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Regulatory affairs

 

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  • Opportunity for M.Pharm to Join Indian Pharmacopoeia Commission as Complaint Executive

    Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. Its basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP).

  • Regulatory Affairs Specialist Require at Medtronic
    Prepare, review, file, and support premarket documents for global registrations for assigned projects. Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.
  • AstraZeneca Hiring Regulatory Affairs Manager - B.Pharm, M.Pharm Apply
    Developing India-specific Artwork, Support Regulatory dossier preparation and Submissions like New drug applications, Site registration, clinical trial and Import licence. Managing Registration samples right from dispatch of samples till the report. Licence Life cycle management. Adequate representation in SEC
  • Sanofi looking for Regulatory Affairs Manager
    The Regulatory Manager is a scientific leadership role that leads the regulatory activities involved in the India, Srilanka, Nepal, Maldives market. The role provides the regulatory strategies, and regulatory submissions of new products for various brands in Rx, OTC, Food supplements in support of the new and existing portfolio
  • Enzene Bioscience's Walk-in Drive for M.Pharm, MSc, MTech in Multiple Department
    Mammalian and Microbial (Upstream Process): Media preparation, Filtration, Aseptic technique, Inoculum Handling, Handling of SU bioreactor/RM, Perfusion technology, upstream analytical instruments. Handling of SS Fermenter, Continuous centrifuge
  • ADVANZ PHARMA looking for Regulatory Affairs Executive
    Assessing Change request assigned to ensure regulatory assessment along with strategy and documents required for any regulatory submissions are shared with stakeholder in a timely fashion.
  • Join PAREXEL as Regulatory Affairs Associate

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.

    Post : Regulatory Affairs Associate

  • Walk in Drive for M.Pharm in Regulatory Affairs Department at Sun Pharma
    Compile registration dossiers for submission to various health authorities like – USA, Canada, Europe, Australia and Israel. Prepare responses to deficiency letters received from various agencies.
  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department at Biocon

    Biocon is global biopharmaceutical company changing patients' lives in over 120 countries by finding new and affordable ways to treat diabetes, cancer and autoimmune diseases. Biocon is a research-driven, global healthcare company with a strong matrix of capabilities along the biopharmaceutical value chain.

    Department : Regulatory Affairs

    Experience : 3-12 years
    Qualification : M.Pharma / M.Sc / B.Pharma
    Job Location : Bangalore

  • Hetero Drugs Interview for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department

    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.

    Walk-in Interviews for Regulatory Affairs

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