Provide support for Surgical development projects from project inception through successful Technology Transfer/Scale-Up at the manufacturing facility. Additionally the role will support marketed product changes and updates (MOB). The role includes working with multidisciplinary teams to insure medical device development activities are planned and executed in compliance with Design Control Requirements and Bausch + Lomb/Valeant procedures. Provide Quality Assurance support to sites as needed.
Location to be either in Rochester NY or Clearwater FL
Represent Design Quality on multi-disciplinary new product development and MOB teams. Duties will include:
Currently there are no direct or indirect reports associated with this position.
Bachelor’s Degree (BS) in engineering or scientific discipline (Chemistry, Biology, Microbiology).
Five years experience in Medical Device and/or Pharmaceutical Industry in Quality, R&D, Engineering or Laboratory environment. Specific experience desired is as follows: