, TDS, TSS, flow rate, dissolved oxygen, and chemical dosing. Coordinate with Production, Utilities, and EHS teams for the segregation, collection, and treatment of various effluent streams. Maintain daily operational logs, shift reports, checklists, and statutory records related to ETP operations. Conduct routine inspections of pumps, blowers, agitators, pipelines, dosing systems, and other ETP equipment. Coordinate preventive maintenance, breakdown maintenance, and calibration activities with the Engineering team. Ensure proper handling, storage, and disposal of ETP sludge and hazardous waste in accordance with regulatory requirements. Monitor chemical consumption and maintain optimum inventory levels of treatment chemicals and consumables. Support environmental monitoring activities, including wastewater sampling and analysis. Ensure compliance with EHS guidelines, permit conditions, and emergency response procedures. Participate in internal audits, environmental audits, customer audits, and regulatory inspections. Identify opportunities for process optimization, water conservation, waste minimization, and cost reduction.
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/
How many Manufacturing jobs are open in Ankleshwar, India right now?
There are currently 165 open manufacturing positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Ankleshwar, India?
Companies currently hiring include Cadila Pharmaceuticals Limited, Zentiva, Asian Paints, Indorama Ventures: Indovinya, among others. Browse the listings above to see every active employer.
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