Manufacturing Quality Engineering Manager

• Job title Manufacturing Quality Engineering Manager
• Function Quality
• Sub function Quality Assurance
• Category Manager, Quality Assurance (PL7)
• Location Danvers / United States of America
• Date posted Jun 12 2026
• Requisition number R-079734
• Work pattern Fully Onsite

This job posting is anticipated to close on Jun 19 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

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.

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Job Description:

Johnson & Johnson is recruiting for a Manufacturing Quality Engineering Manager, located in 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 Manufacturing Quality Engineering Manager is responsible for leading manufacturing quality engineering activities that support regulatory compliance, production quality, and manufacturing and supply chain operations. This role provides leadership to a team of quality engineering professionals, supports robust quality systems and data-driven decision making, and partners cross-functionally to resolve quality issues, sustain manufacturing performance, and drive continuous improvement in a regulated medical device environment.

Key Responsibilities:

• Supervise Manufacturing and Supplier Quality Engineering associates and support quality metrics, reporting, and resolution of quality issues.
• Lead and support Material Review Board activities, ensuring appropriate resourcing to minimize MRB material value and reduce potential part shortages.
• Conduct external supplier audits, execute CAPA action and effectiveness activities, and support resolution of field complaints.
• Lead, manage, and assign long- and short-term tasks for the Plant Quality Engineering team, including training, development, mentoring, goal setting, and budgeting.
• Develop, improve, and maintain quality objectives, and track and trend performance against those objectives.
• Develop and improve quality data systems and provide regular quality data reporting on a global basis.
• Ensure risk-based quality processes are in place and effectively implemented across relevant areas.
• Support obsolescence programs related to suppliers and ensure appropriate quality input and oversight.
• Ensure effective quality-related communication globally, locally, and across functions inside and outside the department.
• Communicate business-related issues or opportunities to the next management level and ensure compliance with applicable Company, regulatory, Health, Safety, and Environmental requirements.

Qualifications

Education:

• Bachelor’s degree in a scientific or engineering discipline required; Master’s degree preferred.

Experience and Skills:

Required:

• Minimum of 6-8 years of related experience
• Experience in a GMP-related field within a Biotechnology, Biologics manufacturing, Medical Device, or similarly regulated manufacturing environment.
• Minimum of 5 years of experience managing and leading quality systems and associated teams at a company or corporate level.
• Experience supporting FDA, Notified Body, or other regulatory inspections or audits.
• Knowledge of global quality system and regulatory requirements, including applicable FDA regulations, ISO 13485, and other relevant standards.
• Strong knowledge of GMP, SOPs, and quality systems in a regulated manufacturing environment.
• Ability to lead multiple assignments in collaboration with department system owners and cross-functional stakeholders.
• Excellent interpersonal, verbal, and written communication skills, with the ability to work independently with scientific and technical personnel.

Preferred:

• Advanced proficiency with Microsoft Office applications and Adobe Acrobat.
• Lead Auditor, Internal Auditor, External Auditor, ASQ, Six Sigma, or related certification preferred.
• Ability to quickly understand technology, medical applications, and applicable regulations and standards.
• Demonstrated ability to create and effectively communicate regulatory and quality system expectations.
• Demonstrated ability to positively influence groups across an organization to align around a common quality philosophy.
• Ability to manage and execute multiple critical projects simultaneously in a fast-paced environment with changing priorities.
• Strong ethics and judgment, including the ability to escalate issues appropriately in the face of competing priorities.

Other:

• English proficiency (oral & written) is required.
• Travel may be required based on business needs, including potential supplier, site, or audit support.
• Certifications: Lead Auditor, Internal/External Auditor, ASQ, Six Sigma, or related certification preferred.
• Shift schedule: Standard business hours, with flexibility required to support business needs.

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.

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The anticipated base pay range for this position is :

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