(M.S., MPH, Ph.D., or similar degree) in the health sciences, lifesciences, clinical sciences or biomedical engineering...
Summary: Senior Process Engineer to support process and utility systems within a regulated biopharmaceutical manufacturing environment at our Holly Springs site. This role is fully onsite and requires strong hands-on technical expertise w...
successful 510(k) clearances and CE marking is required Strong understanding of medical device product life cycle and regulatory...
Job Description: We are seeking a detail-oriented Field Action Remediation Specialist to implement remote software and firmware deployments, configure devices in RSS, and perform other remediation activities. This role requires deep techn...
management, particularly in the oncology field. Requirements: Bachelor's degree in LifeSciences, Computer Science...
Job Description: Regulatory Affairs Specialist with working knowledge of FDA, and CE marking requirements for IVD products. Client is currently transitioning from IVDD to IVDR (In Vitro Diagnostic Regulation). The RAS is responsible for ...
degree (M.S., MPH, Ph.D., or similar degree) in the health sciences, lifesciences, clinical sciences or biomedical...
Job Description: This individual will oversee an Electronic Batch Record (EBR) implementation project that began in Q4 2025. The current Project Manager will provide knowledge transfer and onboarding prior to transitioning out of the rol...
Roles & Responsibilities: Performs work under general supervision. Provide quality, technical support and oversight during manufacturing activities. Review executed batch records and evaluate product and facility deviations;draw conclu...
Job Description: Regulatory Affairs Specialist with working knowledge of FDA, and CE marking requirements for IVD products. Client is currently transitioning from IVDD to IVDR (In Vitro Diagnostic Regulation). The RAS is responsible for ...