Senior Quality Associate

Role: Senior Quality Associate supporting GMP quality systems within a biopharma focused on pulmonary hypertension therapies, combining proprietary PRINT Technology with established medications. Responsibilities: manage deviation, change control, CAPA, and document systems; support manufacturing and QC operations; develop SOPs; assist in management reviews; monitor quality trends and compliance; promote inspection readiness and continuous improvement. Requirements: Bachelor's in Life Sciences or related field; 2+ years QA experience in regulated industry; knowledge of quality systems, GMP, and regulatory inspections; experience with electronic platforms like Veeva or Kneat preferred; strong organizational, communication, and detail orientation skills. HighValue: GMP compliance, deviation and CAPA management, regulated industry experience, electronic document platforms, pulmonary hypertension therapy focus, inspection readiness. WorkSetup: not specified; requires compliance and quality assurance expertise.