Jobs at ProPharma

Build global talent pipelines for Quality & Compliance specialists and other life sciences functions, including Regulatory, Pharmacovigilance, Clinical Research, and Audit. Engage passive candidates, establish initial relationships, support the wider Talent Acquisition team, and source candidates across the US, EU, JAPAC, and LATAM using LinkedIn Recruiter and potentially Workday ATS.

The GXP Auditor will provide auditing expertise to ensure compliance with regulatory standards in biotech, medical device, and pharmaceutical sectors.

Lead and perform pharmacovigilance benefit-risk activities including authoring and quality-review of aggregate safety reports (PSURs/PBRERs, PADERs, DSURs), RMPs, and signal management reports; conduct literature screening and data extraction; generate and QC line listings; mentor staff; support audits/inspections; liaise with clients and ensure timely, regulatory-compliant deliverables.

Provide SME analytical leadership for a pegylated enzyme therapeutic program. Design and manage analytical strategy, lead SEC-HPLC/SEC-HPMC method development and Phase 3 validation, assess analytical risks and mitigations, contribute to project/scientific teams, and support the client across program activities on a remote contract basis (initial 6 months, likely extension).