Quality Auditor

at  Charles River Laboratories

Req ID #: 224268
Ballina, Connacht, IE
Full time
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

JOB SUMMARY

We are seeking an experienced Quality Auditor (Fixed Term Contract x 12 Months for Maternity Leave cover) for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the QA Manager and the main duties & responsibilities shall be:

• Perform general auditing duties for compliance with quality standards.
• Prepare written reports on audit and inspection activities.
• Review SOPs.
• Assist in the administration of the Quality Department and of Quality systems.
• Assist with Vendor Assessment, client audits and subcontractor audits.

JOB QUALIFICATIONS

The following are minimum requirements related to the Quality Auditor position.

• BSc. in a Science discipline
• Established experience of working within a GLP/GMP environment is preferable, but not essential to the role
• Previous quality auditing experience preferable.
• Meticulous attention to detail and high level of accuracy.
• Comfortable working with calculations.
• Ability to work both individually and within a team
• Excellent interpersonal & communication skills both written and verbal.
• IT Skills – MS Word, Excel, PowerPoint.

• Perform general auditing duties for compliance with quality standards.
• Prepare written reports on audit and inspection activities.
• Review SOPs.
• Assist in the administration of the Quality Department and of Quality systems.
• Assist with Vendor Assessment, client audits and subcontractor audits