Associate Principal Scientist - Macclesfield, United Kingdom - AstraZeneca
Description
Associate Principal Scientist (Analytical) Senior Project and Technical Lead
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceutical and the supply of healthcare services.
Here, employees are empowered to express diverse perspectives and are made to feel valued, energized and rewarded for their ideas and creativity.
Pharmaceutical Technology and Development (PT&D) are the bridge, which turns brilliant science into actual medicines that help millions of people.
We work across the entire value chain, designing and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
Introduction to role:
Join our multi-skilled On-Market support group within Chemical Development at AstraZeneca, dedicated to the lifecycle management of commercial active pharmaceutical ingredients (API).
As an experienced analytical scientist, you will lead our analytical technical contribution to maintain and optimise supply for one or more AstraZeneca commercial products.
This role is a unique opportunity to shape the future of Operations at AstraZeneca and contribute to delivering more medicines to patients, quicker and more affordably.
Accountabilities:
You will be responsible for leading the authoring and providing a significant contribution to the CMC components of regulatory submissions.
You will provide expert technical input to change control and improvement activities at CMOs and internal AZ API manufacturing sites.
You will represent Chemical Development as lead analyst on CMC Project delivery and Global Supply Teams. You will also coach and develop junior colleagues, supporting them in reaching their full potential.Essential Skills/Experience:
- BSc/PhD level education in a relevant discipline
- Significant experience working within a Research & Development and Manufacturing environment, within the pharmaceutical industry
- Good understanding of the overall drug development process from discovery through to launch
- Experience of technical supervision, coaching and mentoring or leading small teams of people or scientific projects
- Specialist in one or more related analytical areas or techniques
- Thorough understanding of the principles and management of SHE and cGMP
- Significant experience of delivering CMC content or contributions to regulatory filings throughout the life cycle of process or formulation analytical development, in the pharmaceutical industry
- Understanding of key analytical techniques, including NMR, chromatography and mass spectrometry
Skills/Experience:
- Ability to think and operate across functional boundaries
- Excellent communication and strategic influencing skills across interfaces of discipline, culture, and expertise both internally and externally
- Proven problem solver with indepth technical skills
- Proficiency in the use of statistics to understand data
- Experience of supporting commercial manufacture and working with contractors
- Experience of latestage development with a background in an analytical skill group
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