Job Function: Quality
Job Sub Function: R&D/Scientific Quality
Job Category:Professional
All Job Posting Locations:Raynham, Massachusetts, 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.
About DePuy SynthesDePuy Synthes is a global leader in Orthopaedics, advancing patient care through innovative solutions across joint reconstruction, trauma, spine, sports medicine, and related surgical technologies. As DePuy Synthes separates from Johnson & Johnson to become the world's largest, most comprehensive Orthopaedics-focused company, the organization is entering a defining chapter-establishing its own corporate identity, voice, culture, and reputation while continuing to serve patients, customers, and healthcare systems around the world.
DUTIES & RESPONSIBILITIESJohnson & Johnson is recruiting for a DFI Specialist
Under general direction and in accordance with all applicable federal, state, and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
- Responsible for presenting business related issues or opportunities to next management level.
- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
- Work with NPD and LCM project teams to advise on design for inspection requirements.
- Collaborating using DFI tools as the SME for inspection, GD&T, gage design and automated inspection technologies along with strong understanding of manufacturing processes to help drive the DFI discussion during Internal and external drawing reviews.
- Troubleshoot and problem solve quality issues applying basic research and analysis techniques. Functions as technical resource and "go-to" person regarding quality issues with their specific area.
- Recommends new inspection methods as required.
- Apply knowledge and expertise to conduct training on inspection methods.
- Program and run automated inspection equipment (CMM, Keyence, Sylvac, etc)
- Works independently to complete routine and complex inspections using applicable technical documents to verify product and services conform to quality and other engineering and Quality Assurance requirements.
- Work with external vendors (travel as needed) to qualify automated and non-automated inspection methods per local procedures.
DFI Drawing Reviews- Ensure Inspectability of all dimensions
- Review GD&T and evaluate inspection requirements
- Feature criticality and gage requirements
- Accurate use of GD&T
- Provide input to project teams on alternative design structure to accommodate inspection
- Provide guidance on inspection methods
- Evaluate tolerance vs. Inspection Technique and equipment
- Ensure accurate layout of dimensions
- Verifying Datum Structure
- Accurate
- Repeatable
- Relates to the GD&T
- Ensure drawings stands on their own without interpretation of intent
- Ensure drawing views are accurate per internal and industry drawing standards
- Ensure all features are dimensioned fully and accurately
Required Skills:Preferred Skills:Agility Jumps, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Database Backup, Data Savvy, Disruptive Innovations, Issue Escalation, Problem Solving, Process Oriented, Product Improvements, Quality Control (QC), Quality Control Testing, Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing
The anticipated base pay range for this position is :$92,000.00 - $148,350.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
