Engineer, Process Engineering

Johnson & Johnson MedTech

Danvers (MA)

On-site

USD 65,000 - 105,000

Full time

14 days+

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Benefits offered by this job

Annual bonus
Health/dental/vision insurance
Paid time off

Job summary

Johnson & Johnson, a leader in cardiovascular and medical device innovation, is seeking an Engineer in Process Engineering within the Supplier Engineering function. This role provides operational and technical support to ensure compliant quality, testing, documentation, and change management across engineering programs.

You will coordinate testing, documentation, and cross-functional activities, enabling engineers to focus on core technical work while adhering to procedures and regulatory

Qualifications

  • Technical degree, technician qualification, or equivalent practical experience in engineering, manufacturing, or quality.

Responsibilities

  • Supports Supplier Engineering through execution and coordination of operational and technical activities related to quality, testing, documentation, and change management.
  • Maintains and updates quality and engineering systems (e.g., Non-Conformances, Quality Inspection Plans, Change Requests), ensuring data accuracy, completeness, and compliance.
  • Supports non-conformance and quality processes, including documentation preparation, investigation support, and facilitation of Material Review Board activities.
  • Coordinates and executes testing and qualification support activities, including sample handling, measurement, data collection, test documentation, and test build organization.
  • Organizes and tracks engineering-related logistics such as samples, assemblies, and shipments to ensure availability for testing and qualification activities.
  • Prepares, updates, and maintains technical documentation, including protocols, reports, and engineering records.
  • Supports change control processes by preparing documentation, performing system entries, and tracking progress to ensure timely execution.
  • Executes defined work packages and routine technical tasks with a high degree of accuracy and independence within established procedures.
  • Identifies opportunities for process improvements and contributes to standardization and efficiency initiatives within Supplier Engineering.
  • Collaborates cross-functionally with Engineering, Quality, Manufacturing, and Supply Chain.
  • Responsible for communicating business related issues or opportunities to next management level.

Skills

Engineering coordination
Quality systems
Documentation
Cross-functional collaboration
Problem solving
Independent work

Education

Technical degree or equivalent

Tools

ETQ
SAP

Job description

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

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Danvers, Massachusetts, United States of America

Job Description

We are searching for the best talent for Engineer, Process Engineering

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

Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Position Summary

This position provides operational and technical support to the Supplier Engineering function to ensure efficient execution of quality, testing, documentation, and change management activities. The role focuses on executing structured engineering support tasks, maintaining system and documentation integrity, and coordinating operational activities such as testing, logistics, and non-conformance handling. By taking ownership of routine and process-driven tasks, this role enables Supplier Engineers to focus on core technical and strategic responsibilities while ensuring compliance with internal procedures and regulatory requirements in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines.

Responsibilities
  • Supports Supplier Engineering through execution and coordination of operational and technical activities related to quality, testing, documentation, and change management
  • Maintains and updates quality and engineering systems (e.g., Non-Conformances, Quality Inspection Plans, Change Requests), ensuring data accuracy, completeness, and compliance
  • Supports non-conformance and quality processes, including documentation preparation, investigation support, and facilitation of Material Review Board activities
  • Coordinates and executes testing and qualification support activities, including sample handling, measurement, data collection, test documentation, and test build organization
  • Organizes and tracks engineering-related logistics such as samples, assemblies, and shipments to ensure availability for testing and qualification activities
  • Prepares, updates, and maintains technical documentation, including protocols, reports, and engineering records
  • Supports change control processes by preparing documentation, performing system entries, and tracking progress to ensure timely execution
  • Executes defined work packages and routine technical tasks with a high degree of accuracy and independence within established procedures
  • Identifies opportunities for process improvements and contributes to standardization and efficiency initiatives within Supplier Engineering
  • Collaborates cross-functionally with Engineering, Quality, Manufacturing, and Supply Chain
  • Responsible for communicating business related issues or opportunities to next management level
  • Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
  • For those who supervise or manage a staff, 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
  • Performs other duties assigned as needed
Qualifications
  • Technical degree, technician qualification, or equivalent practical experience in engineering, manufacturing, or quality
  • 1–5 years of experience in a manufacturing, engineering, or quality environment
  • Familiarity with engineering support, quality processes, or production environments is advantageous
  • Basic understanding of technical drawings, specifications, and manufacturing processes
  • Knowledge of quality system processes such as Non-Conformance (NC), CAPA, or inspection processes
  • Strong organizational and coordination skills with attention to detail
  • Ability to manage multiple tasks and maintain structured documentation
  • Strong communication and collaboration skills across functions
  • Ability to work independently on defined tasks and take ownership of assigned activities
  • Problem-solving mindset with focus on continuous improvement
Preferred
  • Experience working with electronic systems (e.g., ETQ, SAP, eMP, Lynx or similar) preferred
  • Experience in medical device or regulated industry is preferred

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 under 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, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is: $65,000 - $ 104,650

Benefits
  • The Company maintains highly competitive, performance-based compensation programs.
  • Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan.
  • The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year.
  • Bonuses are awarded at the Company’s discretion on an individual basis.
  • 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 (401k).
  • 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.careers.jnj.com/employee-benefits

This job posting is anticipated to close on August 28, 2026. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

Required Skills
Preferred Skills

Analytical Reasoning, Computerized Equipment Skills, Corrective and Preventive Action (CAPA), Emerging Technologies, Execution Focus, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Process Control, Process Engineering, Process Oriented, Product Improvements, Project Engineering, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy

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