Performs assembly, diagnosis, test, and repair work per established work instructions, policies, and procedures.
Operating within standard operating procedures (SOPs) and assembly drawings.
Communicate with quality and facilities any time there is an issue with the product or equipment.
Provide guidance in problem diagnosis and resolution with team members.
Assist in development and revisions of Standard Operating Procedures (SOP), Work Instructions (WI) device history records, or other quality documentation, as necessary, to support production processes.
Comply with EHS and Quality procedures, regulations and policies.
Education / Experience / Skills :
Recent Bachelor’s degree in Biomedical / Bioengineering or related scientific field.
Experience working in cGMP setting and controlled documentation