Detail

Salary
negotiable
Location
Macclesfield, UK
Posted by: Astra Zeneca
22 Dec
472 Views
20 Feb EXPIRED

Senior Scientist - Analytical Development Project Lead

Macclesfield, UK
Job Description

We are currently looking for lead analytical pharmaceutical development scientists in chemical development with scientific project-based experience. Join one of our Chemical Development teams within Pharmaceutical Technology and Development (PT&D), at our Macclesfield Campus, UK.

 

Pharmaceutical Technology and Development (PT&D) are the bridge, which turns forward-thinking 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.

 

You will join a vibrant team that is working on the next generation of medicines and play a key role in the analytical development of new medicinal products. We will rely on you to bring a strong analytical perspective to multi-disciplinary project teams and to help lead the early and late stage development of drug substances. You will be responsible for using science and innovation to deliver analytical knowledge that encompasses understanding of manufacturing processes, control strategy and robustness. We would like you to work independently and to lead interactions within cross functional teams, including with Process Chemists, Engineers, Contract Manufacturing Organisations (CMOs), Product Development, Regulatory CMC, Quality Assurance and Supply Chain.

 

As part of a global company with a focus on developing its people, you will have the opportunity to develop both personally and professionally while helping to deliver medicines that help millions of patients worldwide.

Job ID Reference
1448
Desired Skills & Experience

Main Duties and Responsibilities:

  • Leading API analytical activities to support project progression from clinical development phases through to late development and commercialisation

  • Developing API analytical control strategies, keeping a strong focus on quality for our patients

  • Identifying and solving potential analytical project issues

  • Planning and conducting lab-based experimental work in accordance with project timelines

  • Supporting the technical development of other scientists

  • Collaborating with internal and external manufacturing partners to deliver the analytical aspects of GMP API manufacture

  • Keeping abreast of scientific developments and proactively applying existing and novel approaches to projects

  • Authoring the CMC components of regulatory submissions and preparation of successful regulatory responses

 

Required Qualifications, Skills, Knowledge and Experience:

  • A degree (BSc, MSc or equivalent) in Chemistry or Analytical Chemistry with a proven track record of analytical development in a pharmaceutical environment, or a PhD including aspects of analytical measurement

  • Knowledge and practical experience across a range of analytical techniques, e.g. LC, MS, GC, NMR

  • Scientific leadership skills and the ability to use knowledge and experience to assess options available and deliver robust scientific contributions to projects

  • Strong problem-solving skills, underpinned by strong practical laboratory experience

  • Experience of working collaboratively within a mixed skill technical team, and ability to develop and utilise networks

  • Ability to communicate complex scientific information in a clear, concise and understandable way

 

Desirable Skills, Knowledge and Experience:

  • Ability to confidently and successfully lead improvement projects

  • Strong influencing, planning and prioritisation skills to ensure project delivery to deadlines

  • Experience of leading technical teams, coaching and people development

  • Commitment to improvement and innovation and knowledge of Lean principles

  • Knowledge and practical experience of quality and regulatory requirements (GMP and ICH) and health and safety requirements

Company
  Cheshire, Macclesfield, UK
  www.astrazeneca.com
AstraZeneca is an exciting global, innovation-driven biopharmaceutical company. We’re inspired by what science can do. Driven by the desire to meet unmet patient needs in our core therapeutic areas. Bold in our thinking. Proactive in pursuing discoveries beyond imagination. At sites across the world, we bring teams together in a spirit of collaboration to turn great ideas into life-changing medicines – strengthening our product portfolio and harnessing the potential of a pipeline across all stages of the drug development process.
You’ll be part of a team that’s rolling back the frontiers of science to turn yesterday’s impossible into the normal of tomorrow. So, if you share our focus and passion, join us and make a difference to patients – and in return, we’ll help you develop way beyond what you thought possible.
  Workplace
 Macclesfield, UK