What are the responsibilities and job description for the Staff Scientist I position at QPS?
QPS’ Translational Medicine (TLM) Department is continuing to grow…you should be a part of that growth!
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.
This position is just the tip of the growth iceberg. Please visit our careers page to see other positions ranging from entry-level analyst to Research Scientist and Team Lead.
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, team work 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 () for more information and to see all current openings.
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
Requirements
The successful candidate will hold a degree in Biochemistry, Immunology, Pharmacology, Medical Technology, Biology or a related field as follows :
Why You Should Apply
QPS, LLC is an Equal Employment Opportunity / Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
