Director, Development Asset Quality Strategy

hace 2 meses

Barcelona, España Tradevest Gmbh A tiempo completo

As part of the Development Quality Team, you will drive Quality Culture with Development, Regulatory and Safety stakeholders, through learning, embedding a quality mindset, and executing on continuous improvement opportunities. You will be responsible for managing business relationships with defined clinical development stakeholder groups and senior leaders in Development, Regulatory and Safety and for the strategic development and delivery of a GCP risk based robust quality management activities for these stakeholders. The Director will mentor junior team members as well as provide guidance when dealing with high risk complex GCP issues. The Director will lead departmental process improvements and support cross functional process improvements.
You will be responsible for:
Development and execution of the overarching strategy related to proactive and sustainable quality and compliance for assigned areas.
Where applicable, represent DQA on Alexion Global Program Teams (GPTs) and Regulatory Strategy Teams (RSTs) to proactively identify critical to quality risks and mitigation strategy to drive excellence in study design and execution and to minimize risk to regulatory submission/approval
Proactively identify Key Quality and Risk Indicators (KQIs/KRIs) for assigned areas and develops mechanisms of KQI/KRI, detection, oversight and trending with relevant stakeholders
Work with Development Quality peers to ensure escalation of risks and issues identified at a study level to relevant stakeholders
As required, provide guidance to junior team members for global/systemic clinical quality issue investigations
Mentor new and existing employees as per established on-boarding plan and on focus improvement areas.
Work with cross functional and other quality partners to proactively identify areas of risk, improvement, or KPI/KQIs, as applicable
Serve as the quality expert for global/systemic clinical quality issue investigations, which includes: In collaboration with issue owners lead Quality Event reportability assessments, investigations and Root Cause Analysis
Perform Quality Event risk assessments and trending (deviations, audit findings, inspection findings etc.) to determine robust CAPAs
Acts as quality approver for Quality Issues and CAPAs as assigned

Be accountable for leading inspection readiness as assigned including but not limited to: Provide leadership and guidance to team members in promoting a culture of inspection readiness and sustainable clinical compliance
Provide guidance to team members in Inspection Readiness and Preparation Activities (e.g., SME training, Mock inspection etc.)
Support follow up and tracking of inspection commitment and effectiveness checks

Serve as the Subject Matter Expert (SME) and provide guidance on major processes/platforms optimization and quality governance requirements where applicable
Participate in and compile data for quality management reviews, risk reviews, and other study/TA/Asset level quality reviews
Drive continuous improvement and knowledge management by sharing case studies/lessons learned from QA activities to minimize recurrence of similar issues
Actively participate in meetings driving quality and business performance
Support Due Diligence and integration activities as assigned
Lead Sponsor Inspections and Drive CAPA development
You will need to have:
Bachelor's degree in life science, or equivalent field, required
Minimum of 12 years of experience in clinical research area inclusive of, but not limited to, Good Clinical Practice or Good Clinical Practice quality assurance and compliance
Established knowledge of GCP regulations and guidelines (EMA, FDA, PMDA etc.)
Significant experience with GCP investigations, risk assessments and CAPA management
Extensive experience in Project Management and leading cross functional initiaves
Experience participating in GCP regulatory inspections
Experience with multinational products and regulations as well as with mandated risk management plans
Experience in training and coaching people
Ability to travel up to 10%
The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
We would prefer for you to have:
Advanced degree preferred
Gene Therapy expertise
Phase 1 expertise
Competencies to be successful for this position include:
Quality, process, and compliance oriented
Strong interpersonal skills
Critical thinking
Integrity
Communication
Teamwork
Problem solving
Risk-based approach mindset
Stakeholder management including senior LT
Location: Barcelona
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
At Alexion, AstraZeneca, Rare Disease, we are a beacon in the global Biopharmaceutical landscape. Our closeness to patients brings us closer to our work and closer to each other. Combined with our brave, pioneering spirit – we are truly unique in R&D and healthcare. Our culture is rooted in integrity, inclusiveness, and our dedication to joining and supporting the communities in which we live and work. We invest in and value people who believe in the importance of our purpose and understand what it takes to deliver on it.
Are you ready to make an impact? To drive change with integrity? To join a team that celebrates diversity, innovation, and the power of connection to patient's lived experiences? If this sounds like a team that you want to be a part of... then we'd love to talk. Apply now
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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