Job Details
Posted 2 July, 2026
Job Id: 629049
Scientist- LCMS
Job Description
You will be responsible for assigned nonclinical bioanalytical studies method development, validation, sample analysis utilizing high performance liquid chromatography. You will also be responsible for direct interaction with clients, report writing, and adherence to regulatory guidelines. You will collaborate with other scientists, analysts, and departments in a team-oriented environment. You will possess knowledge and experience in a Good Laboratory Practice (GLP) environment and be able to adhere to GLP guidelines and practices.
What You’ll Do Here
- Serve as principal investigator or contributing scientist for LC-MS studies.
- Maintain open and direct communication and attend recurring calls with clients.
- Prepare all necessary driving documents for in-lab analysis.
- Complete and deliver scientific reports to clients on time.
- Collaborate with internal regulatory departments to ensure quality and compliance oversight on GLP studies.
- Prepare materials, including animal blood and tissues, for LC-MS assays and perform the assays according to Protocol or other guiding documents with accurate documentation.
- Maintain and document chain of custody for specimens, reagents, controls, and samples in the laboratory.
- Maintain and update facility records related to the laboratory and its analyses.
- Review laboratory records, procedures and study data for completeness and accuracy.
- Document deviations to laboratory procedures and study protocols and unforeseen circumstances in a timely manner and provide input for corrective actions.
- Assist in calibration, optimization, maintenance, and collection of data from analytical instruments.
- Follow Alta’s Standard Operating Procedures (SOPs), ensure compliance with GLP, ALCOA++, USDA, and AAALAC guidelines, and can identify areas for improvement.
- Perform routine laboratory maintenance (including cleaning, stocking supplies, equipment maintenance tasks, etc.).
What You’ll Need to Succeed
- Associates/Bachelor’s degree in Chemistry/Immunology/Biology or equivalent in discipline plus a minimum of 3 years of relevant laboratory experience.
- Experience with LC-MS instrumentation and software.
- Experience in a Good Laboratory Practices (GLP) and CRO environment.
- Ability to handle multiple projects, prioritize work, and meet deadlines.
Preferred Requirements
- Master’s degree or PhD in scientific related discipline.
- 3 to 5 years of experience in a Good Laboratory Practices (GLP) environment.
- Experience with Shimadzu and SCIEX instrumentation.
- Experience with Watson.
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
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