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
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
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
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
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
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
MISSION STATEMENT The Senior API Procurement Category Manager is the strategic commercial owner of Zentiva’s assigned Indian supplier portfolio for Active Pharmaceutical Ingredients (APIs) and Key Starting Materials (KSM…
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
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…
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 …
External Job Description Gate Entry and Inwarding of materials against PO, Invoice and relevant documents Coordinate with Transporters, Buyers and Suppliers was resolving issues, disputes and discrepancy. Ensure 100% com…
Skills: SAP-MM, EWM, MS Excel, MS PowerPoint, Power BI
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Full-time
Posted 10d ago
~40 hrs/week
Responsibilities
Responsible for overseeing production processes, maintaining batch records, and ensuring cGMP compliance in the powder processing area. The role involves monitoring plant equipment, managing raw materials, and coordinating with QC and Engineering departments.
Requirements
Requires the ability to perform safe plant operations, maintain detailed technical documentation, and supervise workmen. Must be proficient in following SOPs and maintaining safety standards such as MSDS and EHS permits.
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 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.
How do I apply for Manufacturing jobs in Ankleshwar, India?
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