Quality Engineer - (Toms River, NJ)

Two Quality Engineers Needed. 3-5yrs of Engineering background in Pharmaceutical, Biomedical or Medical Device companies is needed. Knowledge of Regulatory Guidelines and background writing validation protocols required. Overview of Quality Engineer responsibilities: This position is responsible for duties associated with cleaning validation processes and monitoring of cleaning verification activities consistent with cGMP qualifications for clinical manufacturing, scale-up and commercial manufacture of sterile and specialty pharmaceutical products. Major job functions include: generation of qualification / validation documents, execution of qualification / validation documents, generation of reports, managing resources, managing project time lines, interacting with clients, and participating in cross functional teams. Position overview for Quality Engineer: