DescriptionAzzur Group is seeking an accomplished Equipment Validation Engineer to work with a Medical Device client in the Los Angeles area.
Responsibilities and Duties: Equipment and tooling qualifications/validations.
Protocol/report writing and execution.
Tooling design and FAI.
Writing procedures and creating production routers Test method development and validation; gage R Experience with statistics; Minitab is a plus Experience with CAD; Solidworks is a plus Other tasks may be assigned to satisfy project requirements with pre-approval of Azzur team management.Requirement BS in Engineering, Science or equivalent technical 3-10 years of engineering or related experience in a regulated, manufacturing environment within the medical device industry Excellent written and verbal communication skills; excellent technical writing Ability to work effectively in a fast-paced multitasking environment.
Strong working knowledge of FDA and cGMP regulations and documentation Proficient in Microsoft Word, Excel, PowerPoint.