Home / B.Pharm / Walk-In for Production / Quality Control / Assurance / R&D Process @ Zydus Cadila

Walk-In for Production / Quality Control / Assurance / R&D Process @ Zydus Cadila

Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted revenues of over Rs. 8600 crores in FY15. The group had posted a turnover of Rs. 4600 crores in FY 11, making it a billion dollar company. Recently, the group launched Exemptia, the world’s first biosimilar for Adalimumab, the largest selling therapy worldwide for inflammatory arthritis.

Walk-in for Production, Quality Control , Quality Assurance & 

R & D Department  Process `Development , Technology Transfer on 05th August 2017 at Cadila Healthcare Ltd, API Dabhasa Multi Product Plant

Here is a chance to join Zydus at our API Manufacturing located at Dabhasa as.

Job Description:

Qualification: M.Sc / B.Sc, B.E , Diploma Chemical (Chemistry / Chemical)

Experience : 2 to 6 years API Pharma Candidates only

Designation : Executive / Sr.Executive / Assistant Manager

Key Responsibilities are mentioned as below:
QUALITY CONTROL : Candidate should have hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab, micro lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.
QUALITY ASSURANCE : Candidate must be familiar with cGMP requirements, Data Integrity, Document Cell, Batch release process, Trending APR shop floor Operation in API / Bulk Drug

a) Data Integrity – Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.

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b) Document Cell -Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.

c) Batch Release – Knowledge of ICH guidelines and should review of BMRs and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.

d) Technology transfer documents – Review R&D process & TTD, evaluation of CPP & CQA and comparison with batch record , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.

e) Trending and APR – Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, validation Protocols and reports and Annual Review reports.

 :Candidate should have experience and relevant exposure in API / Bulk Drug Manufacturing. Should also have knowledge of GMP documentation. Must be familiar with cGMP requirements.

Analytical Development : M Sc / Ph D with 2 7 yrs relevant experience. Exposure in Method Development , Method Validation, Handling HPLC, UPLC, LC-MS, XRD, GC, Calibration & trouble Shooting.

Research & Development : M Sc / Ph D with 2-7 yrs in API Process Development. Experience in handling multistage reactions with knowledge of analytical data interpretation; literature search, non-infringing route of synthesis and in depth knowledge of organic chemistry.

Process Development (API) Scientific Assistant / Sr Scientific Assistant / Research Associate / Sr Research Associate
Candidates should be M Sc with 2 8 years of experience and relevant exposure in API Process Development of synthesis work.

Technology Transfer : B E (Chemical) with 2 5 yrs relevant experience. Experience in Scale-up activities, Plant capacity optimization by debottlenecking, working in kilo lab. Preparation & review of PFD & P&ID. Preparation and review of equipment specification. Commissioning activities for modification or changes in existing as well as new projects.

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Candidate should possesses excellent communication & interpersonal skills. Hands on exposure with software like SAP, LIMS, MS Office etc.

Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.

Desired Profile:

  • UG -B.Sc – Chemistry
  • PG – MS/M.Sc(Science) – Chemistry

Walk-In Details:

  • Date of Interview – 05th August 2017 (Saturday)
  • Time of Interview – 09:30 AM to 04:00 PM
  • Venue of Interview – Hotel Shalimar, Valia Road, Near G.I.D.C. Reservoir, Ankleshwar, Dist : Bharuch Gujarat 393002

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