This is a paid internship (obviously) with the opportunity for a candidate to gain insight into a large part of our quality, regulatory, and manufacturing operations.
Please have the candidates forward their resume or call me directly.
Summer Internship – Medical Device Manufacturer
The summer internship shall be part of the Quality and Regulatory department of a local medical device manufacturer.
The position shall report directly to the Vice President, Global QA/RA & Technology.
The position includes exposure to the quality and regulatory operations of an FDA regulated medical device manufacturer, manufacturing operations, and product development.
The candidate shall become integrated in the department through documentation review, writing, updating, and posting procedures, work instructions, and product development related information.
Some interaction in the manufacturing environment shall be part of the overall process including quality inspections and assessments.
Minimum skill-set and requirements shall include:
-Understanding and use Microsoft Office (Word, Excel mainly)
-Ability to effectively write/update, screen, and understand documentation (preferably related to manufacturing procedures and work instructions)
-Basic understanding of manufacturing operations and production flow (not required, but desired)
-Detail oriented mindset for documentation review and updates
Contact:
Sincerely,
Paul Lloyd
Vice President, Global QA/RA & Technology
