Director of Quality Assurance and Compliance

hace 2 días


Palma, Baleares, España Biorasi A tiempo completo
About the Role

Biorasi is seeking a highly experienced and skilled Associate Director of Quality Assurance to join our team. As a key member of our Clinical Operations department, you will be responsible for leading the development, implementation, and maintenance of our Quality Systems and Standard Operating Procedures (SOPs).

Key Responsibilities
  • Lead the development, implementation, and maintenance of GCP Quality Systems and SOPs.
  • Train and mentor staff on global GCP regulations and guidance.
  • Provide QA oversight and auditing of eTMFs.
  • Lead and/or oversee consultant-mediated audits; develop, recommend, and follow up on corrective actions.
  • Lead preparations for Clinical Operations (corporate and third-party) inspection-readiness.
  • Lead and manage GCP Inspections on behalf of Biorasi and Biorasi clients.
  • Serve as an SME for areas of responsibility during regulatory inspections, and directly manage inspection Ready-Room activities.
  • In partnership with the Clinical Operations, Regulatory, and Pharmacovigilance teams, design and implement a risk-based clinical Quality Assurance management system.
  • Identify QA and compliance-related issues and implement solutions to ensure timelines are maintained.
  • Establish metrics and report the state of GCP Quality and compliance of clinical trials to senior management.
  • Ensure Clinical Operations activities are compliant with cGCP, cGLP, FDA, ICH, EMA regulations and guidelines and industry standards.
  • Provide consultation in interpretation of regulations/guidelines, as they apply to GCP practice, awareness of regional regulatory requirements, and phase of study.
  • Keep abreast of industry developments – forthcoming regulations, guidance, best practices, etc.
  • Ensure that Biorasi quality systems, processes, and procedures are compliant with applicable regulations and ICH guidelines.
  • Ensure that Biorasi standard operating procedures (SOPs) are compliant with applicable regulations and guidelines.
  • Oversee the planning and conduct of internal, investigator, and vendor Quality Assurance audits.
  • Manage the administration of Quality Assurance files and the control of central files.
Requirements
  • Degree in biomedical sciences or related scientific discipline.
  • 10+ years in drug development or clinical research within the pharmaceutical industry or CRO with at least three years in quality assurance, quality management, or clinical safety-related area of responsibility.
  • Strong planning, leadership, negotiation, communication, and presentation skills.
  • Experienced with auditing clinical vendors and investigator sites.
  • Practical knowledge of GCP or GMP, and FDA regulatory structure.
  • Proficient with Microsoft Office tools.


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