Bioanalytical Principal Investigator

CareAbout•Columbia, MO

2d•Onsite

About The Position

As Scientist/Bioanalytical Principal Investigator in the LC-MS/MS group at Altasciences, you will be responsible for the conduct of method validation and sample analysis related to assigned nonclinical bioanalytical studies utilizing LC-MS/MS instrumentation. 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.

Requirements

Associates/Bachelor’s degree in Chemistry/Immunology/Biology or equivalent in discipline
Minimum of 5 years experience as a bioanalytical scientist in a CRO performing or overseeing regulated studies
Minimum 5 years 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.
Applicants must be legally authorized to work in the United States.
All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

Nice To Haves

Master’s degree or PhD in scientific related discipline.
Experience with Shimadzu and SCIEX instrumentation.
Experience with Watson.

Responsibilities

Serve as Principal Investigator and contributing scientist for LC-MS/MS analysis in support of regulated nonclinical 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.
Plan, oversee and guide the timely completion of laboratory work in support of Method Validation and Sample Analysis for nonclinical studies using LC‑MS/MS
Maintain all documentation in support of Method Validation and Sample Analysis for assigned studies.
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 regulatory, FDA, GLP, ALCOA++, USDA, and AAALAC guidelines, in the conduct of assigned studies.
Use your knowledge and experience to mentor, train, and develop more junior team members.
Use your experience to improve and enhance processes and laboratory efficiency.