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Scientist 1 Bioanalysis/LCMS
Frontage Laboratories
Fordham, GBR
Full-time
Entry
Onsite
Discovered 3 days ago
LC-MS/MSmass spectrometrychromatographyGLPGxP
Free
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LC-MS/MSmass spectrometrychromatography
Role Overview
Why join us?
At Resolian, we're passionate about advancing scientific discovery and improving lives through the work we do. Our people are at the heart of our success, and we're committed to creating an environment where talented individuals can thrive, grow, and make a meaningful impact.
Joining Resolian means becoming part of a global organisation that values collaboration, innovation, and continuous improvement. We foster a culture where new ideas are welcomed, achievements are recognised, and professional development is encouraged. Whether you're leading critical projects, driving service improvements, or developing your expertise, you'll have the support and autonomy needed to make a real difference.
Alongside exciting work, a collaborative culture and opportunities for development, we offer a range of benefits designed to support your wellbeing, career growth and work-life balance.
Want to learn more about what it's like to work at Resolian?
Click here to explore our Life at Resolian page to discover our benefits, culture and employee experience.
Key Skills for This Role
LC-MS/MSmass spectrometrychromatographyGLPGxP
Full Job Posting
Description
As a Scientist 1 – Bioanalysis LCMS, you will support the development, validation, and application of LC-MS/MS methods for the quantitation of drugs and biomarkers, contributing to the analysis of biological samples from pre-clinical toxicology and clinical safety studies.
Working closely as part of a team, you will play an active role in planning your work, managing your time to deliver high-quality data to our customers, and maintaining accurate records in compliance with GLP.
What will you be doing?
• Develop and validate LC-MS/MS methods for the quantitation of drugs and biomarkers.
• Apply these methods to the routine analysis of biological samples from pre-clinical toxicology and clinical safety studies.
• Maintain thorough record keeping in compliance with GLP.
• Prepare study plans and reports.
• Plan and manage your own workload to ensure timely delivery of data to our customers.
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