Exciting opportunity to work for a growing, dynamic Clinical Research Organization (CRO).
Resolian is looking for an experienced LC-MS Scientist with solid industry experience to join our team.
Responsibilites: • Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Independently design and develop methods • Perform method validation or qualification • Operate analytical equipment • Technical resource for troubleshooting activities; assays and equipment • Maintain analytical equipment • Review, evaluate, and interpret data results • Draft and present posters/presentations • Train and mentor lower level Scientists • Collaborate with clients and vendors • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Collaborate across teams, departments, and sites • Evaluate and establish processes to improve quality and efficiency • Record tasks in accordance with Good Documentation Practices (GDP) • Knowledge of regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Other tasks as assigned
Education, Experience & Skills Required:
BA/BS or higher with 11-12 years lab experience; all experiences will be evaluated
PhD in relevant field with 3-5 years lab experience
Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP
Able to independently develop and perform complex lab work
Able to work in a regulated environment
Able to work effectively and contribute within a team