PPG JPN ProPharma Group GK

NewBe an early applicant On-siteAPACFull-time

GVP/GCP Auditor, Compliance & Quality Assurance – Japan

Japan

ProPharma is hiring a GVP/GCP Auditor for its Compliance & QA team in Japan: planning and conducting clinical (GCP) and pharmacovigilance (GVP) audits of sites, CROs and vendors, evaluating compliance with Japanese and international regulations, and writing audit reports. Requires fluent Japanese, professional English and life-sciences auditing experience.

AI Corrective Action GCP Networking

NewBe an early applicant On-siteNorth AmericaFull-timeC-level

VP/Sr. VP of Advertising & Promotional Review

United States

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently…

AI Process Improvement

NewBe an early applicant On-siteAPACFull-time

Freelance/Contract Scientific Business Analyst

Australia

ProPharma is hiring a freelance/contract Scientific Business Analyst near Melbourne (hybrid) to support a key life-sciences client in its Digital Transformation group through June 2027. Day to day: gathering requirements, mapping scientific lab workflows into technology solutions, validating systems, and training users.

AI Requirements Gathering

NewBe an early applicant On-siteNorth AmericaFull-time

IT Access, Automation, and System Administrator

United States

Internal IT role at pharma consulting firm ProPharma: handling user access management tickets via Active Directory (with PowerShell scripting) and serving as system administrator for a global ITSM service desk (ManageEngine ServiceDesk Plus) — designing workflows, automations, integrations, and reporting.

Active Directory AI Analytics API Automation +7 skills

NewBe an early applicant On-siteEuropeFull-timePrincipal

3 days ago

Freelance/Contract Principal Quality Assurance Consultant

Sweden

Contract Principal Quality Assurance Consultant supporting an urgent pharma client project in Uppsala, Sweden for at least 3-4 months full time, largely onsite. Day to day: reviewing quality systems for regulatory compliance, supporting CAPA and investigations, QA review of manufacturing activities, and driving inspection readiness including mock audits.

New On-siteNorth AmericaFull-time

4 days ago

Executive Assistant & Medical Affairs Project Coordinator (Onsite, Wilmington, DE)

United States

Executive assistant and project coordinator supporting three Medical Affairs leaders (including the Group Vice President) at pharma consultancy ProPharma. Day to day: calendar, email, travel and expense management, meeting/event logistics, budget and accrual tracking, SharePoint upkeep, and project coordination using MS Office, Outlook, SharePoint, and DocuSign.

AI SharePoint

AI Corrective Action Onedrive SharePoint

5 days ago

Project Director

New On-siteUKFull-time

United Kingdom

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently…