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
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 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, Good Documentation Practices, Process Equipment Operation, Line Clearance
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, 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 …
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
Perform shop floor QA activities to ensure compliance with cGMP, SOPs, and approved manufacturing procedures. Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), logbooks, and other GMP documents for…
Skills: Quality Assurance, cGMP Compliance, Batch Record Review, Line Clearance, CAPA
Review and approve batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and analytical reports. Perform line clearance activities before and after manufacturing operations. Monitor and verify compl…
Skills: cGMP, GDP, Data Integrity, SOP Review, Line Clearance
Production : • 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 maintenance to avoid any…
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 : • 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
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.…
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
Safety : • Assist to collect safety information. • Maintain the record of MSDS. • Support for the safety activities to colleagues. • Issue of PPE to plants as per requirement. Maintain the consumption records as per SOP,…
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
Ensure compliance with Environmental Clearance (EC), Consent to Operate (CTO), Consent to Establish (CTE), Hazardous Waste Rules, and all applicable environmental regulations. Lead operations and performance improvement …
Skills: Environmental Compliance, Pollution Control Systems, Process Safety Management, Regulatory Coordination, Waste Management
• To ensure cGMP compliance at manufacturing facility [PR, PR (SRP), Quality units, HR, EHS, ST, EG departments] as well as to ensure the whether they are following the standard procedures. • Responsible to ensure online…
Skills: cGMP Compliance, Data Integrity, Line Clearance, Quality Assurance, CAPA
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
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 : • 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
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Full-time
Posted 8d ago
~40 hrs/week
Responsibilities
Oversee production processes, including raw material verification, batch monitoring, and adherence to BPRs and SOPs. Ensure strict compliance with cGMP standards, safety protocols, and accurate documentation of equipment and process records.
Requirements
The candidate must be capable of supervising plant operators and managing the Finished Powder Processing Section. Proficiency in safety standards, MSDS, and coordination with QC and Engineering departments is required.
Full job description
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 BPRs.
To take instruction from shift Incharge/managers for batch charging / monitoring & follow up.
To report any deviation / discrepancy in plant / process to shift in charge.
To complete given task within stipulated time.
To maintain environment conditions in PP/Intermediate area as per SOP
To maintain reconciliation of accessories used in PP/Intermediate area.
To ensure that there is no any contamination in finished product
To do packing & repacking activities as per requirement
To follow proper entry & gowning procedure in PP/Intermediate area
To perform safe operations of plant equipments and utilities.
Documentation
To complete online BPR, equipment usage record & cleaning records with respect to his shift.
To fill area differential pressure record, centrifuge bags records and any other records related to PP area.
cGMP :
To guide & train workmen in Finished Powder Processing Section.
To ensure that yield & quality of finished product is as per predefined norms.
Packing of finished product is as per SOP.
Responsible for maintaining cleanliness of the equipments and area under his charge
To do proper calibrations of weighing balance, pH meter etc. as per SOP.
To update equipment status boards timely.
To ensure on line completion of equipment usage log.
To maintain proper labeling of HDPE / Fiber drums, hose pipes etc. used in respective batch processing.
To fill online documentation/BPR.
To participate in training to keep himself updated about cGMP, technical and safety standards and update his training records timely.
To maintain intermediate product & cleaning material reconciliation.
Safety
To keep himself aware about MSDS of related materials.
To educate and supervise plant operators in safe handling of chemicals and equipment so as to prevent accidents
To coordinate with EHS for various safety permits.
To use scrubber wherever required to avoid air pollution.
Wastage Avoidance / Reduction
To ensure no spillage of solvents & wastage of material.
To close the valves of utilities supplies when not required.
Inter departmental co-ordination
To coordinate with QC department for getting analysis report.
To coordinate with Engg Service for maintenance related work in his shift.
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 Security & Safety jobs are open in Ankleshwar, India right now?
There are currently 69 open security & safety positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Security & Safety roles in Ankleshwar, India?
Companies currently hiring include Cadila Pharmaceuticals Limited, Asian Paints, Indorama Ventures: Indovinya, among others. Browse the listings above to see every active employer.
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