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Given our continued success, we are actively seeking a Senior Analyst to join our growing Bioanalytical LC-MS/MS team in Manchester.
Given our continued success, we are actively seeking a Senior Analyst to join our growing Bioanalytical LC-MS/MS team in Manchester.
This is an exciting opportunity to apply your quantitative LC-MS/MS experience within a GLP, GCP and GMP-accredited laboratory.
You'll prepare, run and process clinical and non-clinical samples while supporting long-term pharmaceutical and biopharmaceutical client programmes.
If you're an experienced LC-MS/MS analyst who values quality, teamwork and continued development, we'd love to hear from you.
The position requires a practical and quality-focused Senior Analyst with hands-on quantitative LC-MS/MS experience and the confidence to work with clinical samples in a regulated laboratory.
You'll have approximately two to three years of relevant industry experience and be comfortable preparing, running and processing samples.
Bioanalytical and pharmacokinetic experience is highly desirable, although strong quantitative LC-MS/MS experience is the essential requirement.
You'll join a close-knit team where colleagues work collaboratively, support one another and share their knowledge.
You'll receive structured training in our processes, instruments and software before progressing to independent and more complex work.
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As a Senior Analyst, you'll perform quantitative LC-MS/MS analysis supporting pharmaceutical and bioanalytical studies.
You'll work with clinical and non-clinical samples and may analyse small and large molecules such as pharmaceuticals, proteins, peptides, lipids and oligonucleotides.
Your first few weeks will involve structured training and shadowing while you become familiar with our laboratory systems and quality processes.
You'll receive support on our instruments and software, including relevant supplier training modules, before beginning with batch analysis and moving into more complex work as your confidence grows.
This role combines the security of established methods with the opportunity to develop broader technical capability.
Depending on your experience, you'll also contribute to method development and validation while working across a varied portfolio of client projects.
This is an excellent opportunity to continue developing your bioanalytical career within a global pharmaceutical testing organisation and a supportive, experienced team.
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Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues.
We are a global family that values diversity and we thrive working together with precision, pace, and passion.
We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
We are an Equal Opportunity Employer who do not discriminate against applicants.
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies
Intertek is a global provider of assurance, testing, inspection, and certification services. It helps organizations assess quality, safety, sustainability, and regulatory compliance across products, operations, and supply chains.
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