Product Life Group - IT - Administration

Seeking an experienced **QPI Expert – Audit Management Lead** in **France** to drive audit strategy and regulatory compliance within the pharmaceutical industry. This client-facing role requires 8+ years in Quality, strong **Pharmacovigilance (PV)** expertise, and **GVP Auditor** qualification. L...

Proposal & Strategic Procurement Engineer sought by ProductLife Group in Florence, Italy. This role requires 5+ years of experience in engineering procurement, vendor management, and strategic sourcing. You will lead technical proposals, coordinate subcontractors, and manage project lifecycles fr...

Join ProductLife Group as an Information and Documentation Officer in India. Ideal for Pharmacy or Life Science graduates with 1-3 years of Pharmacovigilance experience or freshers with PV knowledge. Perform literature searches using PubMed and ADIS databases, support client audits, and ensure qu...

Seeking an experienced Senior Medical Writer in France. This role requires a Pharmacist or Physician with 5-8 years in PV and expertise in Safety databases. You will lead the production of PSURs, PBRERs, DSURs, Risk Management Plans, and Signal Detection reports. Ensure GVP and ICH compliance whi...

We are seeking a Case Specialist with a Doctor in Pharmacy degree and 4-5 years of pharmacovigilance experience. You will perform medical evaluation, quality control, and data entry of vigilance cases in India. Key skills include database proficiency, regulatory knowledge, and strong communicatio...

Data Officer role in India: manage vigilance data with accuracy and compliance. Requires Pharmacy degree, 1-3 years Pharmacovigilance experience, MedDRA coding, and safety database skills. Handle case triage, regulatory reporting, and client communications. Join a detail-oriented team ensuring da...

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...

Lead global regulatory submissions for a top consulting firm. Manage end-to-end eCTD publishing using DocuBridge/EXTEDO, ensuring compliance for NDAs, BLAs, and life-cycle filings. This hands-on expert role requires 8+ years' experience and offers leadership of a publishing team.

Join our global regulatory team as a Publishing Officer. You will compile and publish eCTD/NeeS submissions for international markets in this long-term project role. We seek a detail-oriented professional with 3+ years of regulatory operations and hands-on publishing experience. This remote posit...

Seeking a NetSuite System Administrator & Developer in France. You will configure, administer, and support the NetSuite platform, integrating with Salesforce and Certinia. The role requires 3+ years of NetSuite experience, proficiency in finance processes, and expertise in release management. Joi...