Senior Scientist – Analytical Sciences, inhalation

Are you an experienced scientist looking for a role where your expertise can make an outstanding impact? Can you envision joining a dynamic and enthusiastic environment, delivering critical support to commercial products and market access projects? Then join us in this exciting opportunity!

AstraZeneca is a global, innovative BioPharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious disease. 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. Always committed to lifelong learning, growth and development.

We have an exciting opportunity to join as a Senior Scientist - Analytical Sciences in the Analytical Science & Technology CoE! In this role you will work within Technical Operations, Science and Innovation (TOSI), a key function of our Pharmaceutical Technology & Development (PT&D) organization.

The PT&D Organization is responsible for drug product design, development and technical support for drug substance and products throughout the lifecycle. TOSI is a multi-skilled global organization based in 13 locations in 7 countries, which provide technical leadership and subject matter expert support to AstraZeneca commercial small molecule drug products. Our technical support and expertise spans across formulation, process engineering, analytical, statistics, devices, packaging and process intelligence. The areas in which we deploy our technical expertise are in the support of drug product improvement projects, changes, technology transfers, investigations, product launches and regulatory submissions, product robustness, validation and risk evaluation.

What you’ll do

As Senior Scientist - Analytical Sciences, you will be responsible to provide analytical support to a portfolio of inhalation products (pMDIs) across their commercial lifecycle. Using your knowledge in analytical science and analytical technologies, you will provide expertise and leadership to ensure efficient and effective support to internal and external manufacturing sites located in multiple countries.

Your main accountabilities will include:

Being a key analytical contact for drug products and supporting all analytical lifecycle activities to ensure testing methods, specifications and control strategies are and remain fit for purpose and aligned with technology advancements.

Working in multi-functional cross-site teams supporting analytical technology transfer projects to internal and external manufacturing and testing sites.

Assessing technical changes and playing a proactive role in identifying opportunities for analytical method improvements, including automation.

Providing analytical subject matter expertise in support of issues investigations in QC laboratories and manufacturing sites.

Performing laboratory work, when needed to support projects and products.

Providing SME support during the regulatory file authoring and the interaction with local authorities for regulatory submissions, variations, and license renewals.

Supporting analytical risk assessments related to nitrosamines, extractables & leachables, elemental and organic impurities.

Providing technical support to Issue Management Team (IMT).

Supporting the definition of analytical standards impacting commercial products, specific to regulatory expectations and good business or quality standards (including pharmacopeial standards).

Essential requirements

MSc or PhD degree, complemented with considerable experience in an appropriate subject area such as Analytical Chemistry, Pharmacy, Pharmaceutical Sciences or similar.

Strong technical knowledge, great interpersonal skills and proven track record to lead and collaborate across teams, functions and locations.

A good understanding of the overall drug development and commercialization process from development, launch and through life cycle management

In-depth understanding of analytical sciences in the Pharmaceutical Industry applied to inhalation products, including raw materials and intermediates. Good understanding of control strategies and specification setting, analytical method's validation, transfer and optimization and proven knowledge of a broad range of analytical techniques.

Experience of issue investigation and change assessment from analytical point of view. Good knowledge of standard tools for root cause analysis (5 whys, PPS, Level 0, etc.)

A thorough understanding of principles, applications and management of SHE and cGMP.

Fluency in English, both spoken and written

Desired for the role

Experience in or exposure to multiple subject areas in CMC and related functions (e.g. product development, on-market support, manufacturing and testing)

Previous experience and training in Lean, problem solving tools and experience in data analysis and interpretation

Why AstraZeneca

Join our global team to experience our inclusive and encouraging culture. We believe in shared success, a place where ideas are welcomed and awarded. Be comfortable speaking up, taking responsibility for your actions and working together to succeed. This is the place to make an impact. Here we ensure everyone can reach their full potential, perform at their best and make a valued contribution to the enterprise.

So, what’s next!

We welcome your application no later than September 20th, 2023 .

Competitive salary and benefits package on offer.

• Opening date: August 25th, 2023
• Closing date: September 20th, 2023

Date Posted

25-aug.-2023

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.