At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.
Position Summary
We are looking for an experienced and strategic Senior Director of Clinical Site Supply Chain to lead and improve our clinical site supply chain operations in a the latest cell therapy environment. You will have a background in managing complex supply chains, with a focus on clinical manufacturing processes and compliance with regulatory requirements. You will manage the supply chain teams at four (4) clinical manufacturing sites located in Santa Monica CA, Los Angeles (Tarzana) CA, and Gaithersburg MD. This role is important to ensure the seamless production and delivery of cell therapy products and driving supply chain excellence. The Senior Director will report directly to the VP of Supply Chain.
Responsibilities:
- Develop supply chain strategies for cell therapy manufacturing sites that align with our clinical and operational goals.
- Identify solutions to enhance supply chain processes, including planning, warehouse and inventory management, logistics, procurement, to support our growth goals, improve efficiency and reduce costs.
- Improve programs across the clinical supply chain, focusing on reducing lead times, optimizing inventory and capacity levels, and improving overall efficiency.
- Develop manufacturing site capacity plans.
- Oversee end-to-end clinical supply chain operations, including supply and capacity planning, scheduling, production order management, materials delivery and inventory control, and delivery of patient material.
- Address risks and develop contingency plans and strategies to address potential disruptions in the supply chain.
- Ensure the efficient delivery of clinical trial materials, addressing any supply chain challenges that arise.
- Allocate resources to meet the dynamic needs of the clinical supply chain, including staffing, technology, and infrastructure.
- Work with Development, Manufacturing, Quality, and Global Supply Chain teams to coordinate supply chain activities that support clinical trials and product development.
- Implement industry best practices to maintain compliance with cGMP, FDA, and other regulatory requirements.
- Ensure that all supply chain processes meet the highest standards of quality and safety.
- Develop a supply chain team, encouraging a culture of collaboration, accountability, and continuous improvement.
- Provide guidance to team members, setting clear goals and performance goals.
- Manage the supply chain budget, ensuring cost-effective operations while meeting quality and service requirements.
- Conduct financial analyses to support strategic decision-making and cost-saving initiatives.
Requirements:
- Bachelor's degree in Life Sciences, Engineering, Supply Chain Management, or a related field; advanced degree (MS/MA, MBA, or PhD).
- 15+ years of experience in supply chain management, with a focus on clinical operations in the biopharmaceutical industry.
- Experience managing supply chains for cell therapy products.
- Experience leading supply chain teams in a regulated environment.
- Experience with clinical supply chain operations and managing supply chains for biopharmaceutical products in cell therapy.
- Knowledge of cGMP, FDA regulations, and other relevant regulatory requirements for clinical supply chains.
- Experience leading and developing teams.
- Guide and influence decision-making at the senior level.
- Resolve complex supply chain challenges and develop solutions.
- Proficiency in data analysis and the use of supply chain management tools and software.
The anticipated salary range for candidates who will work in Santa Monica, CA is $166,163 to $207,704. The final salary offered to a successful candidate is dependent on several factors that may include but are not limited to the type and length of experience within the job type and length of experience within the industry, education.
At Neogene we celebrate the diversity of our employees and our leadership. Neogene is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
DE&I Statement
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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