Quality Intern

Working at Freudenberg: We will wow your world!

Responsibilities:

• Support the validation activities for a new machine on the manufacturing floor.

• Update procedures in our electronic document management system.

• Assist with the validation activities for a new labeling software program.

• Create new documentation and review existing documentation for compliance with regulations and procedures.

Qualifications:

• Bachelor's Degree (in progress or completed).

• High attention to detail.

• Goal oriented.

• Strong interpersonal, oral and written communication skills.

• Some prior experience with writing and executing Engineering reports and studies.

• Some prior experience with coding/programming.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical LLC