- job summary: We are seeking a dedicated Reliability Performance Engineer to develop and execute testing documentation and scripts that validate and verify both physical and digital medical products. This role is pivotal in ensuring product reliability, security, and performance under various conditions, including high-volume simulations and network interactions. This is a Hybrid role. In office Tuesday - Thursday, Remote option Monday and Fridays locajob summary: We are seeking a dedicated Reliability Performance Engineer to develop and execute testing documentation and scripts that validate and verify both physical and digital medical products. This role is pivotal in ensuring product reliability, security, and performance under various conditions, including high-volume simulations and network interactions. This is a Hybrid role. In office Tuesday - Thursday, Remote option Monday and Fridays loca
- job summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertisejob summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertise
- job summary: REGULATORY AFFAIRS MANAGER | 100% Remote (EST Coast based) We're supporting a high-impact Regulatory Submissions Delivery role focused on US and EU regions, with global scope. What we're looking for: 3-5 years of Submission Delivery Support experienceStrong knowledge of US & EU regulatory requirementsBackground in publishing and vendor management a big plusExperience with NDA/MAA filings and larger submissionsSkilled in lifecycle submissionjob summary: REGULATORY AFFAIRS MANAGER | 100% Remote (EST Coast based) We're supporting a high-impact Regulatory Submissions Delivery role focused on US and EU regions, with global scope. What we're looking for: 3-5 years of Submission Delivery Support experienceStrong knowledge of US & EU regulatory requirementsBackground in publishing and vendor management a big plusExperience with NDA/MAA filings and larger submissionsSkilled in lifecycle submission
- job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meetjob summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
