Scientist II (LC-MS)

CareAbout•Everett, WA

11d•$80,000 - $105,000

About The Position

As an LC-MS scientist, 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.

Requirements

Bachelor’s degree in Immunology/Biology/Chemistry or other scientific related discipline plus a minimum of 5 years of relevant laboratory experience
Experience in a Good Laboratory Practices (GLP) environment
Experience with LC-MS instrumentation and software
Ability to handle multiple projects, prioritize work, and meet deadlines.

Nice To Haves

Master’s degree or PhD in scientific related discipline
5 to 10 years of experience in a Good Laboratory Practices (GLP) environment
Experience with Shimadzu and SCIEX instrumentation
Experience with Watson

Responsibilities

Maintain open and direct communication and attend recurring calls with clients.
Serve as principal investigator or contributing scientist for LC-MS studies.
Prepare all necessary driving documents for in-lab analysis.
Complete and deliver scientific reports to clients on time.
Prepare materials, including animal blood and tissues, for analytical assays to be run on LC-MS instrumentation.
Maintain and document chain of custody for specimens, reagents, controls, and samples in the laboratory.
Perform the assays according to protocol or other guiding documents with accurate documentation.
Maintain and update facility records related to the laboratory and its analyses.
Review laboratory records, procedures, and study data for completeness and accuracy.
Assist in calibration, optimization, maintenance, and collection of data from analytical instruments.
Perform routine laboratory maintenance (including cleaning, stocking supplies, equipment maintenance tasks, etc.).
Document deviations to laboratory procedures and study protocols in a timely manner and provide input for corrective actions.
Collaborate with internal regulatory departments to ensure quality and compliance oversight on GLP studies.
Follow Altasciences' Standard Operating Procedures (SOPs), ensure compliance with GLP, FDA's ICH M10 guidelines, ALCOA+, USDA, and AAALAC guidelines, and can identify areas for improvement.