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Job Requirements of Senior Software Quality Assurance Engineer - Canton, MA:
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Employment Type:
Full-Time
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Location:
Canton, MA (Onsite)
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Senior Software Quality Assurance Engineer - Canton, MA
This position is for a talented Senior Software Quality Assurance Engineer / Software QA Engineer to join an industry leading medical device organization just south of Boston to work on some revolutionary medical devices, and lead the development, review, and execution of software quality assurance processes and procedures for assigned projects within the organization.
Client Details
This organization is an industry leading medical device company that are a global provider of scientific and analytical solutions. They have locations in both the US and the UK!
Description
Some of the responsibilities for the successful Senior Software Quality Assurance Engineer / Software QA Engineer will include:
- Lead the development, review, and execution of software quality assurance processes and procedures for projects within the organization
- Collaborate with teams in all areas of the organization to ensure software development and validation activities meet quality and compliance requirements
- Perform risk assessments and develop mitigation strategies for software-related issues
- Conduct software validation activities in accordance with regulatory standards (FDA, ISO 13485)
- Review and approve software documentation, including validation plans, protocols, and reports
Profile
The suitable Senior Software Quality Assurance Engineer / Software QA Engineer will have the following experience:
- 3+ years experience as a Software Test / Software Quality Assurance Engineer
- Demonstrated commercial ownership in writing validation plans for a new product
- Experience writing the test suite for new product development in a regulated industry (medical device preferred but other regulated industries are also acceptable)
- A knowledge of requirements and how to work off requirements and successfully test a device
- Cyber Security experience through a recent FDA submission
- ISO 13485 experience
- CFR compliance experience
- Objective Performance Criteria (OPC) experience
- Great communication - both written and verbal
Job Offer
- Excellent benefits (Medical, Dental, Vision, 401k)
- Annual bonus on offer
- Flexibility to work hybrid when possible
- Generous PTO
- Excellent growth potential
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.