Chemical Development Trace Analysis Scientist

Unfortunately, we are unable to offer visa sponsorship for this role.
This is a full time, permanent position, working a flexible 36.5 hour week, Monday – Friday.
We are currently recruiting for an enthusiastic and innovative Analytical Scientist. This is an exciting opportunity based at our client’s facility, a world class Pharmaceutical company based in Macclesfield. We have an opportunity for experienced Analytical Scientists with experience of drug substance development in the pharmaceutical industry.
Job Responsibilities that you be covering:
You will develop, optimise and validate advanced trace analysis methods using LC-MS and Orbitrap technologies to detect and quantify trace-level small molecules in raw materials, intermediates and drug substances.
You will provide technical expertise to Eurofins project teams, supporting the assessment of mutagenic impurities, nitrosamines and other trace analytes at parts-per-billion levels.
You will perform complex analytical investigations, interpret scientific data and apply innovative problem-solving skills to deliver accurate, high-quality results for clients.
You will support and enhance Eurofins' trace analysis capabilities by sharing specialist knowledge, advising stakeholders and contributing to the successful delivery of analytical programmes.
You will author and review key analytical documentation, including analytical testing plans, method development reports and validation protocols, depending on your level of experience.
You will collaborate effectively with multidisciplinary internal and external teams, communicating scientific concepts clearly while contributing to a culture of technical excellence, continuous improvement and professional development.
What skills, qualifications and experiences you will hold as an Chemical Development Trace Analysis Scientist:
You will hold a degree or higher qualification in Chemistry, Analytical Chemistry or a related scientific discipline, supported by a strong foundation in organic chemistry and analytical science.
You will have pharmaceutical analytical experience within a development laboratory environment, with knowledge of drug development processes and the analysis of raw materials, intermediates and drug substances.
You will have hands-on experience developing and applying advanced analytical techniques, including LC-MS/MS, GC-MS/MS, GC-HRMS and LC-HRMS, with experience of NMR, IC or ICP-MS considered advantageous.
You will have strong troubleshooting and problem-solving skills, with the ability to investigate analytical and instrumentation issues, quickly learn new processes and develop effective technical solutions.
You will have a good understanding of GMP requirements and experience working with electronic systems and Microsoft Office, alongside excellent documentation, organisational and data management skills.
You will have excellent communication and relationship-building skills, with the ability to work independently and collaboratively, adapt to changing priorities and demonstrate a strong commitment to quality, customer service and continuous improvement within Eurofins.

Employment type
Full-time

Work arrangement
No