LC-MS/MS Scientist/Bioanalytical Principal Investigator

122 Altasciences Preclinical Columbia LLC; State Road (DE); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Health Insurance

401(k) Match

Paid Vacation

Sick Leave

Telehealth

Training Program

Referral Bonus

Performance Review

Job summary

Altasciences seeks a Scientist/Bioanalytical Principal Investigator to lead LC-MS/MS analyses for regulated nonclinical studies, ensuring GLP compliance and timely reporting. The role involves client interaction, report writing, and collaboration with regulatory teams in a fast-paced CRO environment.

Ideal candidates have 5+ years in bioanalytical CRO settings with LC-MS expertise, and a strong GLP background. Master’s/PhD preferred for advanced projects and leadership duties.

Qualifications

• Minimum 5 years experience as a bioanalytical scientist in a CRO performing or overseeing regulated studies.
• Experience with LC-MS instrumentation and software.
• Experience in a Good Laboratory Practices (GLP) and CRO environment.

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.

Skills

Multi-project management

GLP compliance

Education

Bachelor's degree in Chemistry/Immunology/Biology

Master's degree or PhD in scientific related discipline

Tools

Shimadzu instrumentation

SCIEX instrumentation

Watson

Job description

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

• 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.

What You’ll Need to Succeed

• 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

Preferred Requirements

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

Work Authorization & Sponsorship

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

What We Offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

• Health/Dental/Vision Insurance Plans
• 401(k)/RRSP with Employer Match
• Paid Vacation and Holidays
• Paid Sick and Bereavement Leave
• Employee Assistance & Telehealth Programs

• Training & Development Programs
• Employee Referral Bonus Program
• Annual Performance Review

Company Culture & Diversity

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!

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