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.…
Monitor critical production KPIs such as batch cycle time, yield, OEE, right-first-time, and schedule adherence. Lead root cause analysis and implementation of corrective and preventive actions. People Leadership Ensure …
Skills: Production Monitoring, Root Cause Analysis, People Leadership, cGMP Compliance, Regulatory 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
Execute batch manufacturing activities as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monitor API manufacturing processes, including reaction, filtration, centrifugation, dryi…
Skills: Batch Manufacturing, API Manufacturing, cGMP, GDP, Data Integrity
Plan and execute daily, weekly, and monthly API production activities as per the production schedule. Ensure adherence to cGMP, SOPs, BMR/BPR, and regulatory requirements. Monitor manufacturing processes, batch yields, c…
Skills: API Production, cGMP Compliance, Production Planning, Team Supervision, CAPA Implementation
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
Lead and maintain the site Quality Management System in compliance with cGMP, ICH, WHO, USFDA, EU GMP, and other applicable regulatory requirements. Review and approve SOPs, specifications, protocols, reports, and qualit…
Skills: Quality Management System, cGMP, ICH Guidelines, WHO Guidelines, USFDA Compliance
Monitor shop floor activities to ensure compliance with cGMP, SOPs, approved Batch Manufacturing Records (BMR), and regulatory requirements. Review Batch Manufacturing Records (BMR), logbooks, equipment records, and GMP …
Skills: cGMP Compliance, Batch Manufacturing Record Review, CAPA Implementation, Quality Risk Management, Process Validation
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
Manage receipt, storage, preservation, and issuance of engineering spare parts and consumables. Maintain inventory of mechanical, electrical, instrumentation, utility, HVAC, and maintenance materials. Ensure timely issua…
Skills: Inventory Management, SAP, ERP, Material Planning, Stock Reconciliation
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
Ensure accurate and timely completion of: Batch Manufacturing Records (BMR) Equipment Logbooks Cleaning Records Calibration Records Usage Logs Shift Reports Maintain compliance with cGMP, GDP, Data Integrity, SOPs, and r…
Skills: Batch Manufacturing Records, cGMP, GDP, Data Integrity, SOP 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, Safety Management, Equipment Calibration
External Job Description JD for Shift Lead – Engineering (Mechanical/Electircal) Attending line breakdowns to maintain efficiency. Manpower handling and leave management. Executing the Preventive & predictive maintenance…
External Job Description Job profile of Executive- I (Production) Desired candidate profile – Bsc. (Chemistry) / M.Sc. (Chemistry) Key Performance Indicator- 1) Ensure adherence to Production process as per laid down pro…
Skills: Production Planning, SAP, Team Supervision, Shopfloor Management, Process Adherence
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 …
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
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
Posted 10d ago
~40 hrs/week
Responsibilities
Responsible for executing preventive and breakdown maintenance of plant equipment to minimize downtime. Ensures strict adherence to safety protocols and maintains comprehensive regulatory documentation for USFDA and ISO audits.
Requirements
Requires the ability to manage technical maintenance checklists and coordinate with Production and QA departments. Must be proficient in cGMP standards and regulatory compliance documentation.
Full job description
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.E (Instrument Measuring Testing Equipment’s) as per direction of Head...
Breakdown Maintenance
Minimize the breakdown time of equipment or system by,
Attending the breakdown as early as possible after receiving the job card. (Intimation of breakdown).
Evaluate the reasons behind the breakdown and find out he appropriate remedies.
Take instructions from Executives and execute them.
Fulfill the safety requirement permission from plant.
After completion of job, ensure that the place is neat and clean.
Energy Conservation
Continues co-ordination with Plant people for minimizing the energy losses by creating awareness of the losses.
Safety
Check the interlocks of systems.
Ensure that all jobs are done by issuing right safety permit and after completions of job it shall properly closed.
Inter departmental co ordination
Any modification in existing system shall co-ordinate with Production & QA department.
Coordination for availability of spares and inform to superior.
Documentation
To prepare USFDA, all regulatory audits, ISO 9001 & ISO 14001 system documentation with proper record.
To prepare of cGMP documentation & proper record of the same.
To ensure compliance regulatory documents & proper record of the same.
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 Engineering jobs are open in Ankleshwar, India right now?
There are currently 141 open engineering positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Engineering 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.
How do I apply for Engineering jobs in Ankleshwar, India?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.