Global Quality Internal Auditor – Audits & Compliance

Getinge; Nashua (NH); On-site; USD 85,000 - 100,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with company match

Paid time off

Life Insurance

Disability benefits

Flexible Spending Accounts

Parental leave

Tuition reimbursement

Job summary

Getinge is seeking a Corporate Quality Internal Auditor to perform Global Internal Audits, ensuring compliance across sites and early warning of regulatory issues. The role requires leading audits, coordinating teams, and maintaining thorough documentation while travel is expected for about 35% of the time.

The position demands a BA/BS in a life science or related field with at least three years of quality audit experience and strong knowledge of medical device regulations (QSmR, ISO 13485:2016,

Qualifications

• Bachelor's Degree in life science or related discipline.
• Minimum 3 years' experience in Quality System Audit.
• Experience completing and maintaining audit documentation.
• Knowledge of US and worldwide medical device regulations; includes ISO 13485 and MDR.

Responsibilities

• Conduct Global Internal Audits to improve compliance.
• Coordinate and manage audits as lead auditor at various locations.
• Maintain documentation for internal audits in databases.
• Follow up on nonconformances and track audit trends.
• Prepare and present audit results and corrective actions.

Skills

Quality System Audits

Audit Documentation

Regulatory Knowledge

Travel Willingness

Education

Bachelor's Degree in Life Science

Job description

Getinge is seeking a Corporate Quality Internal Auditor to perform Global Internal Audits, ensuring compliance across sites and early warning of regulatory issues. The role requires leading audits, coordinating teams, and maintaining thorough documentation while travel is expected for about 35% of the time.

The position demands a BA/BS in a life science or related field with at least three years of quality audit experience and strong knowledge of medical device regulations (QSmR, ISO 13485:2016,