What are the responsibilities and job description for the Senior Director, Drug Product and Packaging Tech Transfer position at AstraZeneca?
Location: Gaithersburg
Be a Catalyst for Change at AstraZeneca
Are you ready to lead with purpose and drive innovation that makes a global impact? Join AstraZeneca as our Senior Director, Drug Product and Packaging Tech Transfer, and play a vital role in delivering life-changing medicines to patients worldwide.
As part of our Global Technical Operations team, this leadership role puts you at the forefront of technological advancements, where you’ll shape cutting-edge solutions across modalities like biologics, vaccines, and combination products. Collaborating with a diverse network of experts, you’ll ensure the seamless validation and delivery of transformative therapies while building robust global supply chains.
Why Join Us?
At AstraZeneca, we’re united by a shared purpose: to push the boundaries of science to deliver medicines that transform lives. This role offers the opportunity to lead a world-class team, work on pioneering projects, and contribute to a culture of innovation, inclusivity, and collaboration.
Your Role at a Glance
As a key member of the Tech Transfer & Validation Leadership Team, you’ll bring vision and strategy to our technical projects. You will lead and inspire a team of subject-matter experts, collaborate across global functions, and champion advancements in sustainability, modernization, and operational excellence.
Key Responsibilities
Team Leadership
Essential Skills and Experience
Be a Catalyst for Change at AstraZeneca
Are you ready to lead with purpose and drive innovation that makes a global impact? Join AstraZeneca as our Senior Director, Drug Product and Packaging Tech Transfer, and play a vital role in delivering life-changing medicines to patients worldwide.
As part of our Global Technical Operations team, this leadership role puts you at the forefront of technological advancements, where you’ll shape cutting-edge solutions across modalities like biologics, vaccines, and combination products. Collaborating with a diverse network of experts, you’ll ensure the seamless validation and delivery of transformative therapies while building robust global supply chains.
Why Join Us?
At AstraZeneca, we’re united by a shared purpose: to push the boundaries of science to deliver medicines that transform lives. This role offers the opportunity to lead a world-class team, work on pioneering projects, and contribute to a culture of innovation, inclusivity, and collaboration.
Your Role at a Glance
As a key member of the Tech Transfer & Validation Leadership Team, you’ll bring vision and strategy to our technical projects. You will lead and inspire a team of subject-matter experts, collaborate across global functions, and champion advancements in sustainability, modernization, and operational excellence.
Key Responsibilities
Team Leadership
- Lead, mentor, and manage a team of 6–8 technical experts responsible for:
- Overseeing commercial drug product tech transfer projects across internal and external sites within the global AstraZeneca network.
- Driving validation activities including process validation, fill-finish, and shipping qualification for biologics drug product intermediates and finished goods.
- Foster a culture of innovation and continuous improvement by identifying opportunities to enhance technical and operational excellence.
- Leverage lean methodologies and risk-based approaches to optimize processes and deliver cutting-edge solutions.
- Champion digital transformation initiatives and collaborate across technical, quality, and leadership teams to implement innovative strategies.
- Partner with design and engineering teams to develop a vision for sustainable packaging and shipping qualification practices that align with both environmental and business goals.
- Lead multi-disciplinary teams to establish and implement global best practices, guidelines, and training for tech transfer and validation processes.
- Drive modernization efforts by authoring and updating procedures, incorporating state-of-the-art approaches, and streamlining processes using lean, risk-based methodologies.
- Establish priorities for Business Process Management, including:
- Developing standardized “blueprints” for operational workflows.
- Creating “playbooks” to align practices across global teams.
Essential Skills and Experience
- Education:
- Bachelor’s degree in engineering or a related field with 15 years of relevant experience (graduate degree preferred).
- Technical Expertise: Proficiency in at least three of the following areas:
- Large Molecule/Biologics drug product topics from development to GMP operations, including parenteral fill-finish, aseptic processing, lyophilization, and packaging.
- Drug product transfer and validation/qualification processes, including packaging and fill-finish equipment.
- Regulatory requirements and industry best practices for biologics drug product development, tech transfer, and supply chain establishment.
- Business process excellence and operational optimization.
- Industry Experience:
- Extensive experience within GMP development, logistics, scale-up, and/or manufacturing in the biopharma industry.
- Regulatory Knowledge:
- Strong understanding of global validation life-cycle activities and compliance with regulatory and GDP standards.
- Leadership & Collaboration:
- Demonstrated ability to lead diverse, cross-functional teams and inspire innovation in a global, matrixed environment.
- Exceptional interpersonal skills, with the ability to influence and build consensus across teams.
- Advanced degree (PhD strongly preferred).
- Experience with new modalities (e.g., ADCs, radioconjugates, cell therapies).
- Familiarity with digital transformation tools (e.g., process modeling, product lifecycle management, data visualization).
- Certification or experience in Lean, Six Sigma, or Project/Portfolio Management.
- Expertise in temperature-controlled transport and logistics qualification.
Salary : $179,000 - $269,000