Scientist II LCMS

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. Responsibilities: Prepare reagents, standards, and control samples Analyze samples using various techniques specific to department Perform complex method development with limited supervision Perform method validation or qualification Operate analytical equipment Lead 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 Record tasks in accordance with Good Documentation Practices (GDP) Understand and apply 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 7-8 years lab experience; all experiences will be evaluated PhD in relevant field Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP Able to independently 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 and knowledge of & experience in regulatory environment Competencies: Adaptable Exactness Flexibility Collaborative Effective Listener and Communicator Capacity to Master and Influence Others Results Driven Creative and Forward Thinking Initiative Supportive Extend Assistance Strategic Minded Physical Demands: Must be able to sit at a desk for up to 6 hours per day Walking and/or standing as required for the rest of the working day Must be able to occasionally lift 15 lbs.; this includes lifting boxes, equipment, etc. Bending or standing as necessary The length of time of these tasks may vary from day to day and task to task