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🥝 RA Officer (Associate Consultant)

ProductLife Group | India, India | Posted June 18, 2026

Job Description

Specific activities and responsibilities:

  • Provide support to clients on the registration and listing of pharmaceuticals, biologicals and medical devices in Australia and New Zealand and (JAPAC) region.

  • Provide support to clients with the maintenance of current registrations and listings.

  • Provide eCTD publishing support.

  • Review, critically evaluate, prepare and submit regulatory dossiers to the TGA and Medsafe.

  • Assist clients in responding to TGA and Medsafe questions.

  • Assist senior members of the team in the preparation of complex regulatory applications for submission to the TGA and other regulatory agencies.

  • Assist with project and client management as required.

  • Management and preparation of GMP clearance applications for submission to the TGA and/or other regulatory agencies, as required.

  • Preparation, review and update of quality documentation.
  • Requi...

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