MedTech Senior Project Engineer

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 https://www.jnj.com

Job Function:
Supply Chain Engineering

Job Sub Function:
Project Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom

Job Description:

About Orthopaedics

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 Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.

Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness.

Learn more at https://www.jnj.com/medtech

We are searching for the best talent for MedTech  Senior Project Engineer.

Purpose: As a Senior Project Engineer in the MedTech industry, you will play a key role in leading and handling the engineering aspects of innovative medical device development and manufacturing projects.

You will collaborate closely with multi-functional teams, quality, regulatory, and manufacturing, to ensure timely and successful project delivery while adhering to strict regulatory standards and industry best practices.

This role requires a proven background in engineering principles, excellent project management skills, and a detailed understanding of FDA, BSI, and other regulatory requirements pertinent to medical devices.

You will be responsible for:



* Lead equipment design, validation, and process improvement projects to enhance manufacturing efficiency and compliance.


* Ensure adherence to all compliance, EHS, and safety policies and guidelines.


* Collaborate with vendors to procure equipment, ensuring conformance to regulatory and quality standards.


* Perform and document installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities.


* Create production documentation and contribute to the development of new product BOMs and routings.


* Support regulatory submissions, including technical writing, data analysis, and trend tracking for PMA submissions.


* Develop and manage project budgets, provid...