Science & Research Jobs in Ankleshwar, India (Now Hiring) — 139 open

Cadila Pharmaceuticals Limited

Senior Executive

Ankleshwar, Gujarat, India · On-site

Senior

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

Cadila Pharmaceuticals Limited

Junior Officer

Ankleshwar, Gujarat, India · On-site

Entry level

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

Cadila Pharmaceuticals Limited

Senior Executive

Ankleshwar, Gujarat, India · On-site

Senior

• 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

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, blending, and packing. …

Skills: API Manufacturing, Batch Manufacturing Records, SOP Compliance, Unit Operations, cGMP

Cadila Pharmaceuticals Limited

Executive

Ankleshwar, Gujarat, India · On-site

Mid level

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, SAP Production Module, cGMP Compliance, Quality Control, BPR Documentation

Cadila Pharmaceuticals Limited

Senior Executive

Ankleshwar, Gujarat, India · On-site

Senior

• 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

Cadila Pharmaceuticals Limited

Deputy Manager

Ankleshwar, Gujarat, India · On-site

Senior

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: Regulatory Compliance, SOP Preparation, Documentation Management, Audit Preparedness, GMP Compliance

Cadila Pharmaceuticals Limited

Assistant Manager

Ankleshwar, Gujarat, India · On-site

Mid level

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

Cadila Pharmaceuticals Limited

Senior Officer

Ankleshwar, Gujarat, India · On-site

Mid level

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

Cadila Pharmaceuticals Limited

Executive

Ankleshwar, Gujarat, India · On-site

Mid level

• 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, CFR 21 Part-11, Laboratory Analysis, Instrument Calibration

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

Execute API manufacturing operations such as charging, reaction monitoring, filtration, centrifugation, drying, blending, milling, and packing as per approved BMRs and SOPs. Ensure timely completion of production activit…

Skills: API Manufacturing, BMR Documentation, SOP Compliance, cGMP, Reaction Monitoring

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, blending, and packing. …

Skills: API Manufacturing, Batch Manufacturing Records, SOP Compliance, Unit Operations, cGMP

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

• 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

Cadila Pharmaceuticals Limited

Senior Officer

Ankleshwar, Gujarat, India · On-site

Mid level

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

Cadila Pharmaceuticals Limited

Junior Officer

Ankleshwar, Gujarat, India · On-site

Entry level

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

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

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

Cadila Pharmaceuticals Limited

Senior Officer

Ankleshwar, Gujarat, India · On-site

Mid level

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

Cadila Pharmaceuticals Limited

Senior Executive

Ankleshwar, Gujarat, India · On-site

Senior

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, BPR Documentation, Plant Operations, Safety Supervision

Cadila Pharmaceuticals Limited

Senior Officer

Ankleshwar, Gujarat, India · On-site

Senior

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

Cadila Pharmaceuticals Limited

Officer

Ankleshwar, Gujarat, India · On-site

Mid level

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

Senior Executive

Cadila Pharmaceuticals Limited

Ankleshwar, Gujarat, India • On-site

Senior

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Full-time
Posted 1d ago
~40 hrs/week

Responsibilities

Supervise production and maintenance activities to ensure batch completion according to BPRs and quality specifications. Manage plant equipment utilization, safety compliance, and inter-departmental coordination with QA, QC, and EHS.

Requirements

Requires expertise in production supervision, SAP transactions, and strict adherence to cGMP and safety standards. Must be capable of training staff and managing documentation for chemical processing.

Full job description

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 weights, if required by re weighing) in every batch
To ensure 100% implementation of process conditions for batch as per BPRs.
To take instruction from managers for batch charging / monitoring & to execute.
To ensure maximum utilization of plant equipment & manpower in respective shift
To report any deviation / discrepancy in plant / process to his to reporting manager.
To ensure completion of batches as per plan.
To do SAP transaction related to production module.

Documentation

To ensure to have online completion documents with respect to his shift.
To check critical operation with respect to BPR and to verify the related document.

Quality

To ensure that instructions in BPRs are followed judiciously
To ensure Intermediates / FP produced is as per quality specification
To guide / train workmen / trainees / contract workmen in Finished Powder Processing Section.
To ensure very high standards of housekeeping in plants and FP areas.

cGMP :

To ensure proper calibrations of pH meters & weighing balance as per SOP.
To ensure timely updation of equipment status board
Ensure BPRs of ongoing batches are available at specified places near equipment and are online with production
To ensure on line completion of equipment usage log & documentation.
To ensure labeling of HDPE / Fiber drums, hose pipes etc. used in respective batch processing.

Safety

To ensure awareness to MSDS
To educate / train / supervise workmen / Trainees / contract workmen in safe handling of chemicals and equipment so as to prevent accidents
To ensure the operators are aware / trained in usage of PPE
To coordinate with EHS for various safety permits

Wastage Avoidance / Reduction

To ensure no spillage of solvents & wastage of material.
To ensure closing of valves for utilities supplies when not required (cross check when operation is complete)
Switching of reactor and plant lamps when not required

Training

To train operators & subordinate on Safety / Quality / wastage reduction
To guide / train workmen / trainees in Finished Powder Processing Section.

Inter departmental co-ordination

To coordinate with QA department for Good Document Practice.
To coordinate with QC department for getting analysis report.
To coordinate with Engg Service for maintenance related work.
To coordinate with EHS for safety and environment related issues.
To coordinate with HR for Manpower related issues.

Related keywords

ProductionMaintenanceQCBPRSAPcGMPpH MetersSOPHDPEMSDSPPEEHSFinished Powder ProcessingGood Document PracticeChemical HandlingWaste Reduction

About Cadila Pharmaceuticals Limited

LinkedIn Visit site

The Care Continues...

Industry: Pharmaceutical Manufacturing
Company size: 5,001-10,000 employees
Founded: 1951
Headquarters: Ahmedabad, Gujarat
LinkedIn followers: 623,227

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

Finished FormulationsPre-Clinical/Clinical TrialsAgro productsDiscovery Research ServicesPharma MachineryContract Manufacturinggeneric drugsand bulk drugs / APIsHealth CareBiotechnology

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