Director Occupational Toxicology

AstraZeneca•Gaithersburg, MD

9d•Hybrid

About The Position

Are you ready to lead the charge in occupational toxicology within Global Safety, Health and Environment (SHE)? As the Director of Occupational Toxicology, you'll develop strategies and provide expert advice to ensure workplace health risk assessments meet scientific quality and compliance standards across the globe. Your role will be pivotal in shaping the future of occupational toxicology at AstraZeneca! 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 AstraZeneca, we are committed to making a difference beyond patients by pioneering sustainability strategies. With a focus on delivering more medicines faster and more affordably, we thrive on innovation backed by investment and leadership. Join us as we turn molecules into medicines through cutting-edge science, digitalization, and sustainable practices. Ready to make an impact? Apply now to join AstraZeneca's journey towards a healthier future! Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world's most serious diseases. But we are more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We're curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We're driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you'll do work that has the potential to change your life and improve countless others. And, together with your team, you'll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Requirements

PhD in toxicology or related biomedical science field (or equivalent experience).
10+ yrs experience in senior strategic Safety, Health and Environment covering roles in both Pharmaceutical and Biologic businesses.
Proven proficiency in technical science writing, specifically in regard to chemical monographs for risk assessment.
Experience in both occupational (e.g. worker exposure) and quality (e.g., patient safety) toxicology assessments.
Familiar with regulations and guidelines for both worker and patient safety
Applied, working knowledge of the general principles, practices, and procedures of multiple facets including pharmacology, toxicology, biology, and chemistry.
Excellent written and verbal communication skills as well as proven negotiation, collaboration, and interpersonal leadership skills.
Significant experience in people management and networking in a matrix organization.
Ability to influence strategically and persuade tactfully, to obtain desired outcomes while maintaining effective organizational relationships.
Good appreciation of SHE processes and policies, with senior management, consultancy or advisory experience in influencing strategy.

Nice To Haves

PhD in toxicology or related biomedical science field.
Familiarity with the latest research and thinking in specialist areas.
Professional Business Qualification/Certifications

Responsibilities

Lead a team of global experts supporting the business with problem-solving in all aspects of occupational toxicology and hazard/risk assessments.
Oversee the AZ Global Panel for OEL/PDE to ensure the achievement of near-term deliverables and strategy to meet long-term business demands.
Establish health-based exposure limits and author documentation for regulatory compliance, including Permitted Daily Exposures (PDEs) to support product quality and worker health and safety activities.
Provide toxicology support for nonclinical safety assessment groups with requests from project teams, development, and toxicology leads.
Prepare toxicology assessments in support of health hazard classification for Safety Data Sheets according to GHS and CLP, and Dangerous Goods to support worker safety as well as general public in support of chemical notification/registration.
Implement robust risk management processes to support health hazard assessment for employees handling proprietary and non-proprietary chemicals used in the production of medicinal products.
Manage occupational testing programs in compliance with evolving global and company regulations and guidance.
Provide technical and scientific support for setting limits for releases into the aquatic environment.
Maintain toxicological expertise relevant to nonclinical safety of drugs, occupational health, and product quality risk.

Benefits

Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

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