Analytical Scientist

Analytical Scientist

Eurofins

Sittingbourne, United Kingdom

Job Description

The purpose of this job within Analytical Science is to support the client in both Manufacturing and R&D efforts by conducting analysis and characterization of the samples generated.

Please note this is a 6 month fixed term contract.

• Support formulation development through hands-on generation of accurate and precise analytical chemistry data using routine laboratory techniques.
• Design and execution of studies to ascertain degradation mechanisms in the solution and solid state.
• Assess stability risks by evaluating process changes and impact on degradation chemistry or dissolution profile.
• Development of assay/purity methods and assessment of method robustness/ruggedness.
• Development and execution of method validation protocols.
• Transfer of analytical methods to other laboratories and remote sites.
• Hands-on generation of data in support of accelerated and registration stability studies.
• Development and support of Process Analytical Technology (PAT) techniques.
• Demonstrate understanding of root cause analysis methodologies and be able to support investigations as required.
• Demonstrate an understanding in the analyses required in the formulation of amorphous dispersions.
• Report and communicate project outcomes in an appropriate manner.
• Identify and resolve promptly any problems occurring at any phase of a study, escalating to the line manager where necessary.
• Ensure all applicable quality measures are met and adhered to.
• To keep an accurate up to date laboratory notebook including interpretation or results, conclusions and next steps.
• To collect and measure productivity through agreed metrics such as the number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc.
• Ensure that the client gets the best possible service by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards.
• To become fully familiar with and keep up to date with any technological or method revisions in their area.
• To keep the laboratory area clean and tidy in both ‘seen’ and ‘unseen’ areas.
• To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards.
• To update any relevant documentation when requested.

Qualifications

• A degree in Chemistry or a related discipline is required.
• A sound, fundamental knowledge and practical application of Organic Chemistry to pharmaceutical drug design is essential.
• Appropriate relevant experience of Analytical Science and analytical tools and techniques within a group organisation.
• Good foundation and experience with traditional analytical techniques as well as modern instrumental equipment (e.g., HPLC/UPLC, NMR (liquid), mass spectrometry, vibrational spectroscopy, USP/EP dissolution, Karl Fischer titration). Must possess sound knowledge of analysis methods and tools.
• Ability to quickly learn new processes.
• Ability to work using fully electronic media, including MS Office.
• Ability to communicate clearly and to form strong working relationships with colleagues.
• Ability to work in a laboratory environment with some supervision and be capable of developing solutions to problems as part of a team.
• Willing to operate in a flexible manner and able to reuse both internal and external experiences and incorporate them into relevant improvements. Ability to switch priorities at short notice is desired.
• Good team player, organised, accurate, have strong documentation skills.
• Passionate about quality and client service.
• Good communication skills both internally and externally and avoids making mistakes that will hinder the understanding of his/her written and verbal exchanges.

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