Help push the boundaries of science to deliver life-changing medicines to patients! With science at its heart, this is where breakthroughs born in the lab become transformative medicine - for the world's most complex diseases. Striving to understand the needs of diverse populations and act accordingly, we aim to transform healthcare to secure a future where everyone can access affordable, sustainable, innovative healthcare. Answering unmet needs by pioneering the next wave of science and targeting the drivers of disease to help us create the next generation of therapeutics. With our ground-breaking pipeline, the outlook is bright. Be proud to take your place somewhere that has already achieved so much and is determined to do more.
There is no better time to join our global, growing enterprise as we lead the way for healthcare and society. Join AstraZeneca as a Vice President of R&D; Quality Assurance, Clinical Trial Transparency and Clinical Policy. This role offers the opportunity to establish direction and provide strategic leadership to multiple teams. You will be accountable for the design and compliance of our Quality Management System and framework to relevant regulatory requirements. This role is a chance to lead global teams and support staff, and manage relationships with regulators, industry groups, and external advisers.
ResponsibilitiesLead groups and develop and sustain high-quality organizations that develop and deliver against global processes, and strive to continuously improve in competence, scientific standards, innovation, and performance.Provide assurance across R&D and proactively partner with stakeholders to share data-driven insights, advice, and expertise with the strive to embed a quality mindset and a culture of ethics and integrity.Lead the Quality Review Board activities.Supervise the design, conduct, and reporting of a fit-for-purpose second line risk-based audit program to provide assurance of compliance with GLP, GCP, GVP, Lab GCP, GLS, and HBS.Accountable for the performance and quality of the clinical transparency processes in scope.Provide effective management and escalation of quality incidents and CAPA and provide adequate KPIs/measures to stakeholders, in order to set the direction of quality.Ensure successful conduct of major health authority inspections.Lead the work on developing, improving, maintaining, and making accessible a modern and fit-for-purpose Quality Management System for R&D.Manage headcount numbers and costs to budgetary targets agreed with the Chief Medical Officer.Maintain a current understanding of relevant laws, regulations, and self-regulatory standards and developments and ensure AZ programs evolve to respond effectively to changing government and societal expectations.Line Management activities: Accountable for development of assigned staff and achievement of performance standards, capability, and effective organizational leadership.Optimize the business performance of direct reports to ensure an effective QA organization.Ensure own and staff member tasks are performed to current practices and in accordance with company standards and ethics.Contribute to functional budget management. Minimum RequirementsBachelors Degree required, with preferred Pharmaceutical/Scientific qualification and postgraduate training or equivalent.Extensive experience from the pharmaceutical industry, including at least 5 years in Quality Development with a record of professional achievement and recognition within multiple areas of Pharmaceutical drug development.A broad understanding of the technical/regulatory requirements within drug development and an ability to balance this with industry standards to achieve business goals.Proven leadership and senior line management in the pharmaceutical industry.Extensive industry experience and established networks and acknowledged as a quality assurance expert internally and externally.Proven excellent communication skills and experience of leading teams from different national cultures.Successful management in leading change processes.Proven track record to influence whilst maintaining independent and objective views. Skills and CapabilitiesA broad and comprehensive understanding of pharma industry-related requirements and how they translate to robust compliant and efficient standards.Awareness of the latest developments and interpretations by regulators and industry peers.Experience in working with external providers, collaborators, e.g. from academia and other Pharmaceutical companies.Ability to resolve conflict and deal with a wide range of sophisticated problems independently where highly-developed analytical skills, conceptual thinking, and strategic vision are required, thus representing the highest level of business risk management.Attention to items that matter - passion for simplifications and continuous improvements to support.
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