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Salary
$106k – $221k per year (Estimated)
Location
In office (Sweden)
Seniority
Staff · 5+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
AstraZeneca is a British-Swedish pharmaceutical company formed in 1999 by the merger of Astra of Sweden and Zeneca of the United Kingdom, and now one of the largest drug makers in the world by revenue. Its portfolio is concentrated in oncology with Tagrisso, Imfinzi and Enhertu, alongside cardiovascular, renal and metabolic products including Farxiga, respiratory and immunology medicines, and a rare disease business built on the acquisition of Alexion. Headquartered in Cambridge in England and listed in London, Stockholm and New York, it reports in United States dollars.

Are you ready to lead complex, global technology transfers that make a real difference to patients? As Associate Director, Packaging Tech Transfer Lead, you will drive the transfer of packaging technologies across AstraZeneca's diverse product portfolio, working with pioneering products and cross-functional teams around the world. This is a unique opportunity to influence strategic decisions, shape future ways of working, and deliver medicines safely and reliably to patients!

You will provide both strategic direction and hands-on leadership for the transfer of labelling, packaging, and device assembly processes across AstraZeneca’s internal manufacturing network and external manufacturing partners. You will work across development, transfer, launch, and lifecycle management activities, ensuring that transfers are delivered safely, compliantly, efficiently, and in line with Global CMC priorities.

Your role and accountabilities

In this role, you will:

  • Lead packaging technology transfers for vials, APFS, and autoinjector presentations across internal and external manufacturing sites.
  • Own end-to-end transfer activities, including labelling, secondary packaging, device assembly, documentation, readiness, and implementation.
  • Assess site capabilities and readiness, including equipment, process fit, capacity, technical maturity, materials, and operational risks.
  • Develop robust transfer plans in collaboration with Technical Operations, Manufacturing, Quality, Supply Chain, Regulatory, Device teams, Drug Product, Engineering, and external partners.
  • Ensure GMP and regulatory compliance by embedding quality, risk management, and inspection readiness into transfer activities.
  • Provide oversight of packaging process readiness, including line readiness, process validation considerations, comparability, material readiness, and transfer documentation.
  • Support device and combination product transfers, considering the interfaces between the primary container, device components, assembly operations, packaging configuration, and market requirements.
  • Consider drug product requirements and their impact on packaging configuration, handling, process conditions, product protection, and transfer strategy.
  • Contribute to shipping qualification and distribution readiness, including transport validation, distribution conditions, and product protection requirements.
  • Lead risk and issue management by identifying critical risks, defining mitigation plans, and calling out decisions when needed.
  • Influence strategic decisions related to transfer approach, site selection, execution priorities, and risk management.
  • Drive continuous improvement by simplifying, standardising, and improving packaging transfer processes, governance, and ways of working.
  • Champion digital enablement, including the use of Digital TT and other digital tools to improve visibility, data quality, knowledge management, and execution efficiency.
  • Lead through a matrix organisation, creating clarity, aligning stakeholders, and maintaining momentum across functions, sites, countries, and external partners.

Essential requirements

You will bring:

  • Significant experience (typically 5-10 years) within CMC, pharmaceutical packaging, technology transfer, manufacturing science and technology, technical operations, or a related field, supported by a Bachelor's or equivalent in a relevant scientific or engineering field.
  • Proven experience leading packaging technology transfers involving vials, APFS, autoinjectors, or similar presentations, with a strong understanding of labelling and packaging operations, device assembly where applicable, and associated transfer requirements.
  • Strong technical knowledge of GMP, quality systems, regulatory expectations, and manufacturing environments, including line readiness, validation, change control, process performance, material flows, and operational risk management.
  • Experience assessing manufacturing site capabilities and readiness, including technical fit, operational capacity, execution risk, and the successful planning and delivery of manufacturing transfers.
  • A solid understanding of drug product considerations relevant to packaging transfers, including the relationship between formulation, primary packaging, process conditions, product protection, shipping qualification, and distribution requirements.
  • Demonstrated leadership, influencing, and communication skills, with the ability to lead through ambiguity, engage stakeholders without direct authority, and explain complex topics to both technical and non-technical audiences.
  • Strong collaboration skills and experience working across functions, cultures, geographies, and organisational boundaries to deliver business outcomes.
  • An improvement attitude with the ability to simplify processes, develop scalable ways of working, and embrace digital tools and digital ways of working, particularly Digital TT.

Desirable requirements

  • Experience with combination products, biologics packaging, or other complex pharmaceutical product environments, including device-related manufacturing and assembly operations.
  • Experience leading transfers across internal manufacturing sites and external contract manufacturing organisations, supporting global supply networks, product launches, and lifecycle change management.
  • Experience working with Global CMC teams and translating CMC priorities into practical transfer plans, supported by experience using digital technology transfer tools or similar systems to manage transfer activities, data, actions, and documentation.

Why AstraZeneca

We're driven by our commitment to deliver accelerated growth and to make people's lives better. We're always working towards our ambition to deliver more medicines to patients quicker and more affordably. If you have the passion and the strive to accelerate growth and make people's lives better, then this is the place for you

What’s next

Own the transfers that keep medicines on shelves and launches on time-send your CV to lead the next wave of digital, data-driven tech transfer excellence.

Welcome with your application, no later than 20th of September. Interviews will be held continuously so don’t hesitate to apply!

Date Posted

09-sep.-2026

Closing Date

20-sep.-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
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