Product Life Group

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 – Life Science Consulting in Italy. Drive digital transformation for pharma, biotech, and medical device clients. Leverage your STEM background and GxP expertise to implement cutting-edge software solutions (MES, LIMS, QMS). Based in Florence, Milan, or Rome, you’ll advise on co...

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-...

Join PLG as a Regulatory Affairs Specialist in India. Ensure UK & EU compliance for medicinal products, managing MAAs, lifecycle maintenance, and post-approval activities. Ideal candidates have 3-7 years' experience with MHRA/EMA, CTD/eCTD, and regulatory systems. This role offers a dynamic envir...

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...

Lead global regulatory strategy as a client-facing RA Strategy Expert. Utilize your 10+ years of experience with EMA, FDA, and large molecules to oversee submissions from CTAs to MAAs. This strategic role in the Netherlands offers full project ownership and mentorship opportunities within a globa...

Join PLG as a Regulatory Affairs Specialist in Poland. You will manage the full product lifecycle, ensuring global compliance for medical products. The role requires 5-10 years of Polish market experience with MAA, CTD, and post-approval processes. Fluency in English and Polish is essential for t...

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 ProductLife Group as an Information and Documentation Officer in India. Utilize your pharmacy/life sciences degree and pharmacovigilance knowledge to perform critical literature monitoring. You will conduct searches in PubMed/ADIS, manage documentation, and support quality systems. This role...

Lead pharmacovigilance projects for a diverse client portfolio in this key Project Lead role. Utilize your 3+ years of safety experience and project management skills to ensure compliant delivery and client satisfaction. Enjoy a flexible hybrid model in Melbourne or Sydney while making a meaningf...