Associate Scientist I
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 5-6 years lab experience; all experiences will be evaluated
- Able to 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; knowledge of and experience in a regulatory environment
Responsibilities
- Prepare reagents, standards, and control samples
- Analyze samples using various techniques specific to department
- Assist with method development
- Perform method validation or qualification
- Operate analytical equipment
- Lead troubleshooting activities
- Maintain analytical equipment
- 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
- Review and evaluate data results
- Train lower level Scientists
- Other tasks as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Industry
Professional, Scientific, and Technical Services
