• Work as Regulatory Affairs Manager at AstraZeneca
    5 November 2024

    Work as Regulatory Affairs Manager at AstraZeneca

    The Regulatory Affairs Manager II is fully proficient in applying established standards and performs regulatory affairs management for moderately to highly complex international market submissions in all regions with minimal coaching. They are expected to facilitate strategic input, provide proactive contribution to submission planning, identify areas for continuous improvement, and lead cross-functional activities. They participate in the continuous improvement of processes and tools, systems.
  • Work as Associate Manager / Manager - Regulatory Affairs at Zydus Lifesciences
    31 October 2024
    Work as Associate Manager / Manager - Regulatory Affairs at Zydus Lifesciences
    The job requires review of documents related to DMF submission against predefined checklists and submission to various agencies globally.  Should keep the all the regulatory database up to date. Candidate must possess do it right the first-time approach with proven track record. 
  • Opening for Regulatory CMC Senior Specialist at Merck
    22 October 2024
    Opening for Regulatory CMC Senior Specialist at Merck
    Awareness of global pharmaceutical legislation specifically linked to regulatory CMC aspects in the ICH countries. Excellent written and spoken communication skills in English
  • Work as Associate Regulatory Affairs Director at AstraZeneca
    17 October 2024
    Work as Associate Regulatory Affairs Director at AstraZeneca
    As an Associate Regulatory Affairs Director I, you will be a key contributor to regulatory submission strategy, identifying submission risks and opportunities. You will lead regulatory applications and manage procedures through approval.
  • Hiring M.Pharm, MSc Candidates in Regulatory Affairs at Torrent Pharma
    16 October 2024
    Hiring M.Pharm, MSc Candidates in Regulatory Affairs at Torrent Pharma
    Seasoned experience in handling of various EU procedure like DCP, MRP, National. National phase handling for EU procedures. Post approval variation compilation and filling to various EU agencies
  • Teva looking for Regulatory Affairs Associate - M.Pharm, B.Pharm, MSc Apply
    14 October 2024
    Teva looking for Regulatory Affairs Associate - M.Pharm, B.Pharm, MSc Apply
    Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable
  • PAREXEL Hiring Regulatory Affairs Consultant, Associate, Senior Associate
    10 October 2024
    PAREXEL Hiring Regulatory Affairs Consultant, Associate, Senior Associate
    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 M.Pharm, B.Pharm as Regulatory Affairs professionals at BDR Pharma
    10 October 2024
    Job for M.Pharm, B.Pharm as Regulatory Affairs professionals at BDR Pharma
    Regulatory Affairs professionals with 5 to 8 years of experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets.
  • Takeda looking for Regulatory Affairs Manager - MSc, B.Pharm Apply
    6 October 2024
    Takeda looking for Regulatory Affairs Manager - MSc, B.Pharm Apply
    Bachelors in Pharmacy or Masters in Chemistry, Sciences, Biotechnology ,Biomedical Engineering; Provide regulatory metrics on performance that are aligned with Area & GEM Regulatory Affairs criteria to measure regulatory performance to LOC, Area & Regional management
  • Remote jobs in regulatory affairs at PAREXEL
    1 October 2024
    Remote jobs in regulatory affairs at PAREXEL

    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 : Senior Regulatory Affairs Associate (Labelling)

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