Senior Validation Engineer
Job in
Danvers, Essex County, Massachusetts, 01923, USA
Listed on 2026-06-11
Listing for:
Johnson & Johnson
Full Time
position Listed on 2026-06-11
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer, Process Engineer, Biomedical Engineer
Job Description & How to Apply Below
more at
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:
Manufacturing 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 Sr. Validation Engineer.
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.
Responsibilities:
* Take charge of the validation efforts for new manufacturing processes, guaranteeing consistency to regulatory standards and widely accepted guidelines in the industry.
* Develop and implement process validation protocols and reports, carefully documenting findings and ensuring successful implementation.
* Collaborate with multi-functional teams to establish validation requirements and timelines.
* Conduct risk assessments and implement mitigation strategies to ensure the successful implementation of validated processes.
* Continuously improve and optimize existing manufacturing processes to drive efficiency and quality.
* Offer technical expertise and mentorship to colleagues within the company, ensuring compliance with validation protocols and procedures.
* Stay up-to-date with industry trends and regulatory changes to proactively identify areas for improvement.
Requirements:
* Bachelor's degree in Engineering or related field. Master's degree preferred
* Minimum of 7 years of experience in process validation (including TMV, CSV) within a manufacturing environment.
* Proven track record of successfully conducting process validation strategies and protocols.
* Strong knowledge of regulatory requirements and industry standards related to process validation.
* Exceptional problem-solving skills and attention to detail.
* Excellent communication and teamwork skills, with the ability to work effectively in multi-functional teams.
* Strong motivation to succeed and a dedication to achieving high standards.
* Fluency in written and spoken English.
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, please contact us via or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is: $94,000 - $151,800.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position…
Position Requirements
10+ Years
work experience
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