Staff Engineer Technical Life Cycle Management (US)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Engineering

Job Sub Function:

Manufacturing Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Irvine California United States of America

Job Description:

Johnson & Johnson is currently recruiting for a Staff Engineer Technical Life Cycle Management to be based at Irvine CA with consideration for Galway IRE.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s):

(Ireland) - Requisition Number: R-059254

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery Ready to join a team thats reimagining how we heal Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the worlds most prevalent conditions such as obesity cardiovascular disease and cancer. Patients are waiting.

Your unique talents will help patients on their journey to wellness. Learn more at SUMMARY

The position requires the use of multidisciplinary engineering and supply chain knowledge to assist in the execution of cross-functional projects in support of the companys strategies goals objectives and product portfolio. Uses knowledge of scientific techniques and process excellence to design develop and validate safe effective and efficient processes. Provides technical support to ensure continuity of supply.

DUTIES & RESPONSIBILITIES

Under general supervision and in accordance with all applicable international federal state and local laws/regulations/requirements and Corporate Johnson & Johnson procedures and guidelines this position:

Execute Life Cycle Management projects in a cross-functional setting.

Work on unusually complex problems and provides solutions which are highly innovative and ingenious.

Apply scientific and engineering knowledge to the development and improvement of medical device products associated processes and manufacturing equipment as well as associated validations.

Work independently and in cross-functional teams (both internal and external) to determine root cause develop mitigations and corrective and preventative actions for processes and manufacturing related issues.

Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Evaluate manufacturing processes / products and collaborates with R&D NPI Sourcing QA MFG and Finance teams to lead projects / initiatives to improve quality productivity and reduce costs.

Utilize the application of six sigma and lean tools and methodologies.

Design and develops troubleshooting guides and decision-making matrices to ensure the standard application of methods in the resolution of process/ manufacturing technical issues.

Provide technical training and guidance to manufacturing and engineering personnel.

Ensure quality conduct of projects including design data summary and interpretation report and manuscript preparation and review compliance to applicable regulations.

Generate written reports and provide technical expertise to related projects.

Maintain accurate documentation of concepts designs drawings processes test methods data analysis and conclusions or rationales.

Provide technical support for outside suppliers vendors and/or consultants as required inclusive of supplier visits and identification / implementation of process improvements.

Provide guidance and work direction to lower-level engineers and related project team members.

Responsible for communicating business related issues or opportunities to next management level.

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 International Federal State local and Company regulations requirements policies and procedures.

Performs other duties assigned as needed.

EDUCATION

A minimum of a Bachelors degree is required.

REQUIRED SKILLS

A minimum of 10 years of professional experience.

Familiarity with ISO 13485 Design Control and manufacturing process IQ OQ PQ qualifications as related to medical devices.

Knowledge in some special processes such as polymer processing (compounding extrusion fusing) metal processing (machining laser cutting polishing) welding coil winding equipment & tool design

Strong project management skills required (Microsoft Project FPX and/or other project management tools).

A highly regulated industry knowledge.

Six Sigma Process Excellence knowledge is required with certification at the Black belt level preferred.

Knowledge of Design for Manufacturability in plastics metals and small scale assembly process.

Strong communication team buidling and cross functional coordination skills.

A Working knowledge of applicable requirements related to the MDSAP jurisdiction.

PREFERRED SKILLS

An advanced degree.

Previous supervisory experience.

PMP certification or equivalent

Medical device industry experience.

Process automation knowledge for small scale assembly.

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.

Required Skills:

Preferred Skills:

Accelerating Coaching Critical Thinking Facility Management Good Manufacturing Practices (GMP) Lean Manufacturing Principles Lean Supply Chain Management Manufacturing Engineering Performance Measurement Product Design Program Management Project Engineering Project Schedule Risk Compliance Robotic Automation Safety-Oriented Science Technology Engineering and Math (STEM) Application Technologically Savvy

The anticipated base pay range for this position is :

$109000.00 - $174800.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).
For additional general information on Company benefits please go to: - position is eligible to participate in the Companys 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