Senior Quality Engineer - Medical Devices (3831-W)
Stout Systems
Elkton, MD
- Expired: November 03, 2022. Applications are no longer accepted.
We are searching for a Senior Quality Engineer with experience in ISO 13485 and ISO 14971 regulated device manufacturing.
LOCATION
Elkton, MD
This role will be performed 80% on site and 20% work from home.
COMPENSATION
$92K - $107K depending on skills and experience.
Excellent benefits including an annual 10% performance bonus and 6% 401K match.
EDUCATION
Minimum Bachelor's Degree in a relevant discipline such as Mechanical Engineering or Biomedical Engineering
REQUIRED FOR SENIOR QUALITY ENGINEER
ABOUT THIS ROLE
TAGS
Quality Engineer Regulated Environment Medical Device Process Engineer PFMEA DFMEA ISO 13485 ISO 14971 3831-W
Please submit resume and cover letter to recruit@stoutsystems.com with the job title/number in the email.
We have a bunch of technology jobs available! View more jobs at https://www.stoutsystems.com/jobs
We host free career webinars every week at https://www.stoutsystems.com/events
Requirements
EDUCATION
Minimum Bachelor's Degree in a relevant discipline such as Mechanical Engineering or Biomedical Engineering
REQUIRED FOR SENIOR QUALITY ENGINEER
Benefits
This role will be performed 80% on site and 20% work from home.
COMPENSATION
$92K - $107K depending on skills and experience.
Excellent benefits including an annual 10% performance bonus and 6% 401K match.
LOCATION
Elkton, MD
This role will be performed 80% on site and 20% work from home.
COMPENSATION
$92K - $107K depending on skills and experience.
Excellent benefits including an annual 10% performance bonus and 6% 401K match.
EDUCATION
Minimum Bachelor's Degree in a relevant discipline such as Mechanical Engineering or Biomedical Engineering
REQUIRED FOR SENIOR QUALITY ENGINEER
- Several years working as a Quality Engineer or Process Engineer for a medical device manufacturer.
- Solid experience in a role that is responsible for document reviews, compliance reviews and risk management.
- Solid experience with ISO 13485 and ISO 14971.
- Extensive experience with Corrective Action Preventive Action (CAPA) systems.
- Experience supporting an internal audit.
ABOUT THIS ROLE
- From time to time, this role may be involved in hands-on complaint investigations, however it will primarily focus on documentation review, compliance review, CAPA and risk management.
- The role will provide post-market reviews, analysis and reports.
- The role will support internal audits.
- This role is more focused on quality systems and less on the investigations themselves.
TAGS
Quality Engineer Regulated Environment Medical Device Process Engineer PFMEA DFMEA ISO 13485 ISO 14971 3831-W
Please submit resume and cover letter to recruit@stoutsystems.com with the job title/number in the email.
We have a bunch of technology jobs available! View more jobs at https://www.stoutsystems.com/jobs
We host free career webinars every week at https://www.stoutsystems.com/events
Requirements
EDUCATION
Minimum Bachelor's Degree in a relevant discipline such as Mechanical Engineering or Biomedical Engineering
REQUIRED FOR SENIOR QUALITY ENGINEER
- Several years working as a Quality Engineer or Process Engineer for a medical device manufacturer.
- Solid experience in a role that is responsible for document reviews, compliance reviews and risk management.
- Solid experience with ISO 13485 and ISO 14971.
- Extensive experience with Corrective Action Preventive Action (CAPA) systems.
- Experience supporting an internal audit.
Benefits
This role will be performed 80% on site and 20% work from home.
COMPENSATION
$92K - $107K depending on skills and experience.
Excellent benefits including an annual 10% performance bonus and 6% 401K match.
Stout Systems
Address
Elkton, MD
21921
USA
Industry
Manufacturing
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