RA/QA Associate

RA/QA Associate

Location: Medical Device company in Netanya

Job Description:

Come join our vibrant, warm company as part of our RA/QA Department!

Our company is ISO 13485 certified, and constantly performs regulatory processes in various territories around the world. As an RA/QA associate, you will take part in the day-to-day quality processes, as well as creating technical files for various regulatory entities. You will also take part in the quality and regulatory aspects of the development of new products.

Responsibilities:

*Medical Device Regulation processes and certifications in various territories.

*Cosmetic Regulation processes and certifications in various territories.

*Partaking in the management of clinical/cosmetic trials and studies.

*Responsibility for various continuous quality tasks including – handling complaints, nonconformities, CAPAs and reworks.

*Partaking in annual quality tasks such as PMS, Risk Management and Audits (internal and external).

What are we looking for?

*A responsible and fast-learning people-person

*BA/BSc (must), preferably in a scientific field

*MA/MSc – an advantage

*Experience in quality/regulation – an advantage (on-the-job training)

*High-level of English (reading, writing and speaking) – a must