What are the responsibilities and job description for the Embedded Firmware Test Engineer position at Medical Engineering Consultants (MEC)?
Job 2790 - Embedded Firmware Test Engineer - Contract located in Los Angeles County, California
Medical Engineering Consultants (MEC) support medical device and pharmaceutical companies to be more efficient and productive by providing resources, knowledge, and expertise to augment and supplement to their work. Our vision is to closely align our clients’ needs with the best resources available in the marketplace. We take proactive, preventative, and corrective action and create a roadmap for ongoing future improvement by identifying, integrating, and executing sustainable solutions that validate processes, ensure fully compliant quality systems, and close gaps between current and FDA expected stages.
MEC offers companies short or long-term support — from high-end leaders, managers and consultants to skill-set Engineering staff and SME’s (Subject Matter Experts).
MEC's mission is to inspire positive cultural change from within, and always exceed our clients’ expectations.
Applicants must be authorized to work in the U.S. in accordance with applicable law. This position is not eligible for employer-sponsored work authorization now or in the future.
Hybrid
Job Purpose
Develops embedded software firmware unit / integration tests firmware requirements and firmware verification tests.
Responsible for analyzing designing programming debugging and modification of an embedded software code base of a class III medical device.
May interface with cross-functional teams to define system requirements and/or necessary modifications.
Responsible for developing applying and maintaining quality standards in all work.
Key Responsibilities
AAP/EEO DFWP
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
Medical Engineering Consultants (MEC) support medical device and pharmaceutical companies to be more efficient and productive by providing resources, knowledge, and expertise to augment and supplement to their work. Our vision is to closely align our clients’ needs with the best resources available in the marketplace. We take proactive, preventative, and corrective action and create a roadmap for ongoing future improvement by identifying, integrating, and executing sustainable solutions that validate processes, ensure fully compliant quality systems, and close gaps between current and FDA expected stages.
MEC offers companies short or long-term support — from high-end leaders, managers and consultants to skill-set Engineering staff and SME’s (Subject Matter Experts).
MEC's mission is to inspire positive cultural change from within, and always exceed our clients’ expectations.
Applicants must be authorized to work in the U.S. in accordance with applicable law. This position is not eligible for employer-sponsored work authorization now or in the future.
Hybrid
Job Purpose
Develops embedded software firmware unit / integration tests firmware requirements and firmware verification tests.
Responsible for analyzing designing programming debugging and modification of an embedded software code base of a class III medical device.
May interface with cross-functional teams to define system requirements and/or necessary modifications.
Responsible for developing applying and maintaining quality standards in all work.
Key Responsibilities
- Designs develops debugs modifies tests embedded software code in C / C and Python.
- Documents software development and/or test development by writing documents reports memos change requests. Methods used are determined by approved procedures and standards.
- Tracks software development effort by creating and maintaining records in the approved tracking management tool.
- Analyzes evaluates verifies requirements software and systems by using software engineering practices.
- Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
- 5 - 13 Years with BS
- 7 - 11 Years with MS
- 4 - 8 Years with PhD
- C / C experience
- Experience in a regulated industry medical device aerospace automotive etc.
- Technical leadership and communication skills Additional Job Specific Requirements:
- Sponsorship is not available for this position
AAP/EEO DFWP
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.