About The Role
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. 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
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.
Minimum 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) and CRO environment
Experience with LC-MS instrumentation and software
Ability to handle multiple projects, prioritize work, and meet deadlines.
Preferred Requirements
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
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
The pay range estimated for this position is $80,000 - $105,000 annually. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
Benefits
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth Programs
Altasciences' Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program
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Skills Required
- Bachelor's degree in Immunology, Biology, Chemistry, or another related scientific discipline
- At least 5 years of relevant laboratory experience
- Experience in a Good Laboratory Practices (GLP) environment
- Experience in a contract research organization (CRO) environment
- Experience with LC-MS instrumentation and software
- Ability to manage multiple projects, prioritize work, and meet deadlines
- Master's degree or PhD in a related scientific discipline
- 5 to 10 years of experience in a GLP environment
- Experience with Shimadzu and SCIEX instrumentation
- Experience with Watson software
What We Do
Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!
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