Job Description

Responsibilities:

• 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 Bachelors degree in Biomedical/Bioengineering or related scientific field.
• Experience working in cGMP setting and controlled documentation
• SAP skills and experience.
• Six Sigma belt or LEAN ideology.

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