What are the responsibilities and job description for the Electrical Engineer position at Medical Engineering Consultants (MEC)?
Job 2792 - Sr Electrical Engineer - Contract located in Los Angeles County
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.
Onsite
Job Purpose
Develop new manufacturing/test equipment and software used in the development and production of medical devices.
Independently or as a member of a team directs develops concepts and executes specifications designs plans and builds of complex manufacturing and test equipment.
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.
Onsite
Job Purpose
Develop new manufacturing/test equipment and software used in the development and production of medical devices.
Independently or as a member of a team directs develops concepts and executes specifications designs plans and builds of complex manufacturing and test equipment.
Key Responsibilities
- Leads or participates on project teams to develop clear specifications evaluates feasibility of concepts and provides formal estimates for electrical/software designs.
- Coordinates monitors and documents project designs estimates and costs.
- Creates electrical/software designs utilizing the departments standard development tools and procedures.
- Complete project deliverables and monitor project schedule and scope changes to assure team can meet delivery requirements.
- Prepares standard reports/documentation to communicate status and results
- Leads project teams that include Designers Engineers and Technicians in the design assembly and debug of equipment.
- Designs electrical systems and specifies electrical components.
- Identifies pneumatic components and automated control requirements.
- Completes FDA/QSR equipment requirements by assisting in the creation of specifications and qualifications.
- Provides training as required to ensure that the controls systems can be operated effectively.
- Provides leadership role on championing functional best practices.
- Influences and defines functional departmental and divisional procedures through involvement with cross-functional engineering initiatives.
- Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
- 5 - 7 Years with BS
- 3 - 5 Years with MS
- Minimum 5 Years experience per below with BS
- 3 - 5 Years with MS
- Python experience
- Electronic Hardware design experience
- Hardware-software integration experience
- Test infrastructure verification and validation experience
- Experience bridging high-level system architecture with detailed electronic hardware design
- Analytical mindset -Excellent statistical analysis -Risk Safety optimization experience
- Excellent collaboration and communications
- Medical device experience highly preferred
- Former regulated environment required
- 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.