Quality Engineer III
About The Position
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.
Requirements
- Bachelor of Science in Engineering.
- Minimum of 3 years' relevant experience, specifically involving process validation and verification activities and risk management documentation such as Design/Process FMEAs.
- Knowledge of basic quality systems and good documentation practices.
- Ability to work independently with limited supervision.
- Experience in the medical device field in a manufacturing support role.
- Self-starter with the ability to identify improvement opportunities.
- Knowledge of analytical techniques, problem solving, and statistical analysis.
- Proficiency with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook.
- Familiarity with product/component documentation, inspection and testing, and Manufacturing Execution Systems.
Responsibilities
- Experience leading cross-functional teams and driving projects to completion.
- Demonstrated ability to manage multiple projects spanning diverse engineering disciplines (e.g., equipment qualification, process validation, test method validation).
- Prior interactions with disciplines such as manufacturing engineering, CAPA, risk management, supplier quality, and process engineering.
- Experience providing quality support to manufacturing lines.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
