Senior New Product Development Quality Engineer - Johnson and Johnson

DePuy Synthes Joint Reconstruction, a member of Johnson & Johnson Family of Companies, is recruiting a New Product Development (NPD) Quality Engineer 3 to be located in Raynham, MA!

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ .

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The New Product Development (NPD) Quality Engineer 3. This role provides Quality Engineering support to New Product Development specifically in the areas of Design Controls and Design Transfer to Manufacturing including, but not limited to: Risk Management, Design Verification and Validation Strategies, and Design Transfer to Manufacturing.

Are you interested in joining a diverse team delivering outstanding results to our customers? Apply now for this exciting opportunity!
Key Responsibilities:

• Independently provide direction and oversight of the product development quality activities across assigned projects.
• Apply various tools and methods (for example, Six Sigma, Lean) to identify and realize new product or process introductions as well as process improvements.
• Apply various risk management and risk mitigation tools and practices, for example, mistake proofing, critical control points, failure mode and effects analysis.
• Supports the reliability assessments of product design.
• Contributes to root cause investigations using various problem-solving techniques and tools and assesses effectiveness of corrective actions.
• Conducts, and supports the development of, test methods in equipment, process, and product qualifications/validations.
• Ensures that process Quality control plans are in accordance with product risk level and are consistently followed.
• Implements and/or maintains, production and process controls using appropriate techniques (for example, process capability measures, statistical process controls, and process performance metrics).
• Participates in technical reviews as appropriate.

Education:

• A minimum of a Bachelor's degree is required. Focus degree in Engineering or related technical/scientific field is preferred.

Experience and Skills:

Required:

• A minimum four (4) years of related work experience.
• Strong knowledge of Quality Engineering/Scientific methods and techniques.
• Strong knowledge of GD&T and inspection methodologies.
• Experience with a proven track record of implementing appropriate risk mitigation.
• Demonstrated leadership managing projects or improvements of varying levels of complexity and priority.
• Strong communication skills and teamwork skills to support partnering cross functionally.

Preferred:

• Technical training and experience using Statistics, Lean and Six Sigma Methodologies is preferred including Measurement System Analysis, SPC, DOEs, Reliability, etc.
• Experience working in both an FDA and European regulatory environment is preferred.
• Robust knowledge and experience supporting process qualifications.
• Quality Engineering/Design or Process Excellence/Lean experience.
• Experience with internal or external audits.
• Excellent negotiation, decision-making, and interpersonal skills that cultivate conflict resolution as it relates to technical situations.
• Demonstrated leadership skills with providing guidance and mentorship to support peers.

Other:

• This position will be located in Raynham, MA and may require up to 10% domestic or international travel.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .