Having Injectable Experience of Shop floor Supervising activities like Aseptic Filling, Autoclave Operations, Compounding vessels operations, Manpower Planning, Change Controls, investigations, CAPA, Vial Washing, Lyophilizers and Training and QMS
Endo India Par Formulations is a pharmaceutical company that develops, manufacturers and markets safe, innovative and cost-effective pharmaceuticals that help improve patient quality of life. At Endo our investment in state-of-the-art equipment and facilities, commitment to ethical standards, and growing portfolio of products makes us a company where you can enjoy a productive career with long-term potential.
Exposure of handling and compliance of various compression, coating and granulation machines, equipment Online documentation of BMR and log books during execution of batches.
M.Pharm, Pharm.D, BDS Postgraduate in registered life Sciences. Min 2 - 4 years relevant experience into Pharmacovigilance case processing and related activities in alignment with patient safety operations.
M.Sc. in Chemistry, Organic Chemistry, Pharmaceutical Chemistry, Medicinal Chemistry or equivalent with National Level JRF eligibility test such as NET, GATE, etc. qualified.
Ph.D, Masters in life sciences from a reputed Institute with 0-2 years relevant experience cell culture, microbiology, molecular biology, zebrafish, mouse handling, mRNA, AAV experience, assay development, high-content imaging.
Master degree in Life Sciences, Biotechnology or related disciplines from a recognized University with 60% or better marks or equivalent grade. A minimum of one-year post-qualification relevant experience.
Graduate Degree in Biotechnology or any Life Sciences subject from a recognized University or equivalent. Postgraduate degree will be preferred Prior experience, in- vitro cultures work along with cell biology assays will be needed.
Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management. Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities