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Clinical research courses

  • Work as Regulatory Affairs PLCM Executive at Apotex Inc

    A Post-graduate, Graduate degree in Chemistry, Pharmacy, Life Sciences. Candidate should have knowledge about Post-approval change submission requirement and compilation of variation packages for US, CAN, EU, AUS-NZ, ROW markets.
  • Work as RA Intelligence Principal at West Pharmaceutical Services
    Bachelors, Master degree or PhD in science, math, engineering or related discipline; The Principal, Regulatory Affairs, Intelligence, Materials is expected to perform with minimal supervision and is an experienced and detail-oriented professional with expertise in materials and with an understanding of the interplay of materials and medical devices, pharmaceuticals and combination products.
  • Interview for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs, Production, QC at Bharat Parenterals Ltd
    Dossier and document preparation as per CTD,ACTD and country specific guidelines, Review of dossiers, DMF and Technical documents, Answer query raised from regulatory authority, package insert, SmPC, PIL & MSDS preparation
  • Job Openings for Regulatory Affairs at Titan Laboratories - M.Pharm, B.Pharm Apply
    They have to make dossier, Review the documents. Should have the knowledge of making CTD, ACTD and courtly Specific dossier.
  • Work as Senior Specialist Regulatory Affairs at Beckman Coulter Diagnostics
    Sr. Specialist Regulatory Affairs will independently, with minimum supervision, initiate and prepare the regulatory submissions, interact with Business Units Regulatory affairs teams and interact with regulatory agencies/health authorities to obtain and maintain product approvals with a focus on India, Sri Lanka and other SWA Countries, as per the country specific regulations.
  • Job for Fresher B.Pharm, M.Pharm in Regulatory Affairs PLCM at Apotex Inc
    A Graduate, Post graduate in Pharmacy. Collation, compilation and timely dispatch of required regulatory documentation to Apotex affiliates/customer and follow-up on timely submission of applications to the health authority.
  • Invites Application for Academic Staff at National Forensic Sciences University
    Ph.D. in relevant discipline with first class or equivalent at the preceding degree i.e. Master Degree in Pharmacy, Forensic Pharmacy with specialization in Pharmacology or relevant discipline with very good academic record throughout.
  • Aurobindo Pharma Hiring Regulatory Affairs Expert

    Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

    Positions open for Regulatory Affairs Expert

  • Torrent Pharma looking for Research Scientists - M.Pharm, MSc Apply
    M.Pharma, MSC with 3 to 8 years of relevant experience HPLC, GC method development for OSD having exposure to regulated, Semi Regulated & India markets including
  • Work as Senior Regulatory Affairs Associate 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 - Biologics

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