Introduction
Join AstraZeneca Biologics as a Process Engineering & Packaging Leader and drive innovation in biopharmaceutical process development and technology transfer across our UK and EU operations.
Accountabilities
Lead the UK/EU team responsible for process development and packaging for clinical products. Oversee process development for diverse biopharmaceutical dosage forms, including liquid and lyophilized formulations, primary container formats, novel drug delivery formulations, devices and packaging. Maintain strong technical culture and build relationships at internal and external interfaces.
Responsibilities
- Provide technical and strategic leadership for drug product and device assembly processes, covering design for manufacturability, clinical and commercial fill‑finish development, clinical packaging, technology transfer and ad‑hoc technical support.
- Apply scientific and engineering knowledge to resolve issues during development and execution of manufacturing processes.
- Lead and manage a team of 8‑10 scientists and engineers, including resource management, prioritisation, technical assessment, and partnership with functional teams.
- Mentor and develop high‑performing teams, building the next generation of technical leaders.
- Create strategies to evolve organisational capabilities in line with AstraZeneca Biologics strategies and changing external drug product landscape.
- Drive a culture of innovation and high‑quality science and engineering.
- Influence regulatory strategies and provide guidance on regulatory submissions.
- Represent BPD on senior leadership teams, committees and councils, including external engagement at conferences.
Essential Skills/Experience
- BSc, MSc, PhD or equivalent in Chemical Engineering, Pharmaceutics or closely related field.
- Proven experience in the biopharmaceutical industry.
- Deep technical foresight in development and optimisation of drug product manufacturing processes for biologics in primary containers and devices.
Leadership & Experience
- Industry leader in drug product manufacturing process development with progressive managerial experience leading technical teams.
- Expertise in delivering pivotal initiatives across diverse biopharmaceutical portfolios.
- Track record of leading enterprise‑level committees, critical initiatives and multi‑functional task forces.
Technical Expertise
- Design for manufacturability principles applied in biopharmaceutical production.
- Proficiency in Six Sigma and continuous improvement tools.
- Experience in CMC aspects from early‑stage through commercial production.
- Understanding of current industry scientific and technical advancements.
Regulatory & Stakeholder Management
- Extensive experience managing regulatory agency interactions and preparing technical submissions.
- Ability to influence senior organisational levels and engage executive leadership teams.
People Leadership & Development
- Capabilities in developing and inspiring professional staff across technical subject areas in collaborative, matrix environments.
- Expertise in building high‑performing, diverse teams that foster innovation and continuous learning.
- Collaborative approach working across technical functions and geographical locations.
Equal Employment Opportunity
Our mission is to build an inclusive and equitable environment. We welcome and consider applications from all qualified candidates, regardless of characteristics, and offer reasonable adjustments for candidates requiring accommodations.
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