LC-MS/MS Scientist/Bioanalytical Principal Investigator

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.  No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About The Role
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.

What You'll Do Here

• 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.

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!