In this role there are opportunities to support the business in both QA, RA & validation and training can be offered on all three if required. Some of the responsibilities involve CAPA investigations, the review of non-conformities & finished product batch release. The QMS ISO 13485 will need to be developed and maintained and as a team, this will be one of the main focuses.
Required experience includes...
- Previous experience in a medical manufacturing environment (No time frame required)
- Working knowledge of ISO 13485
- Previous experience in working in either QA, RA or validation.
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.