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 & ADL, Process Development, and Technology Transfer on 20th August 2017 for Cadila Healthcare Ltd, API Dabhasa, Gujarat.
Here is a chance to join Zydus at our API Manufacturing located at Dabhasa as.
Job Description:
Experience : 2 to 6 years API Pharma Candidates only
Manufacturing.
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.
PRODUCTION : 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.
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.
Candidates should be M Sc with 2-7 years of experience.
- Relevant exposure in API Process Development of synthesis work.
- Relevant exposure in process development analytical support. Hands on experience of HPLC, GC, Dissolutions apparatus, UV-Visible spectrometer and stability studies in API / Bulk drug production.
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.
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 – 20th August 2017 (Sunday)
- Time of Interview – 09:30 AM to 05:00 PM
- Venue of Interview – Hotel Amar Vilas
Chandra Nagar, A B Road
Indore 452001
