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…
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…
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
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
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
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
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, Equipment Operation, cGMP Compliance, Good Documentation Practices, Process Monitoring
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
• To prepare Technical Comparison & forward to purchase for recommendation • Coordination with consultants for planning & designing. • To ensure the raising of indents in SAP as per design in electrical in time. • To ens…
• Review of analytical data of scale up and validation batches, commercial batches of finished products and also of raw materials, packing material, in process, intermediate, hold time study, stability study and working …
Skills: Analytical Data Review, Regulatory Compliance, SAP, LIMS, Data Integrity
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
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
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
• 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
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…
Preventive Maintenance : • Preventive maintenance of the equipment’s is as per checklist and instruction / Feedback from Section -Incharge. • Prepare preventive Maintenance Checklist for all the plant. • Check the I.M.T.…
• Directly responsible for smooth operation and maintenance of chilled water plant, chilled brine plant, air compressors, cooling tower, purified water plants, soft water plants, filter water plants, pump house and row w…
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
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
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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Full-time
Posted 3d ago
~40 hrs/week
Responsibilities
Supervise production batch charging and monitoring while ensuring strict adherence to SOPs and cGMP standards. Coordinate with QA, QC, and Engineering departments to ensure product quality, timely dispatch, and facility maintenance.
Requirements
Requires the ability to lead workmen, manage online documentation, and maintain high safety and housekeeping standards in a powder processing area. Must be capable of conducting audits and providing safety and quality training to operators.
Full job description
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 plan.
To ensure that proper gowning procedure is followed as per SOP.
To maintain environment condition in PP area as per SOP.
To ensure that there is no contamination in Products.
To ensure that materials are properly labeled.
To ensure and arrange packing materials as per dispatch plan.
To coordination with QC, QA & SCM for sampling and packing.
To hand over the materials to FG stores & to ensure on time dispatches.
To ensure that proper packing procedure is followed and quantities are correct to avoid customer complains.
To coordinate with micro lab for various samplings.
To review completed documents.
To coordinate with engineering any PP area related issues.
To ensure healthiness of AHU system, water system etc.
To ensure that only authorized persons enter in PP area.
To maintain reconciliation of accessories in PP area.
cGMP :
To ensure Intermediates / FP produced is as per quality specification.
To guide / train workmen / trainees in Finished Powder Processing Section
To ensure very high standards of housekeeping in plants and FP areas.
Ensure BPRs of ongoing batches are available at specified places near equipment and are online with production
To ensure tagging of HDPE / Fiber drums, hose pipes etc. used in respective batch processing
To ensure online documentation and submit the compete document to QA department.
To take lead in audit preparednation and comply daily observation of IPQA/QA.
Safety
To ensure safety in PP area.
To educate / train / supervise workmen / in safe handling of chemicals and equipment so as to prevent accidents.
Wastage Avoidance / Reduction
To ensure minimum / no wastage of material.
Training
Train operators on Safety / Quality / wastage reduction.
To ensure that all PP area related trainings are provided to employees.
Inter departmental co-ordination
To coordinate with QA department for Good Document Practice.
To coordinate with Engg. Services for maintenance related work.
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/
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