Director, Bioresearch Quality Process Management
Company: 6084-Janssen Research & Development Legal Enti
Location: Brunswick
Posted on: April 1, 2026
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Job Description:
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
jnj.com 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:
Quality Job Sub Function: Multi-Family Quality Job Category: People
Leader All Job Posting Locations: Cincinnati, Ohio, United States
of America, Danvers, Massachusetts, United States of America,
Irvine, California, United States of America, Jacksonville,
Florida, United States of America, Miami, Florida, United States of
America, Mountain View, California, United States of America, New
Brunswick, New Jersey, United States of America, Palm Beach
Gardens, Florida, United States of America, Raritan, New Jersey,
United States of America, Santa Clara, California, United States of
America Job Description: Johnson & Johnson is recruiting for a
Director, Bioresearch Quality Process Management , located at one
of the identified Johnson & Johnson Medtech sites: New Brunswick,
NJ; Mountain View, CA; Cincinnati, OH; Jacksonville, FL; Miami, FL;
Raritan, NJ; Irvine, CA; Palm Beach Gardens, FL; Santa Clara, CA
and Danvers, MA. About MedTech Fueled 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 https://www.jnj.com/medtech The Director,
Bioresearch Quality Process Management, is a highly experienced and
strategic leader accountable to spearhead Bioresearch related
quality process enhancements and governance. In partnership with
MedTech Bioresearch R&D Quality functional leads and MedTech
Q&C Centers of Excellence, this critical role is instrumental
in enabling transparency of bioresearch quality risks across
MedTech Business Units, with fit for purpose and standardized
quality processes & approaches in support of pre-clinical,
clinical, medical safety and pharmacovigilance quality program
activities. The role will also ensure compliance with regulatory
standards, enhancing product quality, and leading continuous
process improvement across the organization. Critical capabilities
and experiences include strategic risk governance, stakeholder
engagement, process excellence, risk management, and people
management. The Director will enable standardization for
excellence, efficient and effective leverage of centralized
services, drive end-to-end BU line of sight to risk areas, cross BU
risk sharing and deployment of improvement strategies. Key
Responsibilities: Leadership & Strategy: Directly responsible and
accountable for supervision and development of direct reports.
Develop and implement an integrated bioresearch quality strategy
that aligns proactive risk management and MedTech organizational
goals to enable process optimization and innovation. Lead the
quality process management team to promote a culture of quality and
continuous improvement. Strategic oversight of activities and
functions responsible for providing centralized visibility and
reporting on risk data reporting. Regulatory Compliance: Ensure
MedTech R&D Quality Bioresearch procedures comply with industry
regulations (e.g., FDA, ISO) and internal policies. Bioresearch
Quality Process Management: Design and optimize scope of
Bioresearch R&D Quality processes and drive risk insights,
including Clinical Risk Management, Bioresearch Audits,
NC/CAPA/Escalation through cross-functional collaboration within
R&D Quality MedTech Bioresearch, MedTech Q&C functions,
Subject Matter Experts and cross functional business partners.
Identify areas of improvement and implement best practices
including business development due diligence, clinical risk
management, integration and inspections for bioresearch quality.
Responsible for driving innovation and continuous improvement in
portfolio bioresearch quality activity processes. Data Analytics,
Reporting & Governance: Establish and utilize data analytics
through digitalization and AI to monitor quality metrics and drive
decision-making of bioresearch quality activities. Prepare reports
for senior management on quality performance and improvement
initiatives. Enable cross Business Unit governance of bioresearch
quality risks, mitigations and sharing of best practices. Training
& Development: Oversee the development of training programs for
staff on bioresearch quality processes and compliance requirements
to ensure a knowledgeable workforce. Establish and enable sharing
of best practices through communities of practice across MedTech
Businesses. Risk Management: Establish potential risks in
pre-clinical/clinical/Med Safety/PV quality systems and processes
and implement mitigation strategies to minimize impact and drive
innovation. Responsible for owning the process to provide
centralized insights on risks, on portfolio quality activities, and
reporting processes. Stakeholder Management: Establish and maintain
strong relationships with internal and external stakeholders to
advocate for Bioresearch quality and process excellence. Portfolio
& Budget Management: Establish process for visibility to activity
drivers and portfolio. Ownership of creating and maintaining
central visibility for budget planning, prioritization and value
creation. Qualifications Education: Bachelor’s or equivalent
university degree is required Experience and Skills: Required: A
minimum of 10 years working in regulated environments Ability to
effectively apply project management tools and lean methodologies
when leading projects and programs Excellent leadership skills,
self-starting/motivated with highly developed interpersonal and
teamwork skills Ability to quickly process and communicate complex
information and make critical decisions with limited information
Experience with strategy execution and implementation, and
reporting to executive level leadership Experience influencing or
persuading others to accept new ideas, approaches, or concepts or
gains alignment on divergent issues with limited guidance
Experience with Integrations, Clinical quality processes and
procedures and systems, including remediation efforts Established
trusted leadership, anticipating business needs and proactively
takes actions; leverages relationships; develops strategic
alliances Big picture orientation with attention to detail and
results oriented Ability to work in a matrix and multi-cultural
environment Preferred: Leadership in digitalization initiatives and
AI application/products Established expertise or experience in
process excellence or design, clinical risk management, and process
management Other: Travel availability up to 20% (domestic and
international) is required English language proficiency (written
and verbal) is required 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
https://www.jnj.com/contact-us/careers . Internal employees contact
AskGS to be directed to your accommodation resource. Required
Skills: Preferred Skills: Budget Management, Compliance Management,
Corrective and Preventive Action (CAPA), Developing Others,
Inclusive Leadership, Internal Auditing, ISO 9001, Leadership,
Operations Management, Performance Measurement, Quality Control
(QC), Quality Processes, Quality Standards, Quality Validation,
Resource Planning, Risk Management, Standard Operating Procedure
(SOP), Tactical Planning The anticipated base pay range for this
position is : $150,000.00 - $258,750.00 For Bay Area: $172,000.00 -
$297,850.00 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
Keywords: 6084-Janssen Research & Development Legal Enti, Taylor , Director, Bioresearch Quality Process Management, Healthcare , Brunswick, Michigan