• 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…
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
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
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
Position: Assistant Manager – Store (API) Department: Stores & Warehouse Location: API Manufacturing Plant Ankleshwar Reports To: Assistant General Manager – Stores Job Purpose To manage API warehouse operations, ensurin…
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 …
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
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…
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
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
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…
The General Manager – Operational Excellence & Plant Head is responsible for leading the overall operations of the API manufacturing facility while driving continuous improvement initiatives to achieve world-class operat…
Skills: Plant Leadership, Operational Excellence, Lean Manufacturing, Six Sigma, TPM
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…
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To perform the analysis as per work allocation and records the results in …
Maintenance services : • Overall responsible for compliance and maintenance of instrumental equipments/machineries at site. • Ensure preventive maintenance of the equipment’s as per checklist and instruction / Feedback f…
Skills: Preventive Maintenance, Breakdown Maintenance, Instrument Calibration, Troubleshooting, Energy Conservation
• 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…
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
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, Batch Production Records
• Coordination with vendors for quotations & specifications for project. • Coordinate with Purchase team for project related procurement/job matters. • Coordinate with Finance team for payment related matters. • Coordina…
Skills: Vendor Coordination, Procurement, Project Execution, Technical Comparison, SAP
• 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
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Full-time
Posted 3d ago
~40 hrs/week
Responsibilities
Manage the daily operations of the microbiology laboratory, including sampling, testing of purified water and products, and environmental monitoring. Ensure regulatory compliance through proper documentation, instrument validation, and adherence to GMP/GLP standards.
Requirements
The candidate must be able to perform aseptic testing, manage laboratory reagents, and handle OOS incidents. Experience in maintaining laboratory instruments and coordinating with QA and production departments is required.
Full job description
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 planning and the effectiveness and sterility of the media to be ensured.
To ensure the aseptic condition of the microbiology testing area to be maintained
To ensure environment monitoring in the powder processing area and microbiology laboratory. Preparation of the trend for the evaluation of the environment condition of the area.
To ensure maximum utilization of laboratory Instruments.
To ensure the lab preparativeness for the regulatory and customer audits.
To ensure the timely purchase of the media ,cultures and other lab regents
To ensure the effective planning of the daily activity of the microbiology lab.
To ensure the every analysis is to be analysed as per predefined specification and method of analysis.
To report any OOS/incidents / Deviation/ discrepancy in laboratory analysis to section in charge /QC In-charge.
Ensure daily on-line entry in LIMS modules.
Ensure the calibration ,operational and validation status of the instruments in the microbiology laboratory
Ensure the timely Qualification / Validation of all instruments in microbiology laboratory.
Co-ordinate with service engineer regarding break-down and preventive maintenance of instruments.
Ensure that all documents / records required for Regulatory Compliance are maintained properly.
To ensure the analytical documents like specification, protocol, STP, are prepared as per SOP.
Ensure all issues related to completed batches are resolved and documents are transferred to QA.
To maintain instruments logbooks properly as per analysis.
To maintain the GLP and GMP practices & ensure standards procedures in Quality Control laboratory followed effectively.
To ensure the safe disposal of the media and culture waste.
To educate and train the workmen and implement in safe handling of media, reagents, cultures, chemicals, gas cylinder and laboratory instruments to prevent the accidents.
To ensure the storage of lab. Chemicals and test samples at proper place with segregation to prevent accidents.
To coordinate with QA department for cGMP system
To coordinate with production department for planning/clubbing of analysis.
Related keywords
MicrobiologyPurified Water TestingLIMSGMPGLPAseptic ConditionEnvironmental MonitoringOOSDeviationInstrument ValidationSTPSOPRegulatory AuditsQuality ControlMedia PreparationCulture Maintenance
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?
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