What are the responsibilities and job description for the Electrical Engineer position at Medical Engineering Consultants (MEC)?
Job 2736 - Mid Level 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 - Possible extension
Job Purpose
This is a high execution role. Person will be working with Senior Engineers.
Key Responsibilities
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Qualifications
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 - Possible extension
Job Purpose
This is a high execution role. Person will be working with Senior Engineers.
Key Responsibilities
- Identifying gaps in the acquired company's compliance to our client's Work Instructions and SOPs and defining strategy to close these gaps.
- Providing input to project goals and progress and recommending appropriate revisions.
- Communicating progress, risks and trade-offs of technical deliverables to project leadership and recommends revisions as needed.
- Completing complex or novel assignments requiring the development of new or improved techniques and procedures.
- Work is expected to result in efficient and effective integration of medical device technologies to our client's portfolio.
- Successfully completing engineering work in electrical design remediation, product design refinement, preparation of specifications, test method validation and report preparation.
- Assessing the feasibility and soundness of alternative engineering processes, products or equipment.
- Contributing to design hazard analysis FMEA and ensuring compliance with our client's design control and risk management standard operating procedures.
- Completing clear and concise engineering documentation to facilitate knowledge transfer during product integration.
- Collaborating with external partners and suppliers to align component specifications qualification and acceptance activities testing protocols and quality standards.
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Qualifications
- BS or above in Electrical Engineering or related field
- 4 years of engineering experience with bachelor's degree or 2 years with Masters
- Strong electrical and/or systems engineering design documentation experience, problem-solving skills and attention to detail
- Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources
- Strong written and verbal communication, judgment, decision-making, collaboration and critical thinking skills
- Personal drive, individual accountability, a strong bias for action.
- Must have medical device experience preferred
- Must have worked in regulated field
- Implantable medical device experience and testing highly preferred
- Strong electrical and/or systems engineering design documentation experience problem-solving skills and attention to detail
- Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources
- Strong written and verbal communication, judgment, decision-making, collaboration and critical thinking skills
- Personal drive, individual accountability, a strong bias for action.
- Familiarity with IEC 14708 and 45502 Active Implantable standards
- Familiarity with IEC 60601 Electrical Medical Equipment standards
- Experience in Test Fixture Design and Implementation
- Experience in Analog and Digital Design
- Experience using LTspice or equivalent Electrical Simulator Tools
- Experience in Altium for Schematic Capture and PCB Design
- Experience in RF Design and Test
- Experience in Hands-on Electronics Troubleshooting
- Experience in medical device Design Acceptance and Design Verification testing
- Ability to build strong relationships across the organization and with external stakeholders
- 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.