[Hiring] Quality Assurance Regulatory Affairs Project Specialist @OAKWORKS INC
Role Description If you have a holistic team approach to improve quality, we want to develop you! Oakworks has an opportunity if you have regulatory and quality assurance experience in a medical device environment. This role is analytical and hands-on and is responsible for our regulatory requirements and document control processes.
Qualifications
- Must have Bachelor’s Degree or equivalent ideally in sciences, engineering, or another relevant scientific discipline.
- 5 years of professional experience in QARA; quality management systems relating to medical devices (FDA 21CFR 820, ISO 13485, ISO 14971).
- Advanced computer skills, trending analysis, project and Quality System software experience (QT9 preferred) are required.
Requirements
- None specified.
Benefits
- A platform in providing health and wellness solutions.
- Friendly, fun, clean and a safe work environment.
- Competitive wage and benefits.
- Ability for growth.
- Being a member of an innovative company.
Company Description
Oakworks is a family owned and run company for over 40 years that produces world class medical and spa equipment in our modern 91,000 sq ft building. You will be helping to build a wide array of products with a great team of people.
- We offer a 401k plan, paid time off, 9 paid holidays and opportunities for advancement.
- Oakworks does not only focus on the quality of our products but also cares about our employees.
- Oakworks is proudly promoting health awareness through different activities within the company.
- We strive on being an employee centered workplace and hold multiple fun events to show our appreciation.
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