Product Life Group - Consulting

Join our JET Program in Melbourne as a Medical Information Junior Associate. Ideal for recent graduates in Pharmacy or Life Sciences, this two-year role offers hands-on experience with global pharma clients. You’ll handle medical enquiries, conduct literature searches, and support translations. P...

Senior Consultant – Regulatory Affairs role in Florence, Milan, or Rome, Italy. Join ProductLife Group to drive digital transformation in Life Sciences. Requires a STEM degree, 2+ years consulting experience, and fluency in Italian and English. Advise clients on GxP compliance, implement cutting-...

Lead U.S. regulatory strategy for biotech and pharma clients at ProductLife Group. This senior consultant role requires 10-15 years' FDA experience, expertise in INDs/NDAs/BLAs, and direct Health Authority interaction. Provide strategic leadership and act as a trusted advisor in this client-facin...

Join LifeBee as a Digital Life Science Consultant in Italy (Florence, Milan, or Rome). You will advise clients and implement cutting-edge software in GxP-regulated environments. A STEM degree, fluency in Italian/English, and knowledge of IT systems are required. Drive digitalization projects with...

Join our team as a Regulatory Affairs Specialist in Australia. Utilize your 5+ years of RA experience to manage pharmaceutical and medical device submissions for the JAPAC region. You will lead projects, provide strategic advice, and ensure compliance with TGA and Medsafe regulations. This role o...

Seeking a Regulatory Affairs Officer with 3+ years' experience, specializing in TGA and Medsafe submissions. You will manage pharmaceutical and medical device registrations for Australia, New Zealand, and the JAPAC region from India. This role requires strong dossier preparation, eCTD publishing,...

Join our Market & Patient Access team as a Market Access Officer in Australia. Utilize your 2+ years of local experience and strong analytical skills in health economics and reimbursement. You will prepare key submissions (PBAC, MSAC) and develop cost-effectiveness models for pharmaceutical and m...

Launch your career as a VAF 422 Consultant supporting clinical trial systems. This entry-level role requires 0-2 years in BSI and 2-3 years in life sciences, focusing on CTMS configuration, testing, and user support. You will apply ICH-GCP knowledge and assist with system documentation for client...