Director of Analytical Development

2 days ago

East Kilbride, South Lanarkshire, United Kingdom Ferring Holding SA Full time
Head of Analytical Development

At Ferring, we seek a highly skilled and experienced leader to head our analytical development team. As our new Head of Analytical Development, you will be responsible for strategically strengthening the area of analytical method development, validation, chemical characterisation, stability and controls with a focus on controlled release Drug Products.

You will lead a team of highly skilled scientists, planning, coordinating, leading and evaluating analytical development and characterisation work performed in our internal laboratories and at different CROs. Your primary tasks will include:

  • Leading, motivating and developing your team via daily coaching, problem solving, individual objectives and performance reviews
  • Ensuring the definition and delivery of robust analytical packages to support drug development projects
  • Building a thorough understanding of Ferring's value chain and global organization
  • Building and maintaining constructive relations to a wide number of stakeholders in the global organization
  • Building an external network to relevant experts and across the scientific community
Leadership Profile

We are looking for a genuine enabler who can drive things forward without having a detailed manual in place. If you are the one who finds great satisfaction in helping other people to be their very best, we want to hear from you. You will have the scientific knowledge to engage with a team of experienced Scientists but are not necessarily a scientific specialist yourself. Instead, your professional interest is driven by motivating people and making things better.

Your CV should comprise:

  • A degree in chemistry, pharmacy or equivalent
  • 15+ years of experience with delivering CMC projects in the pharmaceutical industry
  • Technical understanding of drug product analytical development, including method development and validation, stability and controls
  • Sound knowledge of ICH and other regulatory guidelines including quality by design
  • Ideally experience with both large and small molecules and expertise within polymer chemistry
  • Drug product development project management
  • Experience of all phases of analytical development and understanding of global regulatory requirements for CMC to ensure high quality regulatory submissions
  • Leadership experience of teams consisting of senior scientists and scientists to drive decision making within cross functional teams
  • Fluency in English, written and spoken

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