Lead LC-MS/MS Scientist – GLP Method Development

122 Altasciences Preclinical Columbia LLC; Columbia Township (MO); Hybrid; USD 110,000 - 140,000; Full time

Benefits offered by this job

Health insurance

401(k) employer match

Paid vacation and holidays

Paid sick leave

Telehealth programs

Training and development programs

Employee referral bonus

Job summary

Altasciences Preclinical Columbia LLC is seeking scientists to join the frontlines of discovery and preclinical evaluation. You will lead LC-MS/MS method development, validate analytical assays, and ensure GLP-compliant study execution with meticulous documentation.

Responsibilities include coordinating with clients, mentoring staff, and driving timely delivery of high-quality data. A science background with leadership potential is required.

Qualifications

• Advanced degree in chemistry, biology or pharmaceutical science with hands-on experience.
• Supervisory experience is a plus; leadership potential welcomed.
• Proficiency with laboratory information management systems and electronic notebooks.
• Excellent communication of complex scientific concepts to clients and colleagues.
• Authorized to work in the United States without sponsorship now or in the future.

Responsibilities

• Lead development and validation of LC-MS/MS assays for preclinical and clinical study support.
• Perform study sample analysis focusing on toxicological and biological endpoints.
• Ensure GLP compliance and meticulous documentation throughout study work.
• Manage project timelines and coordinate with clients on study design and results.
• Mentor laboratory staff and provide scientific guidance to the team.
• Contribute to method validation and qualification efforts.

Skills

Supervisory skills

Communication skills

Technological savvy

Work authorization (US)

Education

Bachelor/Master/PhD in chemistry or biology or pharmaceutical science

Tools

LIMS

Electronic notebooks

Job description

Altasciences Preclinical Columbia LLC is seeking scientists to join the frontlines of discovery and preclinical evaluation. You will lead LC-MS/MS method development, validate analytical assays, and ensure GLP-compliant study execution with meticulous documentation.

Responsibilities include coordinating with clients, mentoring staff, and driving timely delivery of high-quality data. A science background with leadership potential is required.