Will you share our mission to fight cancer? Dako, An Agilent Technologies Company is a world leading companies in tissue-based cancer diagnostics with a heritage of quality and innovation in antibodies and reagents. Our solutions are helping to unite the pathology lab and eliminate errors. We continuously challenge and raise the global standards for fast and accurate answers for cancer patients and doctors who make vital decisions for treatment. If you'd like to make a real difference to cancer diagnostics and advancing personalized medicine, join us.
This is an Intermediate position in Quality Control Department which will be responsible for performing real time stability studies for new products and stability monitoring for current products. Duties also include other Quality Control testing, production support and Device History Record review. This position requires the ability to write stability study protocols, implement studies and write reports within the project timeline.
Candidates should be well organized and detail oriented, possess a Bachelors Degree in a biological field and a minimum of 2 years experience in a Clinical or Quality Control laboratory. GMP/QSR/ISO background/ASCP certified Histotechnician or Clinical Laboratory Scientist is desired. Experience with Immunohistochemistry, InSitu Hybridization or Special Stains is preferred.
Agilent is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to disability, protected veteran status or any other protected categories under all applicable laws.