Senior Scientist I LCMS

Resolian • Malvern, AR

37d

About The Position

Resolian is a Contract Research Organization (CRO) specializing in Drug Metabolism and Pharmacokinetic (DMPK) and bioanalytical services for both small and large molecules. At Resolian, we work to bring together and develop exceptional employees and colleagues who share our passion for generating significant contributions to the world. We take pride in our work and our employees. Resolian strives to help you and your family by offering a comprehensive benefits package. Our total rewards are designed to recognize outstanding performance and meet the diversified needs of all our colleagues – at every stage of their professional and personal lives. We continually strive to maintain the highest standards of professional ethics, scientific excellence, and regulatory compliance. We work to build trusted partnerships with each of our employees. Please consider joining our experienced & knowledgeable staff. Resolian is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status age or disability status.

Requirements

• 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
• Able to work with computer systems
• Able to document clearly
• Able to communicate clearly

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 251-500 employees