Job Details

ID #53383318
Estado California
Ciudad Irvine
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2025-02-01
Fecha 2025-02-02
Fecha tope 2025-04-03
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Software Quality Engineer

California, Irvine, 92602 Irvine USA
Aplica ya

About Us: Our Client is a leader in the medical device industry, committed to delivering innovative solutions that enhance patient care. We are looking for a highly skilled and motivated Software Quality Engineer to join our dynamic team. In this role, you will ensure the highest standards of software quality and compliance across multiple new product development projects.Job Description:Responsibilities:

Ensure software quality and compliance throughout the product development lifecycle, from concept and feasibility to commercialization.

Collaborate with the software core team to oversee development efforts and ensure adherence to quality standards.

Conduct software validation and verification activities to ensure product reliability and performance.

Perform root cause analysis and implement corrective and preventive actions (CAPA) to address quality issues.

Develop and execute software testing plans, including automated testing using Python frameworks.

Maintain and improve quality assurance processes and documentation in compliance with medical device regulations.

Work closely with suppliers to ensure quality standards are met and maintained.

Skills and Qualifications:

Proven experience in quality assurance, software validation, and quality engineering, particularly in the medical device industry.

Strong knowledge of software quality assurance practices and root cause analysis.

Familiarity with Python automation frameworks, C, and C#.

Experience with version control systems such as Git and Azure DevOps (ADO).

Excellent problem-solving skills and attention to detail.

Strong communication and teamwork abilities.

Preferred Skills:

Experience with supplier quality management and validation processes.

Knowledge of regulatory standards and compliance requirements for medical devices.

Familiarity with quality control methodologies and software testing techniques.

Experience Level:

Intermediate Level

Pay and BenefitsThe pay range for this position is $70.00 - $90.00/hr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Irvine,CA.Application DeadlineThis position is anticipated to close on Feb 10, 2025.About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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