DIRECTOR SUPPLY CHAIN QUALITY BUSINESS LEAD WCH & BIOSURGERY

Ethicon, a member of Johnson & Johnson Family of Companies, is recruiting a Director Supply Chain Quality Business Lead WCH & Biosurgery to be located in Raritan, NJ; Raynham, MA; San Angelo, TX; Cornelia, GA and/or San Lorenzo, PR.
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.
nj.
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The Director Supply Chain Quality Business Lead serves as the connection with the Supply Chain Quality partners at WCH & Biosurgery site Quality leads and Source Quality leads to ensure deployment of continuous improvement activities.
The Supply Chain Quality Business Leader will ensure that we are better aligned to support the needs of the business, ultimately helping to transform the way we serve customers and patients with high-quality and compliant products each and every day into the future.
The Director is responsible to maintain a connection with the Quality Centers of Excellence through strategies that drive continuous quality excellence, maintain supply chain compliance, providing platform (Ethicon Wound Closure and Healing and Biosurgery) support and addressing customer facing needs.
In addition, this leader will identify and implement key capabilities that will make Quality a competitive advantage by unlocking efficiency and accelerating execution.
This role has organizational responsibility for budget, governance and project coordination and at time, direct management of projects.
The European Logistics Center Manager will report to this role and with that, overall legal entity oversight and strong connection to Ethicon LLC Quality Management System leader.
Are you interested in joining a diverse team delivering outstanding results to our customers? Apply now for this exciting opportunity! Key Responsibilities.
Serve as the single point of contact for Quality Centers of Excellence in all of the End to End platform/franchise forums developing and driving End to End Supply Chain Quality strategies.
Collaborate with other Quality and Supply Chain partners in identifying and deploying platform end to end strategies associated with Service, Quality, Compliance and People enabling platform Strategic Plans and Long-Range Financial Planning Ensure that all processes needed to operate both the Legal entities including implementation of EU MDR are established, implemented, and maintained.
Support the resolutions of platform issues associated with QMS, Compliance, Remediation & Audit Strategies.
Maintain and lead overall budget for Ethicon WCHB SCQ budget including routine reporting for all WCHB manufacturing sites, Source Quality and home office/admin budgets, LRFP, JU, NU and BP preparation and presentations.
Provide overall governance and organization for Ethicon WCHB SC Quality organization including G&O preparation and review, staff meetings, budget and project reviews.
Provide oversight and direct project management as directed by the Ethicon WCH SC Quality Leader.
Strong connection to WCHB Strategy & PMO group/leaders, SC Quality Network Optimization teams.
Delegate of the Sr.
Supply Chain Quality Director.
Maintain access to appropriate Quality System platforms in order to complete approvals as needed (e.
.
ETQ, Adaptiv, etc.) Follow all environmental, safety and occupational health policies (i.
., ISO & OSHAS ) Responsible for presenting business or quality related issues or opportunities to next management level, assisting site teams with these decisions and investigations as needed.
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.
Qualifications Education.
A minimum of a Bachelor’s degree in a Life Science, Engineering, Physical Science or related field is required.
Experience and Skills.
Required.
A minimum of ten (10) years of related experience and/or training in a regulated environment.
A minimum of five (5) years of active management experience, including direct supervision and matrix management.
General knowledge of e-mail, word processing, spreadsheets, and presentations.
Strong communication, influencing and leadership skills.
Ability to communicate at all levels of the organization, project management and problem solving.
Preferred.
Manufacturing site experience in manufacturing, business excellence or quality Experience in the Medical Device industry or medical field Knowledge of ISO and QSR/EU MDD-MDR regulations Key front-room role experience with FDA (or similar) inspection and Notified Body inspections Other.
Project management and Lean Six Sigma Black Belt certifications are preferred.
This position may require up to 25% domestic & international travel.
Weekend travel and work, and participation in conference calls and meetings during late night/early morning hours may be required occasionally.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
The anticipated base pay range for this position is $ to $.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs.
medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be 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.
Employees are eligible for the following time off benefits.
Vacation – up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year Holiday pay, including Floating Holidays – up to 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year For additional general information on Company benefits, please go to.
https://www.
areers.
nj.
om/employee-benefits This job posting is anticipated to close on .
The Company may however extend this time-period, in which case the posting will remain available on https://www.
areers.
nj.
om to accept additional applications.  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.
areers.
nj.
om.