Zydus Lifesciences-PRODUCTION EXPERIENCE- Jobs Career Info

Zydus Lifesciences Limited (Formerly known as Cadila Healthcare Limited), a leading Indian Pharmaceutical company is a fully integrated, global healthcare provider. With in-depth domain expertise in the field of healthcare, it has strong capabilities across the spectrum of the pharmaceutical value chain. From formulations to active pharmaceutical ingredients and animal healthcare products to wellness products, Zydus has earned a reputation amongst Indian pharmaceutical companies for providing comprehensive and complete healthcare solutions.

One of the salient features of Zydus is its rich history and lineage. The origin of the company dates all the way back to the 1950s. The company was founded in the year 1952 by Mr. Ramanbhai B. Patel (late), a first-generation entrepreneur and a doyen in the field of Indian Pharmaceuticals.

In 1995, the group was restructured and thus was formed Cadila Healthcare under the aegis of the Zydus group. From a humble turnover Rs. 250 crores in 1995 the group witnessed a significant financial growth and registered a turnover of over Rs. 17,000 crores in FY-21.

Adhering to its brand promise of being dedicated to life in all its dimensions, Zydus continues to innovate with an unswerving focus to address the unmet healthcare needs. Simultaneously it rededicates itself to its mission of creating healthier, happier communities across the globe.

From 2 to 7 year(s) of experience

₹ 3-7 Lacs P.A.

Ankleshwar

Time and Venue

1st May, 1.00 PM – 3.00 PM

Zydus Lifesciences Limited API Manufacturing, Ankleshwar (Unit-1), Plot No. 291, G.I.D.C Industrial Estate, Ankleshwar-393 002, District: Bharuch, State: Gujarat – INDIA (view on Map)

Job Description

Responsible for overall production planning and execution.
Handling of Plant manpower according to production Planning.
Handling of SAP function.
Management of Raw material in accordance with production Planning.
Co-ordination with cross functional department for production requirements.
Planning and execution of on-time requests for materials for production.
Preparation, review of documents & ensuring that the documents are approved by QA ensuring the instructions are followed for the production of intermediates or API according to written procedures.
Producing APIs and subsequent intermediates according to pre-approved instructions.
Reviewing all production batch records and ensuring that these are completed and signed.
Maintain & verify the production facilities are clean and appropriately disinfected.
Verify that the necessary calibrations are performed and records kept (Wherever applicable)
Preparation of Validation Protocol and reports and verify that the validation protocols and reports are reviewed and approved.
Initiation of change controls and Evaluating proposed changes in product, process or equipment and carrying out risk analysis whenever applicable.
Involve in Qualification of new or modified facilities and equipments.
Maintain & Verify that the Safety procedure are updated and followed.
Reporting of incident, deviation ,failure and involve in investigation