Role Summary
Director Strategic Advice โ R&D Quality Assurance, focused on influencing strategic directions on quality and compliance as the GVP/GCP expert for clinical and post-market activities within a science-driven environment.
Responsibilities
- Work closely with R&D stakeholders to provide leadership in influencing strategic direction on quality and compliance through GCP/GVP expert advice related to clinical and post-market activities including risk management.
- Deliver end-to-end regulatory inspection strategy and management.
- Manage relationships with defined stakeholder groups and senior leaders in R&D for the strategic development and delivery of a GxP risk-based, robust quality assurance program and quality management activities.
- Lead or participate in investigations of critical quality issues and ensure timely reporting to relevant authorities where applicable.
- Lead training for colleagues and business stakeholders.
- Support or lead the development and/or revision of QA processes, projects, and tools.
- Generate simple solutions to complex challenges with a solutions-focused attitude.
Qualifications
- Bachelorโs degree required; Masterโs degree preferred.
- 10+ years of experience in pharmaceuticals or a related life-science industry.
- Thorough understanding and experience of GxP (GVP and GCP) and quality assurance/management.
- Strong collaborative, influencing, and interpersonal skills; curious to understand the business environment.
- Excellent analytical, written, and oral communication skills.
- Proficient in written and spoken English.
- High ethical standards, trustworthy, operating with absolute discretion.
- Skilled at managing and using technology; curious regarding AI.
- Ability to maintain and build professional networks with stakeholders.
- Experience in managing regulatory health authority GxP inspections.
Desirable
- Project management
- Key Account management
- Experience in Six Sigma/Lean/Process improvement tools
- Quality and Audit expertise