Ankleshwar, Gujarat, India · On-site
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
Ankleshwar, Gujarat, India · On-site
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, BMR Execution, cGMP Compliance, Good Documentation Practices, Equipment Operation
Bhat, Jammu and Kashmir, India · On-site
Role & Responsibilities • Having knowledge of S4HANA tools for Annual budget planning, MIS reporting, Finance closing cockpit, Consolidation of financial. statement etc. • Having knowledge of FIORI application. • Having …
Skills: S4HANA, FICO, Financial Closing Cockpit, FIORI, Cost Centre Accounting
Guwahati, Assam, India · On-site
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing f…
Skills: Sales Promotion, Market Strategy Implementation, Market Analysis, Customer Identification, Stockist Management
Patna, Bihar, India · On-site
1. Achievement of Targeted Business Volumes • Achieve overall monthly and annual sales targets for the assigned region. • Deliver brand-wise sales targets with special attention on Focussed & New brands. • Ensure achieve…
Skills: Sales Management, KOL Development, Channel Management, Forecasting, Supply Chain Coordination
Ankleshwar, Gujarat, India · On-site
• Performing all activities related to receipt and issuance of raw material and packing material as per cGMP requirement. • To face customer and regulatory audits. • Unloading of solvents from tanker to respective storag…
Skills: Warehouse Management, cGMP Compliance, Inventory Control, FIFO System, Material Handling
Bhat, Jammu and Kashmir, India · On-site
Role: The MIS & Finance Analytics role is responsible for delivering timely, accurate, and insight-driven financial reports to support business decision-making. The role focuses on transforming data into meaningful analy…
Skills: MIS Reporting, Financial Analytics, Budgeting, Forecasting, Data Governance
Ankleshwar, Gujarat, India · On-site
• 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
Ankleshwar, Gujarat, India · On-site
• 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…
Skills: Regulatory Compliance, Quality Assurance, CAPA, Vendor Qualification, Internal Auditing
Ankleshwar, Gujarat, India · On-site
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
Amritsar, Punjab, India · On-site
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing feedbac…
Skills: Sales Promotion, Market Strategy Implementation, Territory Management, Customer Identification, Stockist Management
Dholka, Madhya Pradesh, India · On-site
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure. • Analysis of Stability Samples as per schedule • To follow s…
Skills: HPLC, UV Spectroscopy, FTIR, cGMP, GLP
Kolkata, West Bengal, India · On-site
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing feedbac…
Skills: Sales Promotion, Market Strategy Implementation, Territory Management, Customer Identification, Stockist Management
Ankleshwar, Gujarat, India · On-site
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
Dholka, Madhya Pradesh, India · On-site
JOB RESPONSIBILITIES To support ISBU through new and renewal dossier submission, pre-registration recommendation response preparation and share with Customer for new and renewal dossier submission, update dossier as per …
Skills: Regulatory Affairs, Dossier Submission, LATAM Market Regulations, Technical Document Review, Compliance
Karnal, Haryana, India · On-site
Major Purpose of the Job: RACI – Matrix – FO is Responsible for Sales & Achieving Budgets Brand Ambassador – Page 3 Personality R – Responsible, A - Accountable, C - Coaching & I - Information Principal Tasks and Respons…
Skills: Sales Achievement, Prescription Generation, Retail Chemist Prescription Audit, Pre-Call Planning, Customer Conversion
Prayagraj, Uttar Pradesh, India · On-site
Principal Tasks and Responsibilities: . Field Work & Sales Achievement Promote company products to the doctors and pharmacists in line with divisional strategies and guidelines. Achieve the assigned sales budget through …
Skills: Sales Achievement, Prescription Generation, Retail Chemist Prescription Audit, Pre-Call Planning, Product Promotion
Ankleshwar, Gujarat, India · On-site
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…
Skills: Solvent Recovery, Distillation, Rectification, Filtration, Evaporation
Varanasi, Uttar Pradesh, India · On-site
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing f…
Skills: Sales Promotion, Market Strategy Implementation, Market Analysis, Customer Identification, Stockist Management
Tikamgarh, Madhya Pradesh, India · On-site
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing feedbac…
Skills: Sales Promotion, Market Strategy Implementation, Territory Management, Customer Identification, Stockist Management
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Execute manufacturing activities for API intermediates and finished products using reactors, centrifuges, and dryers according to BMRs and SOPs. Monitor process parameters, document production activities, and coordinate with QA/QC teams to ensure compliance and quality.
Requires the ability to operate pharmaceutical process equipment and adhere to cGMP and data integrity principles. Must be capable of investigating deviations and supporting process validation and scale-up activities.
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 such as reactors, centrifuges, filters, dryers, micronizers, blenders, and associated utility systems.
Ensure adherence to process parameters, critical process controls, and yield targets during manufacturing operations.
Perform line clearance activities and verify equipment cleanliness before batch initiation.
Monitor and document production activities, including batch records, equipment logbooks, and process checklists.
Coordinate with Quality Assurance and Quality Control teams for in-process sampling, material release, and batch documentation review.
Ensure compliance with cGMP, Good Documentation Practices (GDP), data integrity principles (ALCOA+), and EHS requirements.
Investigate and report deviations, incidents, process abnormalities, and safety concerns; support CAPA implementation.
Coordinate with Warehouse, Engineering, EHS, and Utilities teams to ensure uninterrupted manufacturing operations.
Monitor raw material consumption, process yields, cycle times, and wastage to optimize productivity and reduce costs.
Support technology transfer, process validation, cleaning validation, and scale-up activities.
The Care Continues...
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/
Offices: Sarkhej-Dholka Road, Bhat, Ahmedabad, Gujarat 382210, IN · Survey No. 1389, Trasad Road, Dholka, Ahmedabad, Gujarat 387 810, IN · 294, GIDC Estate, Ankleshwar, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN
The Care Continues...
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/
Offices: Sarkhej-Dholka Road, Bhat, Ahmedabad, Gujarat 382210, IN · Survey No. 1389, Trasad Road, Dholka, Ahmedabad, Gujarat 387 810, IN · 294, GIDC Estate, Ankleshwar, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN
