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Job Function: Supply Chain Engineering
Job Sub Function: Quality Engineering
Job Category:Scientific/Technology
All Job Posting Locations:Warsaw, Indiana, United States of America
Job Description:Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
DePuy Synthes Companies is a member of Johnson & Johnson's Family of Companies and is recruiting for an
Engineer I, Source Quality to belocated in
Warsaw, IN.
About MedTechFueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at ;br>
DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit ;br>
Key Responsibilities:Under the direction of a Sr. Engineer, the Engineer I,
- Provides quality engineering leadership in the management of select External Manufacturers, Direct Material, and Indirect material suppliers.
- Responsible for technical leadership in establishing quality expectations at the supplier.
- Implements, and/or maintains, production and process controls using appropriate techniques (for example, process capability measures, statistical process controls, process performance metrics).
- Partner with product development teams to support successful launches at suppliers.
- Conduct supplier visits emphasizing quality improvement and compliance with good manufacturing practices, ISO-13485 and other applicable standards.
- Provide Quality Engineering support to suppliers including inspection technique support, product non-conformances, verification/validation activities.
- Contributes to root cause investigations using various problem-solving techniques and tools, and assesses corrective action effectiveness.
- Applies various risk management and risk mitigation tools and practices (for example, mistake proofing, critical control points, failure mode, effects analysis).
- Communicate at all levels within Quality and across functions or departments such as R&D, Regulatory, Manufacturing, and Marketing.
Responsibilities:QualificationsEducation:- A minimum of a Bachelor's or equivalent university degree in Engineering or related Scientific focus is required
Experience and Skills:Required:- 0-2 years of related experience
- Excellent problem solving and decision-making skills
- Communication/Interpersonal skills and flexibility to enable resolution of technical situations
Preferred:- Relevant work, internship, or Co-Op experience
- Experience or knowledge with manufacturing processes; machining, injection molding, additive manufacturing and/or electronics manufacturing
- Medical Device and/or Pharmaceutical industry
- Six Sigma, Lean, or ASQ Certification/training
- Quality engineering experience
- Experience with Blueprint reading/literacy including GD&T
- Familiarity with inspection methods and techniques
- Knowledge of FDA CFR Part 820 and ISO 13485
- Experience with process validation
Other:- This position may require up to 25% travel
Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via Internal employees contact AskGS to be directed to your accommodation resource.
#LI-Hybrid Required Skills: Preferred Skills:Customer Centricity, Data Savvy, Document Management, Execution Focus, Good Automated Manufacturing Practice (GAMP), Issue Escalation, Lean Supply Chain Management, Process Control, Process Improvements, Quality Control (QC), Quality Services, Quality Standards, Quality Systems Documentation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy
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