Scientist/ Associate Scientist Method Development - LCMS
Quick Summary
Responsible for developing and qualifying highly sensitive,
Minimum of a Bachelor’s degree in Biochemistry,
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
As an Associate Scientist / Scientist, Method Development, you will use scientific knowledge, literature, and creativity to develop rugged, robust, and scientifically innovative bioanalytical methods while contributing to building a collaborative and cohesive team that will exceed client expectations.
Responsibilities
~1 min read- →Responsible for developing and qualifying highly sensitive, reliable LCMS methods for the rapid and accurate analysis of compounds in biological matrices
- →Consult with clients on method development and validation needs and establish appropriate bioanalytical assays to meet client needs
- →Ability to work on projects of diverse scope that require non-routine analysis and evaluation of scientific data
- →Ability to work independently and on multiple projects simultaneously in an efficient manner
- →Interact with validation and production teams to provide efficient transfer of analytical methods and reagents post-development
- →Responsible for troubleshooting assays, as needed
- →Responsible for applying design of experiments (DOE) and other systematic and statistical approaches to method development
- →Ability to work in a collaborative team environment and communicate professionally
- →Mentor and provide scientific expertise to the method development team
Requirements
~1 min read- Minimum of a Bachelor’s degree in Biochemistry, Chemistry or Biology with 3-5+ years of related industry experience
- Strong knowledge of organic chemistry is preferred
- Strong problem-solving skills are required
- Prior experience working in a regulated GLP-compliant environment is preferred
- Experience developing LCMS assays in biological samples required; experience developing large molecule assays by LCMS is preferred
- The ability to design experiments with multiple variables, including appropriate positive/negative controls
- Knowledge of Laboratory Automation, Chromatographic/MS-MS Software (e.g., Analyst) and LIMS systems (e.g. Watson) preferred
- Experience with capillary electrophoresis, supercritical fluid chromatography (convergent chromatography), or GC-MS is a plus
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
Location & Eligibility
About this job
- Who can apply
- United States
- Posted
- 636 days ago
Listing Details
- Posted
- January 22, 2025
- First seen
- October 20, 2026
- Last seen
- October 21, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 29%
- Scored at
- October 21, 2026
Signal breakdown
Celerion is a leading Clinical Research Organization focused on accelerating early phase drug development through innovative strategies and comprehensive research services.
View company profileSimilar Other jobs
View all →Stay ahead of the market
Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.
No spam. Unsubscribe at any time.
