The leading edge of Hetero Group, Hetero Biopharma, is steadily establishing itself as a path breaking Biosimilar developer. As a strong R&D driven company offering some of the blockbuster Biosimilar Drugs, we at Hetero Biopharma are bringing about a paradigm shift in the way patients suffering from various chronic conditions are treated.
PRODUCTION - BM (Downstream and Upstream)
• Should have exposure in Single use & SS Bioreactor
• Should have exposure in QMS documentation
• Should have exposure in Chromatography system at manufacture scale
• Should have exposure in different types of filtrations
REGULATORY AFFAIRS
• Experience of dossier filing and obtaining registrations in CIS, LATAM, MENA & ASEAN regions.
• Experience in handling regulatory life cycle management in CIS, LATAM, MENA & ASEAN regions.
• Experience in handling multiple projects and managing regulatory communication with clients.
• Great chance for proactive, smart & able players to be part of successful Regulatory team with 40+ country approvals for biosimilars.
A-RD (Technical position)
• Ability to lead early stage product development.
• Exposure in analytical method Development, qualification & Technology Transfer.
• Should have exposure in stability assessment.
• Handling of HPLC, UPLC, CE, Spectrometry.
• Exposure in Bio-similarity assessments
A-RD (Documentation and control Lab)
• compliance and material management
• Responsible for document review.
• POC for A-RSiD and RA, DQA, QC.
• Responsible for ALCOA in lab
Qualification : M.SC (Biotechnology, Biochemistry, Microbiology) M.Tech / B.Tech (Biotechnology)
Experience : 2 -10 Yrs
Job Location : Jadcherla, Telangana
Walk in Interview
Date : 27th & 28th November 2021
Time : 9.00 a.m. to 4.00 p.m.
Venue : Ginger Ahmedabad (SG Road)
Address: 10/2, Sarkhej - Gandhinagar Hwy, opp. The Grand Bhagwati, Bodakdev, Ahmedabad, Gujarat 380054
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