Location: Pittsburgh, PA, 15219
Reports to: Quality Control Supervisor
Manages Others: No
Job Type: Biotechnology, Information Technology/Computer Systems
Education/Year’s Experience: Bachelor’s degree in a biological science with 3+ years experience or Master’s degree in a biological science with 1+ years experience. Should be in a GMP QC environment
Related Degree Programs: Chemistry, Biochemistry, Biology, Microbiology
A combination of experience and/or education will be taken into consideration.
Noveome Biotherapeutics, Inc. is a dynamic Biopharmaceutical company with innovative platform technology that represents a paradigm shift in the development of novel therapeutics. Unlike most drugs that are single molecules, Noveome’s product is a complex mixture of biological factors that is believed to have the ability to address a wide range of conditions and injuries. Noveome collaborates with major research centers to advance these therapeutic applications and has initiated clinical trials.
The Quality Control Analyst II is responsible for conducting routine chemical and biological testing of raw materials, intermediates, finished products, and stability samples. This position works independently while following defined standard operating procedures. This position also documents the testing process, performs an initial review of testing results and identifies trends. The Quality Control Analyst II will maintain data integrity and ensure compliance with laboratory safety procedures.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Please note, as a company rooted in innovative our positions are consistently evolving and we champion the development of all roles. This job description is not designed to contain comprehensive listing of all responsibilities that are required, as they may change to meet the ongoing needs of the Company.
Reliability Time Management Detail Oriented
Goal Oriented Continuous Learning Integrity
Work Environment/Physical Demands
Requires a combination of sedentary work and standing for extended periods of time in the Quality Control labs where personal protective equipment is required. Duties require fine finger dexterity, writing, typing, hearing, reading, and depth perception.
This is an hourly full time position with a regular schedule of Monday through Friday work hours. Extended hours may be needed on occasion to complete company objectives.
What Noveome Will do for You
Noveome provides transparency in expectations, encourages innovative thinking, opportunities for expanded learning, competitive salaries, and a clean safe work environment. Eligible employees will appreciate the comprehensive benefits package and wellness perks. Best of all you will enjoy working with colleagues at all levels in our open receptive work environment.
For consideration, please send your CV and cover letter to firstname.lastname@example.org.
Noveome Biotherapeutics, Inc. is committed to a policy of equal opportunity for all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, marital status, citizenship status, sexual orientation, disability, genetic predisposition or carrier status, military or veteran status, or any other protected characteristic in accordance with applicable federal, state, and local law.