Join us at AstraZeneca, a global biopharmaceutical company with a focus on innovation and collaboration. We are currently seeking a Director of Strategic Advice for our R&D Quality Assurance team. This role is based in our Gaithersburg MD offices, designed to foster collaboration and innovation. Our commitment to sustainability and tackling global health challenges makes AstraZeneca a fulfilling place to work.
In this role, you will be responsible for providing leadership and strategic direction on quality and compliance related to clinical activities. As the independent second line R&D quality assurance function, you will partner with stakeholders in R&D and provide leadership in influencing strategic direction on quality and compliance. You will investigate critical Quality Issues and deliver end-to-end regulatory inspection strategy and management. This role requires a high degree of integrity, strategic thinking, agility, a 'solutions focused' attitude, and the ability to generate simple solutions to complex challenges.
Business Partnering
Leading strategic direction of good clinical practice (GCP) and/or good pharmacovigilance practice (GVP) quality and compliance through engagement with defined customer groups.
Providing effective compliance reporting to senior management and supports strategic QA governance forums.
Supporting quality and compliance risk management for collaborator groups.
Inspection
Providing QA oversight and leadership for managing regulatory GCP/GVP inspections.
Delivery of end-to-end GCP/GVP inspection strategy for key regulatory authority inspections
CAPA
Leading or participating in the investigation of critical quality issues and ensures timely reporting of issues to relevant authorities.
Supervising significant CAPAs for activities in R&D.
Essential Skills/Experience:
A B.S. Degree in Biology or related STEM field.
5 plus years' experience in pharmaceuticals, biotechnology, or a related industry.
A thorough understanding and experience of GxP and quality assurance/management.
Working knowledge of GCP/GVP and health authority regulations and guidelines (e.g., MHRA, EMA, FDA, PMDA.)
Excellent analytical, written, and oral communications skills.
High ethical standards, trustworthy, operating with absolute discretion.
Strong collaborative, influencing and interpersonal skills - curious to understand business environment.
Skilled at managing and using technology.
Ability to maintain and build professional networks.
Experience in managing regulatory health authority GxP Inspections.
Desirable Skills/Experience:
Project management experience.
Knowledge of six sigma/lean/process improvement tools.
Audit expertise.
Understanding of Quality Management Systems.
Experience in digitalization.
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.
The annual base pay (or hourly rate of compensation) for this position ranges from $143,859 to $215,789. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
At AstraZeneca, we follow the science to explore and innovate. We are driven by our desire to understand and reveal new insights into the world's most complex diseases. Our inclusive environment encourages creativity and resilience, allowing us to push the boundaries of science to deliver life-changing medicines. We are committed to making an impact on patients' lives globally and improving access to healthcare. If you are passionate about science and want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be.
Ready to make a difference? Apply today!
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.
