Staff Scientist I - TLM

QPS’ Translational Medicine (TLM) Department seeks a Staff Scientist I!

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!

As a Staff Scientist I in TLM, you will be a key contributor in a laboratory role focused on the analysis of drug or other targets in complex biologic matrices using immunologic methods. Responsibilities will include laboratory stewardship, wet-lab operations as well as data reduction and documentation.

QPS’ Story

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.

If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com [http://www.qps.com]) for more information and to see all current openings.

Please note - this role is not eligible for visa sponsorship now or in the future. Applicants should already have permanent or fully unrestricted authorization to work in the United States

• The Job
• Set-up, use and maintain complex, state of the art, instrumentation
• Proficiently execute complete assays, daily and independently, in accordance with the GLPs and governing policies and SOPs to avoid failed runs and study findings
• Document results, accurately record observations, and maintain study records in accordance with the GLPs and governing policies and SOPs to avoid failed runs and study findings
• Prepare report documents and author final sample analysis (SA) reports
• Prepare data tables and/or write reports

• Work Location