• Vacancy for M.Pharm, MSc in Regulatory Affairs Department at Torrent Pharma
    17 May 2024

    Vacancy for M.Pharm, MSc in Regulatory Affairs Department at Torrent Pharma

    Dossier submission and review of Module 1, 2 and 3. ANDA submission. DCP, MRP, National Filing for various EU countries. Formulation regulatory for solid orals, Topicals, Ophthalmics, Solutions. Experience in management of life cycle and post approval variations. Experience of communication with agencies.
  • Work as Regulatory Affairs Senior Manager at ADVANZ PHARMA
    17 May 2024
    Work as Regulatory Affairs Senior Manager at ADVANZ PHARMA
    Helping the team with strategic planning for submissions, focussing on right classification of variation with an emphasis on urgency of change, nature of change, optimising submission cost, timelines for approval and any risk assessment needed.
  • Sandoz looking for Quality Operations Associate Manager
    17 May 2024
    Sandoz looking for Quality Operations Associate Manager

    Sandoz become a standalone organization! As a global market leader in Generics and Biosimilar medicine, Sandoz is stepping forward from a position of strength! Those joining Sandoz in the coming months will help shape the future of the company, it’s growth, innovation, culture and how Sandoz impacts the lives of millions. These will be careers with genuine impact! This is one such role.

    Post : Associate manager - Quality operations (GQS-I)

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department at Hetero Drugs
    16 May 2024
    Walk in Drive for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department at Hetero Drugs

    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.

    Openings for Regulatory Affairs

  • JAMP group Hiring Regulatory Affairs Manager - B.Pharm, M.Pharm Apply
    15 May 2024
    JAMP group Hiring Regulatory Affairs Manager - B.Pharm, M.Pharm Apply

    The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products.

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Production, QC, Regulatory Affairs at SMS Pharma
    15 May 2024
    Walk in Drive for M.Pharm, B.Pharm, M.Sc in Production, QC, Regulatory Affairs at SMS Pharma
    Experience in API production activities like Handling of Reactors, Centrifuges, Driers, GMP.GDP & Safety practices
  • Work as Senior Regulatory Affairs Associate at PAREXEL
    15 May 2024
    Work as Senior Regulatory Affairs Associate at PAREXEL
    Contribute to preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.
  • Job for B.Pharm, M.Pharm in Regulatory Affairs at JAMP group
    12 May 2024
    Job for B.Pharm, M.Pharm in Regulatory Affairs at JAMP group
    B.Pharm / M.Pharm; Preparation of responses to clarification requests received from Canadian authorities. Communicate with external suppliers for the preparation of packaging components and ensure technical feasibility.
  • Opportunity for M.Pharm, B.Pharm, MSc to Join Novo Nordisk as Regulatory Professional
    12 May 2024
    Opportunity for M.Pharm, B.Pharm, MSc to Join Novo Nordisk as Regulatory Professional
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide.
  • Regulatory Affairs Trainee Require at Apotex
    12 May 2024
    Regulatory Affairs Trainee Require at Apotex
    Perform all the labelling update activities and tracking in systems for record maintenance with respect to New Product Development NPD label creation and Product Life Cycle Management PLCM update for products in USA and Canada market
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