Overview
On Site
Depends on Experience
Contract - W2
Contract - 12 Month(s)
Skills
ivd
invitro
in vitro
in-vitro
Job Details
Job Title: Senior Systems Engineer
Location: Santa Clara, CA
Onsite Position
Summary:
This Senior Systems Engineer will be part of the System Development team focusing on the development of client's IVD automated systems and end-to-end product solutions. The individual is expected to provide technical and process expertise in collaboration with internal stake holders and cross functional teams throughout total product development lifecycle to develop and maintain medical device products, according to customer requirements, applicable regulatory and quality standards. This role is expected to lead and mentor less experienced engineers and their career development.
Responsibilities:
This position is responsible for, but not limited to, the following:
You re someone who wants to influence your own development. You re looking for a company where you have the opportunity to pursue your interests across functions and geographies.
Where a job title is not considered the final definition of who you are, but the starting point.
Qualifications:
This Senior Systems Engineer will be part of the System Development team focusing on the development of client's IVD automated systems and end-to-end product solutions. The individual is expected to provide technical and process expertise in collaboration with internal stake holders and cross functional teams throughout total product development lifecycle to develop and maintain medical device products, according to customer requirements, applicable regulatory and quality standards. This role is expected to lead and mentor less experienced engineers and their career development.
Responsibilities:
This position is responsible for, but not limited to, the following:
- Provide technical expertise to cross-functional teams to develop IVD systems and ensure the product design will meet customer requirements as well as applicable standards and regulations;
- Develop and manage systems level product requirements;
- Perform product risk management activities;
- Develop and execute verification/validation activities and traceability analysis;
- Create artifacts required for project deliverables;
- Resolve issues found according to company s defect/change tracking process;
- Maintain knowledge of current regulatory requirements and standards as they pertain to the development and testing of medical/IVD devices;
- Maintain compliance as required by regulatory bodies and the company s quality system;
- Collaborate with cross functional teams to identify opportunities for continuous process improvement;
- Lead and mentor less experienced Systems Engineers;
- Support FDA and other regulatory submission and audits;
You re someone who wants to influence your own development. You re looking for a company where you have the opportunity to pursue your interests across functions and geographies.
Where a job title is not considered the final definition of who you are, but the starting point.
Qualifications:
- Bachelor s degree in Systems Engineering, Biomedical Engineering, Electrical Engineering or related disciplines. Advanced degree preferred;
- 5+ years of professional experience in the medical device industry. Experience in IVD industry highly desirable;
- Hands-on experience with liquid pipetting systems such as Hamilton, Tecan etc. is a plus;
- Experience developing product requirements and design inputs;
- Experience conducting risk management activities per ISO 14971;
- Strong analytical, problem solving, communication, and interpersonal skills;
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.