Associate Director / Director - Oral Solid Dosage

Macclesfield, UK or Gartuna, Sweden

Make a meaningful impact on people’s lives with life-changing medicines

Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale, we are committed to delivering at the highest quality. Here we turn molecules to medicines, bringing our Research & Development pipeline to life through a meticulous process of development, manufacturing, testing and delivery.

The PT&D Organization is responsible for drug product design, development and technical support for drug substance and products throughout the lifecycle.

We now have an exciting opportunity for an Associate Director / Director - Oral Solid Dosage to strengthen our team! In this role you will work within Technical Operations Science and Innovation (TOSI), a key function of our Pharmaceutical Technology & Development (PT&D) organization.

TOSI is a multi-skilled Global organization based in 13 locations in 7 countries who provide the expert technical support for AstraZeneca commercial small molecule drug products, product robustness, manufacturing technology strategy and Packaging Development & Technology.

Underpinning the excellent technical support that drives robust product supply are technical processes & strategies around knowledge management, manufacturability, technical validation approaches, problem solving in alignment with the delivery of the technical inputs needed for fulfilling the Global Product Supply Strategy. We work closely with many technical functions across Operations providing the ability to drive science and build capability within our organisation and our ways of working.

What you’ll do

Provide both strategic and operational leadership to a team of individuals who provide expert technical support for our oral solid dosage commercial products. The team will comprise skills such as pharmaceutics, engineering and statistics and will work in close collaboration with analytical and packaging.

Your team will support:

• AZ manufacturing sites and CMOs to ensure performance, robustness and compliance of OSD products and related manufacturing processes

• Major changes and market access projects in collaboration with multiple functions (Global external sourcing, Quality Assurance, Quality Control, Regulatory Affairs, Manufacturing)

• Play an important role in ensuring transfer of commercial products to multiple locations

You will have a significant impact on the overall success of Global Operations as well as ensuring the commercial viability of current products. The activities of the group help to ensure availability of all AstraZeneca products to the commercial organization.

Duties and responsibilities

Manage a team of up to 10 people, coaching direct reports for enhanced performance and individual development on an ongoing basis.

Lead the implementation of new practises that enable the group to achieve flexibility, efficiency and delivery.

Create and sustain a high quality and innovative function, to continuously improve in competence, technical excellence and innovation.

Ensure delivery of SHE and cGMP compliance, ensuring that all work is carried out with regards to AZ and external regulatory policies and standards.

Operate confidently as part of a global organisation with an integrating attitude to create an organisation prepare for future challenges and change.

Develop the strategy for the delivery of the on market portfolio with technical leaders and the Project and Portfolio Management group, with accountability for the technical strategy for the products within their area of responsibility.

Develop solutions to a diverse range of problems requiring complex judgements based on highly developed levels of conceptual thought and strategic vision analysis.

Excellent communicator, setting clear direction to motivate and engage all staff and to collaborate effectively with key partners e.g. between PT&D and the AZ sites/GES managed sites and Global Partners.

Essential Skills & Experience

• Educated to BSc or PhD level in an appropriate field (or equivalent)

• Experience relevant to the pharmaceutical industry and have professional credibility within the business and industry.

• Excellent understanding of the overall drug development and commercialisation process from development, launch and through life cycle management

• Broad understanding of the various scientific fields within on-market.

• Thorough understanding of principles, applications and management of SHE and cGMP.

• Experience in Operations and/or R&D with a track record of successful project leadership and delivery within a matrix organization.

• Excellent communication skills and the ability to build excellent relationships with customers/key partners

Preferred Skills & Experience

• Significant experience in the pharmaceutical industry

• Experience in or exposure to multiple fields in CMC and related functions (eg GPD, Operations, Global Supply, Marketing Companies)

• Strong eye for business and supply chain knowledge.

The successful individual will be appointed at either an Associate Director, or Director, level, dependent on experience.

Why AstraZeneca…

At AstraZeneca, we 're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.

So, what’s next?

Are you already imaging yourself joining our team? Good, because we can’t wait to hear from you!

We look forward to receiving your current CV and covering letter no later than Sunday 22nd January 2023.

Competitive Salary & Benefits

Open Date: 05.01.23

Close Date: 22.01.23

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Date Posted

Closing Date

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.