In this position, you will be working closely with various departments across the business to pursue quality related matters for the medical product portfolio. You will need to encourage,promote and maintain GMP across the business and be a point of support for all quality related issues. You will be responsible for the product compliance audit schedule and will need to conduct internal, external and third-party audits. You will also need to ensure compliance with ISO 13485 & maintain the CAPA process.
Key experience/skills required are...
- Experience of working with ISO 13485:2016
- Previous experience of working in a manufacturing environment
- An internal auditor certificate for ISO 13485 is preferred
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.