Review and maintain product compliance specifications, documentation control.
Gain proficiency in all testing areas.
Documentation of testing results and determination of aesthetic quality on the finished product.
Maintain consistency for training tasks in Master Control.
Maintain SOP criteria for inspection/testing.
Responsible for maintaining department equipment and ordering consumable stock supplies when necessary.
Exercise GMP and GLP compliance in the work environment.
Work well in a high-volume fast-paced environment.
Work closely with the Quality Assurance department as a quality team.
Work with the continuous improvement program within the department.
Understand and exercise all safety requirements and procedures.
Education + Experience
Possess a high school diploma or equivalent.
Some laboratory experience in a biological sciences laboratory is preferred.
A minimum combined 1-2 years of experience in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.
Some familiarity with FDA regulations for medical devices.
Possess the ability to manage many tasks and in an organized fashion.
Listen to, and follow, written and verbal instructions in English.
Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
Must be available to work alternate shifts when needed.