Job Details

ID #15470266
Estado California
Ciudad Irvine
Tipo de trabajo Contract
Salario USD Competitive Competitive
Fuente Ledgent Technology
Showed 2021-06-15
Fecha 2021-06-14
Fecha tope 2021-08-13
Categoría Etcétera
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Sr. Software Validation Engineer

California, Irvine, 92614 Irvine USA

Vacancy caducado!

Roth Staffing is looking for a r. Software Validation Engineer within the medical technologies firm for our client in Irvine, CA. This is an exciting opportunity to work for a global leader in life-saving medical devices with a strong corporate culture and competitive pay.

Key Responsibilities: Resources(s) are required to represent the Software Verification and Validation (V&V) group on new product development teams. Primary responsibility will be to create and execute Test Cases during a Sprint. Coordination with onsite and offshore resources will be necessary. Assertive and takes initiative, has excellent understanding of Sprints/ Agile methodology, and will have had experience developing and/or testing software systems. Experience developing and/or testing medical devices that contain embedded software. Represent the Software V&V group on an Agile team Manage the Boards and Tasks pertinent to the V&V group in Azure DevOps Review, analyze and provide feedback on User Stories and Software Requirements Create and execute Test Cases in Sprints Review test results Establish traceability between requirements and test cases Raise and manage defects with the QA group Coordinate with offshore resources.

Skills Good leadership skills and ability to influence change Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on contracts or projects Ability to manage competing priorities in a fast-paced environment and work independently, with minimal direction Ability to interact professionally with all organizational levels Strong problem-solving, organizational, analytical and critical thinking skills Strong documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills Proven expertise in usage of MS Office Suite including MS Project; CAD experience required Basic understanding of statistical techniques Previous experience working with lab/industrial equipment required Substantial understanding and knowledge of principles, theories, and concepts relevant to Engineering Substantial understanding of processes and equipment used in assigned work Knowledge of applicable FDA regulations for medical device industry Strict attention to detail Adhere to all corporate rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.

Education/Experience Bachelor's Degree in Engineering or Scientific field with 4 years of experience including either industry or industry/education Required OR Master's Degree or equivalent in Engineering or Scientific field with, 3 years of experience including either industry or industry/education Required OR Ph.D. or equivalent in Engineering or Scientific field with industry experience or industry/education Required.

We are an equal opportunity employer and make hiring decisions based on merit. Recruitment, hiring, training, and job assignments are made without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, or any other protected classification. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Vacancy caducado!

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