M.Pharm. or PharmD, Clinical Pharmacology, Pharmacy Practice, Clinical Research. 1-year experience in Pharmacovigilance. Good communication and computer skills.
Exposure of analysis for Finished Products, Stability Samples and Raw Materials. Having Knowledge of Analytical Method Validation, Verification and Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals and Quality process.
Demonstrates a robust scientific approach to laboratory analysis. Regularly utilizes personal experience, academic training, and technical insights, including emerging sciences, to address complex technical issues within the laboratory.
Influences and inspires own team and/or brings matrix collaborators together across the organization with eye for progressing teams towards decision points and deepening scientific understanding.
Plans and coordinates activities to ensure regulatory lifecycle management activities and approvals are achieved by the Local Operating Company in a timely manner for all globally approved products.
Pfizer Inc announced that the European Commission has granted marketing authorization for HYMPAVZI marstacimab for the routine prophylaxis of bleeding episodes in patients 12 years of age and older weighing at least 35 kg with severe hemophilia A
Deciphering the Oncogenic network of Ubiquitin specific peptidase 37 USP37 and its therapeutic potential in prostate cancer. MBBS, BDS, MVSc, M.Pharma, ME, M.Tech degree holders with relevant experience in the cancer research.
Bachelor of Pharmacy Should have experience in working in Hospitals, Clinics, Pharmacies, in case B.Pharma candidate is not available, Diploma in Pharmacy candidates with at least 02 years of experience will be considered. Computer knowledge is mandatory.
First-class postgraduate degree in Zoology, Biochemistry, Biotechnology, Life Science or a related field with the research experience after completing PG or Ph.D. in the mentioned field.
Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Globally renowned, vertically integrated pharmaceutical player engaged in Research and Development (R&D), manufacturing, and marketing of high-quality chemical and biologic medicines across diverse therapeutic areas.
Oversees the development, implementation, and maintenance of the Quality Management System within the Probiotics or Non-Aseptic manufacturing facility. This includes ensuring that all processes, procedures, and documentation comply with relevant regulatory standards such as Good Manufacturing Practices.
B.Pharm, M.Sc, M.Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.
Can handle instrument i.e HPLC- Dissolution 3C, IR,UV, QC QMS, Material testing xposure on EM, water testing, MLT testing of FP and RM/Stability samples , Analysis and review of Micro samples, reports.
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.