Cadila Pharmaceuticals Limited

Pharmaceutical Manufacturing5,001-10,000 employees peopleFounded 1951On-site

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/

Location

Ankleshwar, Gujarat, India

View company cadilapharma.com LinkedIn

Technical Supervisor

Location: Ankleshwar
Workplace: On-site

About this role

Production

To take instruction from plant-in-charge for batch charging / monitoring
To report any deviation / discrepancy in plant / process to plant in charge
To ensure completion of batches as per production plan.
To ensure that proper gowning procedure is followed as per SOP.
To maintain environment condition in PP area as per SOP.
To ensure that there is no contamination in Products.
To ensure that materials are properly labeled.
To ensure and arrange packing materials as per dispatch plan.
To coordination with QC, QA & SCM for sampling and packing.
To hand over the materials to FG stores & to ensure on time dispatches.
To ensure that proper packing procedure is followed and quantities are correct to avoid customer complains.
To coordinate with micro lab for various samplings.
To review completed documents.
To coordinate with engineering any PP area related issues.
To ensure healthiness of AHU system, water system etc.
To ensure that only authorized persons enter in PP area.
To maintain reconciliation of accessories in PP area.

cGMP :

To ensure Intermediates / FP produced is as per quality specification.
To guide / train workmen / trainees in Finished Powder Processing Section
To ensure very high standards of housekeeping in plants and FP areas.
Ensure BPRs of ongoing batches are available at specified places near equipment and are online with production
To ensure tagging of HDPE / Fiber drums, hose pipes etc. used in respective batch processing
To ensure online documentation and submit the compete document to QA department.
To take lead in audit preparednation and comply daily observation of IPQA/QA.

Safety

To ensure safety in PP area.
To educate / train / supervise workmen / in safe handling of chemicals and equipment so as to prevent accidents.

Wastage Avoidance / Reduction

To ensure minimum / no wastage of material.

Training

Train operators on Safety / Quality / wastage reduction.
To ensure that all PP area related trainings are provided to employees.

Inter departmental co-ordination

To coordinate with QA department for Good Document Practice.
To coordinate with Engg. Services for maintenance related work.

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