Job Summary: We are seeking a Quality Engineer with knowledge of Medical Device Manufacturing and a compliance background. This role demands a solid understanding of quality system requirements for medical device companies. The primary responsibility will be to execute Corrective and Preventive Actions (CAPA) and provide support to the existing Quality Engineering team.
Key Responsibilities:
- Execute CAPA processes, managing approximately 30-40 open CAPAs.
- Provide relief to the existing Quality Engineering team, allowing them to focus on production and sustaining activities.
- Process non-conforming products and execute identified corrective actions.
- Update procedures and support production activities.
- Work collaboratively in a team setting.
Required Skills and Qualifications:
- Knowledge of Medical Device Manufacturing and compliance requirements.
- Ability to prioritize tasks and execute projects/actions with minimal guidance.
- Proficiency in Microsoft Office Suite.
- Experience with quality system requirements for medical device companies.
- Strong problem-solving skills and attention to detail.
- Ability to work independently and as part of a team.
Preferred Qualifications:
- Quality Engineers with an understanding of the medical device field.
- Previous experience in a similar role is a plus.
Contract Details:
- 3 month contract, with the possibility of extension
If you are a motivated individual with a background in medical device manufacturing and compliance, and you are looking for a short-term opportunity to make a significant impact, we encourage you to apply.
