July 2024

Degree in Pharmacy from a recognized University or equivalent, One year experience as Pharmacist Or Diploma in Pharmacy from a recognized University, Institute. Registered as Pharmacist under the Pharmacy Act 1948. It is an institution established for teaching, research and patient care in the area of health. JIPMER spreads over 192 acres.

BSc, MSc in Life Science, B.Pharm, M.Pharm. with Post Graduate Diploma in Clinical Research, Certification in Clinical Research, MSc Clinical Research. M.Sc. Clinical Research Interns of TMH, completing internship in Sept. 2024 can also apply. The Tata Memorial Centre is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines.

Govt Recognized Univ. Degree in Pharmacy or Diploma in Pharmacy or its equivalent qualification obtained from and candidate should be registered with Gujarat Pharmacy Council under Pharmacy Act 1948. Under the National Health Mission and the State Budget, an announcement is hereby made to fill the following staff positions in the district of Kutch on temporary basis

B. Pharma with minimum 01-year experience of working in Dispensary, Pharmacy of the hospital having minimum 100 beds. OR D. Pharma with minimum 3 years of experience of working in a Dispensary, Pharmacy of the hospital having minimum 100 beds.

M. Sc. in Organic Chemistry from a recognized University or equivalent. Synthesis of Reference Standards and in-vitro and in-vivo studies (PK studies) on the metabolites and long-term metabolites; M.Sc. in Biotechnology / Biochemistry / Clinical Biochemistry / Zoology from a recognized University.

M.Pharmacy, preferably a PhD in Pharmaceutical sciences Join team for ground breaking discoveries in Drug Metabolism & Pharmacokinetics; Opportunities for talented individuals to join us as senior research associate/research scientist- In Vivo, senior research associate/principal scientist- In Vitro ADME and research associate/group leader- bioanalysis.

Responsible for Authoring and review of dossiers for submission to US, Canada, Europe, Australia, South Africa and other regulated markets. The Company focused on the emerging markets of Latin America, Caribbean, Francophone and Southern Africa and is today one of the leading suppliers of Pharmaceuticals in these regions, with over 2800 product licenses across the globe.

Review quality Dossiers in CTD format for new Generic drug submissions, in-line with the guidance and templates. Compile responses to deficiencies and deficiency management for the given portfolio of products.

MSC, B. Pharm, M. Pharm; Execute assigned BABE study as per SOP and applicable regulatory guideline. Preparation and Compilation of Essential Document in Trial Master File, review of CRF and Raw data.