About Intas :
The firm is one of the integrated Company having relations with top MNC's delivering them high class medicine and pesticides. The company is equipped with around 8000 employees with 2400 in North America and ~1100 in R&D. It is having its footprints in USA, India, Europe, North America and china. while connected to the top MNC's this is delivering the products with quality and competitive prices. The company have sales in about 100 countries.
The Portfolios of the firm include Solid Dosage Formulations, APIs, Radio pharmaceuticals, Advance Intermediates, Fine Ingredients, Allergy Therapy Products, Life Science Chemicals, Crop Science Ingredients and Nutritional Products.
Intas is having a strong expertise in chemistry and in bio-sciences, and is continuously improving its values and strategies to deliver the ultimate outputs. The efforts of this are reported from 2003. The company having the strengths of Strong R&D team and facilities, non infringement process for product development. The company having the title of "Partner of Choice" for the TOP MNC's.
About the Job :
Date of Walk-in : 4th Sep 22
Time : 09 : 30 to 05:00 am
Venue : Baroda productivity council, Productivity House, BPC Road, Alkapuri, Vadodara - 390007
email : [email protected]
Experience : 2-7 years
Qualification : MSc / B. Pharma / M. Pharma
Department : QA (IPQA , Equipment qualification , Documentation
JD :
Required experience in IPQA, documentation, equipment qualification in solid orals and injectable facility
Packing and Manufacturing Officer / Executive
Qualification : B. Pharma or M. Pharma
Experience : 2-7 years
Required experience in Granulation / compression, coating activities and for packing : Experience in primary and secondary line activities required.
Experience in Batch manufacturing, aseptic area Lyo, autoclave supervision and documentation activities. Required to have experience with parenteral packing and documentation activities
For QC
Qualification : M. Pharma or B. Pharma or MSc
Experience : 2-7 years
JD :
Experience in Operating the HPLC, GC and experience with method validation / transfer is required
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