Teams at ProPharma

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).

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

The Workday Technical Developer is responsible for integrating solutions within Workday, requiring collaboration with teams to gather requirements, maintain existing integrations, and manage the development life cycle.