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

Deputy Manager

Location: Ankleshwar
Workplace: On-site

About this role

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.

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