Product Life Group

Join ProductLife Group as a Data Officer in Pharmacovigilance. Utilize your 2+ years of PV experience and knowledge of UK/EU regulations to manage safety case processing and ICSR follow-up. This remote role in the Philippines requires working UK hours, offering a key position within a dynamic, cl...

Seeking a Local Safety Specialist to ensure pharmacovigilance compliance in the Benelux region. Act as the key local contact for authorities, managing PV case processes and regulatory submissions. Requires 5+ years of PV experience, fluency in French/Dutch, and strong knowledge of Benelux regulat...

Join our MI Department as a Medical Information Officer. This role requires fluent French and Dutch, along with a scientific diploma or degree. You will handle medical information requests, manage vigilance cases, and draft responses. Prior experience in a similar field is a strong advantage.

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 an Equity Compensation Expert to manage investment and bonus programs at Product Life Group. You will administer equity plans, ensure legal/tax compliance, and liaise with HR, Finance, and Legal. Requires 5+ years in equity administration, PE experience, and strong Excel skills. This is a...

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...

Lead the accounting operations for French entities at ProductLife Group. This Paris-based role requires expertise in French GAAP, IFRS, and tax compliance, plus experience with NetSuite. You will manage a team, oversee month-end closing, and drive process improvements in a dynamic international e...

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...

Seeking a Digital Consultant with a background in pharma, microbiology, or IT. You will configure and support LabVantage LIMS, ensuring compliance with GxP and FDA regulations. This role involves system testing, user support, and data migration for US-based life sciences clients. Prior lab proces...

Join ProductLife Group as a French-speaking Medical Reviewer. Utilize your MD in Dermatology and 5+ years of pharmacovigilance experience to assess case safety. You will apply expertise in GVP, FDA, and cosmetic regulations within a supportive, global environment. Enjoy flexible work arrangements...