SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced ... self-injection devices. With a global team of 6,000 employees, we partner with leading ...
SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced ... self-injection devices. With a global team of 6,000 employees, we partner with leading ...
Software QA Engineer II
Newton, MA · On-site
$50 - $60/hr
... and dedicated medical devices to improve procedural outcomes and access to care. Key ... software QA/testing experience, particularly with application software and hardware systems.
New
Software QA Engineer II
Newton, MA · On-site
$50 - $60/hr
... and dedicated medical devices to improve procedural outcomes and access to care. Key ... software QA/testing experience, particularly with application software and hardware systems.
New
The Senior Software QA Engineer will be responsible for developing and executing advanced software ... Experience within medical technology, medical devices, diagnostics, or another regulated product ...
The Senior Software QA Engineer will be responsible for developing and executing advanced software ... Experience within medical technology, medical devices, diagnostics, or another regulated product ...
Senior Software QA Engineer
Norwood, MA · On-site
The Senior Software QA Engineer will be responsible for developing and executing advanced software ... Experience within medical technology, medical devices, diagnostics, or another regulated product ...
Senior Software QA Engineer
Norwood, MA · On-site
The Senior Software QA Engineer will be responsible for developing and executing advanced software ... Experience within medical technology, medical devices, diagnostics, or another regulated product ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
Understand concepts of Software and Firmware integration testing of medical devices that ensure ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...
What you will do as a Software Quality Assurance Engineer: * Embed with engineering teams to ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
Quick apply
What you will do as a Software Quality Assurance Engineer: * Embed with engineering teams to ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
To succeed as a Software Quality Assurance Engineer, you will need the followingexperience and ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
To succeed as a Software Quality Assurance Engineer, you will need the followingexperience and ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
To succeed as a Software Quality Assurance Engineer, you will need the followingexperience and ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
To succeed as a Software Quality Assurance Engineer, you will need the followingexperience and ... Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with ...
Design Software Quality Consultant (Medical Devices) Location: REMOTE Duration: Long Term Position Overview We are seeking an experienced Design Software Quality Consultant to support post ...
Quick apply
Design Software Quality Consultant (Medical Devices) Location: REMOTE Duration: Long Term Position Overview We are seeking an experienced Design Software Quality Consultant to support post ...
Sr. Software QA Engineer
Newton, MA · On-site
$58 - $60/hr
Experience in testing safety-critical software systems preferred (e.g., automotive, medical devices ... quality assurance, with a focus on application software and hardware systems. Familiar ...
New
Sr. Software QA Engineer
Newton, MA · On-site
$58 - $60/hr
Experience in testing safety-critical software systems preferred (e.g., automotive, medical devices ... quality assurance, with a focus on application software and hardware systems. Familiar ...
New
Senior Quality Assurance Engineer, Medical Devices
Charlottesville, VA · On-site
$75K - $105K/yr
Senior Quality Assurance Engineer - Medical Devices Charlottesville, VA 22911 * Department: Quality ... software tools, and process optimization projects * Provide technical quality guidance to cross ...
Quick apply
Senior Quality Assurance Engineer, Medical Devices
Charlottesville, VA · On-site
$75K - $105K/yr
Senior Quality Assurance Engineer - Medical Devices Charlottesville, VA 22911 * Department: Quality ... software tools, and process optimization projects * Provide technical quality guidance to cross ...
Software Quality Assurance
Houston, TX · On-site
Software Quality Assurance Engineer** who is fueled by high ownership, execution horsepower, growth ... medical conditions), sexual orientation, gender identity, gender expression, age, status as a ...
Software Quality Assurance
Houston, TX · On-site
Software Quality Assurance Engineer** who is fueled by high ownership, execution horsepower, growth ... medical conditions), sexual orientation, gender identity, gender expression, age, status as a ...
... Assurance activities in an FDA-regulated medical device environment and ensuring that software ... Experience in supporting the manufacturing of medical devices or other regulated industry.
... Assurance activities in an FDA-regulated medical device environment and ensuring that software ... Experience in supporting the manufacturing of medical devices or other regulated industry.
Bachelor's degree in Engineering, Life Sciences, or a related field, or an equivalent combination of education and experience. * 2-5 years of Quality Assurance experience in a medical device ...
Bachelor's degree in Engineering, Life Sciences, or a related field, or an equivalent combination of education and experience. * 2-5 years of Quality Assurance experience in a medical device ...
Bachelor's degree in Engineering, Life Sciences, or a related field, or an equivalent combination of education and experience. * 2-5 years of Quality Assurance experience in a medical device ...
Quick apply
Bachelor's degree in Engineering, Life Sciences, or a related field, or an equivalent combination of education and experience. * 2-5 years of Quality Assurance experience in a medical device ...
More experienced candidates are encouraged to apply for the SDET position. Futurex is seeking ... cryptographic devices and report conclusions in a clear and concise manner. * Develop new tests ...
More experienced candidates are encouraged to apply for the SDET position. Futurex is seeking ... cryptographic devices and report conclusions in a clear and concise manner. * Develop new tests ...
Software QA Engineer
San Jose, CA · On-site
They are seeking a Software QA Engineer to prepare devices for testing, execute test cases, log bugs, and collaborate with development teams to improve software validation coverage. Responsibilities ...
Software QA Engineer
San Jose, CA · On-site
They are seeking a Software QA Engineer to prepare devices for testing, execute test cases, log bugs, and collaborate with development teams to improve software validation coverage. Responsibilities ...
Software Quality Assurance
Raritan, NJ · On-site
Software Quality Assurance Location: Raritan, NJ (Hybrid) Duration: 6-12 Months+ Tax: W2 Only * Knowledge of CI/CD * Should know how to work in Agile, Jenkins, Puppet, Chef, Jira, Bitbucket, and ...
Software Quality Assurance
Raritan, NJ · On-site
Software Quality Assurance Location: Raritan, NJ (Hybrid) Duration: 6-12 Months+ Tax: W2 Only * Knowledge of CI/CD * Should know how to work in Agile, Jenkins, Puppet, Chef, Jira, Bitbucket, and ...
Software Quality Assurance Medical Devices information
See salary details
$15.14 - $19.62
5% of jobs
$19.62 - $24.10
1% of jobs
$24.10 - $28.58
4% of jobs
$28.58 - $33.06
8% of jobs
$36.28 is the 25th percentile. Wages below this are outliers.
$33.06 - $37.54
8% of jobs
$37.54 - $42.02
13% of jobs
The median wage is $45.06 / hr.
$42.02 - $46.50
15% of jobs
$46.50 - $50.98
16% of jobs
$52.71 is the 75th percentile. Wages above this are outliers.
$50.98 - $55.46
12% of jobs
$55.46 - $59.94
12% of jobs
$59.94 - $64.42
6% of jobs
$15
$44
$64
How much do software quality assurance medical devices jobs pay per hour?
What is the difference between Software Quality Assurance Medical Devices vs Software Validation Engineer?
| Aspect | Software Quality Assurance Medical Devices | Software Validation Engineer |
|---|---|---|
| Certifications | ISO 13485, IEC 62304, FDA regulations | ISO 13485, IEC 62304, FDA regulations |
| Work Environment | Medical device manufacturing, regulated labs | Product development, testing labs |
| Industry Usage | Medical device companies, healthcare | Medical device and software companies |
| Primary Focus | Ensuring quality and compliance of software in medical devices | Validating software functions and performance |
Both roles require similar certifications and work within regulated environments. Software Quality Assurance Medical Devices focuses on maintaining quality and compliance throughout the development process, while Software Validation Engineer emphasizes testing and verifying software functionality. Understanding these distinctions helps professionals choose the right career path or role in the medical device industry.
What are popular job titles related to Software Quality Assurance Medical Devices jobs?
For Software Quality Assurance Medical Devices jobs, the most frequently searched job titles are:

QA Specialist - GMP & Quality Assurance (Medical Devices)
Deerfield Beach, FL • On-site
Other
Posted 10 days ago
Key responsibilities
Review and approve Production Batch Records and Testing Results to ensure completeness, accuracy, and documentation compliance.
Provide oversight and support during manufacturing operations, including reviewing and approving Quality Work Instructions, Technical and Product Specifications, Sampling instructions, and Test Methods.
Support investigation processes for Non-Conformances and ensure completion of corrective and preventive actions.
Job description
SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.
Job Overview
QA Specialist provides oversight of GMP operations to ensure that products are manufactured according to cGMP requirements and fit for their intended use. Maintains data collected from the manufacturing process, generates, and updates procedures and ensures Batch Records comply with established policies and procedures.
Main Responsibilities
- Review and Approve Production Batch Records and Testing Results to ensure they are complete, accurate and documented according to established procedures.
- Prepare CofC and CoAs.
- Maintains QA manufacturing floor presence in support of manufacturing operations and provides oversight over process related decisions.
- Reviews and approves Quality Work Instructions (QWIs), Technical and Product Specifications, Sampling instructions and Test Methods.
- Provides oversight to Risk Management programs, procedures, and documentation for Development and Process Validation activities.
- Review and approve Test Method Development, Validation, and Transfer activities in support of the Analytical Sciences department.
- Review and approve Stability Studies protocols and reports.
- Support the investigation process for Non-Conformances and ensures completion of related corrective and preventive actions.
- Support the Audit Team with during external and internal audits.
- Provides support to the program management office with the review and approval of the design transfer package documentation.
- Provides Quality support for throughout the product lifecycle to include the review of Annual product reviews, Product Process Monitoring activities and Continuous Improvement initiatives.
- Preferred BS in Engineering, Biology, or other technical related degree
- A minimum of 4 years of experience in Quality with Pharmaceutical and/or Medical Device based GMP manufacturing operations.
- Proficient skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities.
- Demonstrate proficient ability to evaluate and apply compliance requirements/guidelines to complex situations.
- Knowledge of regulations and practices pertaining to pharmaceutical/medical device products in area of responsibility.
- Ability to interact with regulatory agencies. knowledge of FDA, EMA, JP and other regulations.
- Knowledge of Good Manufacturing Practices & Good Documentation Practices
- Able to communicate effectively and work within cross-functional teams.
- Excellent oral and written communication skills with strong technical writing experience required.
- Experience in internal / external audits, identify findings, drive resolution, and provide closure report
- Proficient skills in solving complex problems and ability to bring issues to resolution.
- Experience working globally with diverse teams and cultures
- Competitive compensation package
- Modern working environment with state-of-the-art facilities and technologies
- Challenging assignments in a fast growing and innovative industry
- Position in a dynamic, international team of highly skilled professionals
- Various opportunities for personal and professional development within a global organization
For more information on SHL Medical, please visit: shl-medical.com
About the company
SHL Medical
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#J-18808-LjbffrAbout SupportFinity
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Industry
It services and recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
San Francisco, CA, US