ISO 13485 Lead Auditor

RQM+ is the largest global MedTech CRO, offering consulting, clinical trial, lab and reimbursement services across the entire product lifecycle. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to promote economic growth through regional partnerships, provide a rewarding place to work, and improve our communities.

ISO 13485 Lead Auditor

To help support our ever growing and expanding Global Audit Practice, we’re interested in speaking to Auditors who would be interested in supporting RQM on various supplier/vendor audits on a contract basis for our clients in Europe. These will be a mixture of on-site and remote desktop audits.

We’re interested in speaking to ISO 13485 Lead Auditors with a background in any of the following fields:

• ISO 13485:2016
• EU MDR
• ISO 17025:2017 for Calibration and Laboratory
• ISO 27001:2022
• PCBA (printed circuit boards)
• Machining/casting
• Injection moulding
• Mechanical hardware
• Repair activity

Being an industry leader in regulatory and quality consulting is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!

We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.