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Job Details

Senior Quality Engineer

Type

Full time

Category

Engineering

Location
USA - California – Irvine
Job reference

Req-45372

Posted for

1 month ago

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Senior Quality Engineer position is a unique career opportunity that could be your next step towards an exciting future.

This role is responsible to implement and integrate new technologies and processes within Irvine Implant Manufacturing working in collaboration with external stake holders at Implant Network Level. This role is responsible to provide Quality Engineering expertise to evaluate and qualify next generation equipment and/or automation in processes, define validation and regulatory strategies/requirements, lead/own validation and qualification activities, implement new process/system integration changes, and provide training to the stake holders.


How You'll Make an Impact:

  • Identify and evaluate new technologies and process improvement ideas, lead/drive qualification and validation deliverables for the projects, implement and stabilize the new process/technology in the production environment working on the production floor.

  • Identify and ensure the optimization of complex Manufacturing and/or R&D processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk.

  • Investigate complex manufacturing product quality and compliance issues (e.g., CAPA, nonconformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.

  • Develop, update, and maintain technical content of risk management files

  • Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes

  • Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinate technician work.

  • Train, coach, and guide lower level employees on routine procedures


What You'll Need (Required):

  • Bachelor’s degree in Engineering or a related field with 4 years of relevant industry experience

  • Master’s degree with 3 years of related industry or industry/education experience.


What Else We Look For (Preferred):

  • Previous experience working with process improvements, new equipment/process qualifications in the medical device manufacturing environment, and/or new product or process qualification projects.

  • Proven expertise in usage of MS Office Suite; CAD experience preferred

  • Strong documentation, communication and interpersonal relationship skills including negotiating and relationship management skills

  • Working knowledge and understanding of statistical techniques

  • Substantial understanding and knowledge of principles, theories, and concepts relevant to Engineering

  • Strong problem-solving, organizational, analytical and critical thinking skills

  • Substantial understanding of processes and equipment used in assigned work

  • Good leadership skills and ability to influence change

  • Knowledge of and adherence to Quality systems

  • Strict attention to detail

  • Ability to interact professionally with all organizational levels

  • Ability to manage competing priorities in a fast paced environment

  • 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 interact with senior internal and external personnel on significant matters often requiring coordination between organizations

  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) 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

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California, the base pay range for this position is $108,000 to $153,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).  Applications will be accepted while this position is posted on our Careers website.  

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About Edwards Lifesciences

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.

Aviso importante para las candidatas

Aviso importante para las candidatas

Requisito de vacunación COVID

Edwards se compromete a cumplir con los requisitos y orientaciones de nuestras autoridades gubernamentales y a proteger a nuestros pacientes vulnerables y a los proveedores de atención sanitaria que los tratan en todo el mundo. Como tal, todos los puestos de trabajo que interactúan con la atención sanitaria requieren la vacunación COVID-19, lo que incluye a cualquier persona que interactúe directamente con los pacientes y a aquellos que interactúan con los proveedores de atención sanitaria como parte de su función. En caso de ser contratado, como condición para el empleo, se le pedirá que presente una prueba de que se ha vacunado completamente contra la COVID-19 o que tiene una exención religiosa o médica válida para no vacunarse. Este requisito de vacunación no se aplica en los países en los que está prohibido por ley imponer la vacunación. En los países en los que las vacunas están menos disponibles, o en los que existen otros requisitos, podemos instituir medidas alternativas que optimicen la seguridad del paciente y del personal sanitario, que pueden incluir pruebas periódicas de COVID o requisitos específicos de enmascaramiento.

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