Scientist- LCMS

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.

• 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.).

• 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.

• 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.