Sr. Quality Engineer

Johnson & Johnson Co.

Woburn (MA)

On-site

USD 79,000 - 128,000

Full time

7 hours ago
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Benefits offered by this job

Vacation – 120 hours/year
Sick time – 40 hours/year
Holiday pay – 13 days/year
Parental Leave – 480 hours/year
Volunteer Leave – 32 hours/year

Job summary

Johnson & Johnson is seeking a Sr. Quality Engineer to support manufacturing of life-saving medical devices at the Danvers, MA and Woburn, MA sites. You will drive quality systems, risk assessment, and continuous improvement to ensure product safety and regulatory compliance.

The role requires 2–4 years in quality engineering, proficiency with IQ/OQ/PQ validation, and a proactive, collaborative approach across functions. This position is based in Massachusetts with cross-site responsibilities.

Qualifications

  • Bachelor’s degree in Engineering or a related technical field and 2–4 years of relevant Quality Engineering experience.
  • Solid understanding of IQ, OQ, PQ validation processes and GMP compliance.
  • Ability to work independently and manage multiple tasks effectively.
  • Excellent problem-solving and a proactive approach to challenges.
  • Strong communication and leadership abilities.

Responsibilities

  • Develop and maintain quality evaluation and control systems and protocols.
  • Define inspection, testing and evaluation processes for products and equipment; analyze quality risks.
  • Conduct root cause analysis and implement corrective actions.
  • Provide QA support for both Danvers and Woburn sites and CAPA programs.
  • Collaborate with MRB, CAPA, calibration, validations, and non-conformances across manufacturing and quality operations.

Skills

Independent work
Problem solving
Communication
Leadership

Education

Bachelor's degree in Engineering or related field

Tools

SAP

Job description

Job Function

Supply Chain Engineering

Job Sub Function

Quality Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Danvers, Massachusetts, United States of America, Woburn, Massachusetts, United States of America

Job Description

We are searching for the best talent for a Sr. Quality Engineer, located in Danvers, MA or Woburn, 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

Purpose

In this role, you will have the unique opportunity to contribute to the manufacturing of life-saving medical devices. As part of our "Patients First!" culture, you will play a crucial role in ensuring that high standards of product quality, compliance, and patient safety are maintained.

This individual will be a member of the Quality organization, primarily supporting operations at the Danvers, MA site, with additional support for the Woburn, MA site. The Sr. Quality Engineer will provide Quality Engineering support across manufacturing and quality operations, including areas such as production, incoming inspection, nonconformance management, equipment and calibration, process validation, and other Quality functions as business needs and priorities require.

The successful candidate must be comfortable working across functional boundaries and adapting responsibilities to support changing operational and Quality priorities.

You Will Be Responsible For

Developing, modifying, applying and maintaining quality evaluation and control systems/protocols. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs and analyzes inspection and testing processes, mechanisms and equipment. Conducts quality assurance tests and performs statistical analysis to assess the level of control and manage product quality risks. Undertakes root cause analysis of incidents requiring corrective action.

This individual will need to be able to support both the Danvers and Woburn sites.

  • Document production nonconformity, conduct investigation, assess product risk, recommend disposition in collaboration with other members of MRB.
  • Define and implement action plans and effectiveness monitoring for CAPA originated from Internal/external audits .
  • Coaches team members regarding any Quality Engineering non-conformance, subsequent corrective, and preventive actions, by documenting, investigating, and conducting root cause analysis, and successfully implementing corrective actions.
  • Ensures timely escalation of any Quality Engineering issues or concerns to the next management level.
  • Identifies, under limited supervision, any Quality Engineering non-conformance, subsequent corrective, and preventive actions, by documenting, investigating, and conducting root cause analysis, and successfully implementing corrective actions.
  • Support process validations/revalidation on current and new processes. (IQ, OQ, PQ)
  • Support incoming inspection department as needed.
  • Collaborate with equipment department for PM and calibration procedural updates. Support for non-conformities from failed calibration, etc.
Qualifications/Requirements
  • Bachelor’s degree in Engineering or a related technical field and 2–4 years of relevant Quality Engineering or related experience.
  • Solid understanding of IQ, OQ, PQ validation processes and GMP compliance.
  • Proven track record to work independently and manage multiple tasks effectively.
  • Excellent problem-solving skills and a proactive approach to challenges.
  • Strong communication skills, with the ability to mentor and lead teams effectively.
Preferred
  • Working knowledge of SAP.
  • Preferred certifications: ASQ Certified Quality Engineer (CQE).
  • Knowledge of electrical systems, Schematic drawing and IPC 610 is a plus.
  • Experience in medical device industry working under FDA regulations (21 CFR part 820), ISO 13485 and EU MDR. ISO 13485 Internal audit certificate is a plus.
Other
  • Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
  • This role is eligible for immigration sponsorship, if required. Relocation support is not available for this position.

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.

The anticipated base pay range for this position is :

$79,000.00 - $127,650.00

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)).

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
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