Quality Engineering Senior

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. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Supply Chain Engineering

Quality Engineering

Scientific/Technology

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. Supplier Quality Engineer to be located in Palm Beach Gardens, FL .

Your unique talents will help patients on their journey to wellness. Implement SQ strategy and follow Supplier Quality standards

Support QE with supplier product PVE’s (First Article Inspection, Control Plans, Critical to Quality, Capability studies)

Contribute to product investigations related to product and process complaints.

Provide Supplier Quality Engineering support for PLM changes.

Support supplier preparation for inspections by authorities/third parties

Support Procurement executing supplier transfer projects

Support for Quality Agreement and Change Agreements, supplier assessments and supplier audit process

Report on supplier performance metrics and management reviews.

Lead or participate in Quality projects: Implementation of improved/new standards for supplier quality

Responsible for following all company guidelines related to Health, Safety and Environmental practices as applicable.

Responsible for ensuring that subordinates follow all company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable

Responsible for ensuring personal and company compliance with all Federal, State, local and Company regulations, policies, and procedures

May directly or indirectly supervise and/or provide directions to other Supplier Quality Engineers.

Collaborate with other functional departments such as Quality, Engineering, R&D, Regulatory and Sourcing

May interact with government agencies such as the FDA, Regulatory Agencies such as Notified Bodies and will interact with suppliers providing products and services that could impact the quality of J&J products

Bachelor's or equivalent university degree is required; A concentration in Engineering, Life Science, or related field is preferred

Strong root cause analysis skills

Ability to communicate verbally and in writing

Experience in the medical device and/or pharmaceutical industry

Experience or knowledge with machining manufacturing processes, injection molding, robotics, electronics and/or software

Operations supplier quality experience

Fluency (oral & written) in English is required

Up to 10% travel may be required

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.

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.

Analytical Reasoning, Coaching, Customer Centricity, Data Savvy, Document Management, Financial Competence, Good Automated Manufacturing Practice (GAMP), Lean Supply Chain Management, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy

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