At Umavida we continuously work hard to deliver affordable and best quality medicines to the needy patient, Umavida Believes in innovation and strives to make a mark in the world of Pharmaceuticals globally. Our Passion for offering excellent pharmaceuticals does not mean doing special and extra ordinary things , But doing day to day operations in a ordinary way with precise care and excellence.
UMAVIDA Pharma Pvt Ltd . state of the Art Pharmaceutical formulation company (at Borisana , Thol-Kadi Road) and infrastructure confirming to EU / PICS /WHO GMP guidelines in OSD & Liquid Oral under its expansion program requires.
Sr. Manufacturing Chemists
Experience :
• 5-6 years of minimum experience in production, should be handling a team and must have worked in Oral Pharmaceutical Formulations ( Mandatory)
• Must have sound working knowledgo on cGMP guidelines like ICH, ISD, WHO. Schedule M etc.
• Familiarity and exposure with cGMP audits like Local FDA, CDSCO, PICS 1.Tablets 2.Capsules & Dry Powders 3. Liquid Oral Department
Qualification : FDA Approval
Purchase Assistant
Job Profile :
• Source wide-range of products (domestically and internationally) in the pharmaceutical & Nutraceuticats Build and maintain trusted relationships with both domestic and global suppliers
• Negotiate pricing and contracts with suppliers with respect to cost, quality, documentation, and lead time Understand and react to domestic & international trends in commodities, raw materials and innovative ingredients to help recommend new products and ideal purchase timing for the company Other functions as needed Requirements:
• Excellent communication and negotiation skills required Proficient in Microsoft Office systems such as Excel and Access
• Willing to travel when needed to conduct inspection of manufacturer & supplier facilities globally
Junior Regulatory Affairs Officer
Job Profile
• By making an important contribution to the development and licensing of products and ensuring their compliance with the requirements of regulatory authorities. Furthermore, they prepare comprehensive documentations of products, including product information for packaging and package inserts, required for the approval for market entry by the authorities.
• Ensuring the compliance of new products with regulatory requirements
• Preparation of comprehensive documentations of complete product development processes
• Communication with regulatory authorities
• An academic degree in science/Pharmacy
• Industry experience and knowledge of regulatory affairs
• Good English skills
• Team spirit and resilience
• Strong management and communication skills
Location : Borisana (Thol- Kadi Road), Gujarat
Mail your resume to : hr@umavidapharma.com mentioning the post applied for in the subject line.
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