Overview
Talent Title: Quality engineer
Location: Plymouth, MN
Duration: 24 Months
Description: Quality engineer experienced with internal or external auditing to internal QMS requirements; understands 21 CFR 820, ISO 13485, and CGMP Regulations.
Responsibilities
- Understand QMS requirements at a detail level
- Review product and QMS documentation to evaluate compliance
- Maintain an internal audit schedule
- Assist in communicating internal audit agendas and scheduling
- Participate in internal audits
- Generate Internal Audit reports
- Review and approve product and QMS work products as required
- General Quality Engineer tasks as required
Qualifications
- Experience with internal or external auditing to QMS requirements
- Knowledge of 21 CFR 820, ISO 13485, and CGMP Regulations
Seniority level
Mid-Senior level
Employment type
Contract
Job function
- Quality Assurance
Industries
- Medical Equipment Manufacturing
- Pharmaceutical Manufacturing