Quality Manager
If you can drive quality improvements through the creation of new or enhancing processes, while positively influencing production employees; then you should be successful at Oakworks.
We are looking for a Quality Manager with experience in medical devices strongly preferred.
The Quality Manager takes a data driven approach to deliver quality initiatives and acts as a change agent in the organization, while managing (2) Quality Specialists.
The Quality Manager is responsible for the administration, oversight of quality control and release of finished product, supplier quality/ auditing, non-conforming material.
Applying risk management principles (ISO 14971), and an advocate of continuous improvement.
Additionally experience desired in design assurance for new product development including design transfer process.
Hours and Status:
The normal schedule is Monday through Friday with some flexibility on start and end times.
This is a full time, benefits eligible position.
Oakworks is a family owned and run company for over 40 years that produces world class medical, spa and massage 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, generous company bonus plan, paid time off, 9 paid holidays and opportunities for advancement.
Oakworks focuses on the quality of our products and 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.
Must have a BS degree in Engineering or related Bachelor's degree.
10 to 15 years' experience in a Quality Management role with medical device experience (Class 1 and 2) strongly preferred along with knowledge of FDA 21CFR 820, ISO 13485, ISO 9001, ISO 14971 and IEC 60601.
American Society for Quality (ASQ) QE, Internal auditor ISO 13485/ISO 9001 and Six sigma, lean manufacturing certification preferred.
The proven ability to drive quality improvement in a manufacturing environment with advanced computer skills, investigation and root cause analysis, trending analysis, project and Quality System software are required.
Physical requirements include the ability to sit/stand/walk for extended periods of time on a daily basis.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
We are looking for a Quality Manager with experience in medical devices strongly preferred.
The Quality Manager takes a data driven approach to deliver quality initiatives and acts as a change agent in the organization, while managing (2) Quality Specialists.
The Quality Manager is responsible for the administration, oversight of quality control and release of finished product, supplier quality/ auditing, non-conforming material.
Applying risk management principles (ISO 14971), and an advocate of continuous improvement.
Additionally experience desired in design assurance for new product development including design transfer process.
Hours and Status:
The normal schedule is Monday through Friday with some flexibility on start and end times.
This is a full time, benefits eligible position.
Oakworks is a family owned and run company for over 40 years that produces world class medical, spa and massage 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, generous company bonus plan, paid time off, 9 paid holidays and opportunities for advancement.
Oakworks focuses on the quality of our products and 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.
Must have a BS degree in Engineering or related Bachelor's degree.
10 to 15 years' experience in a Quality Management role with medical device experience (Class 1 and 2) strongly preferred along with knowledge of FDA 21CFR 820, ISO 13485, ISO 9001, ISO 14971 and IEC 60601.
American Society for Quality (ASQ) QE, Internal auditor ISO 13485/ISO 9001 and Six sigma, lean manufacturing certification preferred.
The proven ability to drive quality improvement in a manufacturing environment with advanced computer skills, investigation and root cause analysis, trending analysis, project and Quality System software are required.
Physical requirements include the ability to sit/stand/walk for extended periods of time on a daily basis.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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