Quality Assurance Specialist
A leading family-owned company with ambitious growth plans in the pharmaceutical and medical device sectors seeks a Quality Assurance Specialist to join their team. This role involves ensuring the quality of development projects, including supplier qualification and risk management.
Responsibilities:
* Lead design and development activities to meet regulatory requirements.
* Perform supplier qualification processes, ensuring compliance with internal quality standards and regulatory requirements.
* Plan, conduct, and document supplier audits to assess adherence to ISO 13485 and MDR.
Requirements:
* A Master's degree in Engineering, Life Sciences, Pharmacy, or a related field.
* A minimum of 5 years of experience in a Quality Engineering or Supplier Quality role within the medical device industry (pharmaceutical experience is an asset).
* Strong knowledge of ISO 13485, MDR, and ISO 14971.
About the Company:
This global life science recruitment firm specializes in partnering with start-ups and fast-growing biotech and pharmaceutical organizations. The company provides a unique blend of search firm expertise and contingent service.
Why Work with Us:
We offer a dynamic work environment, unparalleled networking opportunities, and a quality-based approach to finding the best talent for your organization.