Thoroughly analyze and critically interpret data to determine the best approach to composing each document. Participate in meetings related to key MW, QC, and compliance activities
VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.
Requirement of Manpower for Manufacturing (Vial, Cartridge, PFS & BFS)
Leben Life Sciences Pvt. Ltd is an established pharmaceutical formulation company for more than four decades. LLS has following openings for its EU-GMP Approved Global Standard OSD and Semi-solids Formulation manufacturing facility at Akola
Candidate should have the command over the subject with first class throughout the Academics, Good teaching, and professional experience, Published work, such as research papers and technical reports
Familiar with cGMP guidelines and Quality Systems as per the international regulatory requirements. Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques.
Define, organize, plan and execute analytical activities and materials characterization of pharmaceutical injectables in compliance with current international/ regional/ national regulations with the support of senior colleagues and team members.