Full-Time Analytical Technology Transfer Scientist

This is a full-time, permanent position working a 36.5 hour week, Monday - Friday 08:00 - 16:30. This role is homebased within the UK but we would consider overseas applicants.

Opportunity for an Analytical Scientist: This is a new and exciting opportunity based at our client's facility, a world-class Pharmaceutical company based in Macclesfield. We have an opportunity for an experienced Analytical Scientist with experience of drug product analytical development in the pharmaceutical industry.

Responsibilities: The role will involve being the responsible point of contact for a major commercial product or group of products related to the analytical testing subject matter area. Using your expertise in Analytical Chemistry you will support the client's manufacturing sites and CMOs to ensure performance, robustness and compliance of OSD products and related analytical methods. You will support major changes and market access projects in collaboration with multiple functions (External Sourcing and Manufacturing, Quality Assurance, Quality Control, Regulatory Affairs, Manufacturing) Transfer of commercial analytical methods to multiple locations and may involve international travel.

Potential Support: Potential support in practical analytical activities.

Qualifications: Degree, Master's degree or PhD level with experience post-degree in an appropriate discipline such as Chemistry, Pharmacy, Pharmaceutical Sciences or similar discipline. Good understanding of OSD, Inhalation and Parenteral drug products life-cycle from late stage development to launch and through the commercial life cycle. Good knowledge of analytical methods establishment, optimisation and transfer for release and stability testing. Understanding of a broad range of Analytical techniques (standard and non-standard) Good experience on issue investigation and change assessment from an analytical point of view. Good knowledge of standard tools for root cause analysis. A thorough understanding of principles, applications and management of SHE and cGMP. Good communication and leadership with demonstration of being able to work across different functions. Experience in or exposure to multiple disciplines in CMC and related functions (e.g. Product Development, Product Manufacturing and testing, Quality Assurance, Regulatory) would be desirable. Previous experience and training in Lean methodologies would also be desirable.

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