# Device Life Cycle Engineer at Johnson & Johnson

Johnson & Johnson is hiring a Device Life Cycle Engineer in Antwerp, Belgium. It pays €73k-€115k a year and Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/74b913eb-3a17-488d-9554-b6a202ff5f4b?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Beerse, Antwerp, Belgium.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Beerse, Antwerp, Belgium
- Salary: €73k-€115k
- Posted: October 30, 2026
- Apply: https://jobsbylevel.com/go/74b913eb-3a17-488d-9554-b6a202ff5f4b?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=device-life-cycle-engineer-at-johnson-johnson-9428c2

## Prepare for this job

The job page lists 4 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/device-life-cycle-engineer-at-johnson-johnson-9428c2

## 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. Job Function: Supply Chain Engineering Job Sub Function: Process Engineering Job Category: Scientific/Technology All Job Posting Locations: Beerse, Antwerp, Belgium, Schaffhausen, Switzerland Job Description: Senior Device & Packaging Lifecycle Engineer The Senior Device Lifecycle Engineer supports the Device & Packaging Value Optimization Team as part of Drug Product MSAT Organization. This position is based at the Schaffhausen, Switzerland or Beerse Manufacturing location in Belgium. MSAT is a supply chain division of the f Johnson & Johnson Innovative Medicines (J&J). MSAT is a worldwide organization, working in close partnership with Manufacturing Technical Operations (MTO) and PCD Primary Container and Device Development (R&D) organizations. The primary focus of MSAT is to provide technical competence and manufacturing science & technologies to J&J’s pharmaceutical environment and product portfolio. The senior device lifecycle engineer is responsible for the ongoing lifecycle engineering and technical support for combination products in the J&J Supply Chain network. The senior engineer transitions the responsibilities from development to manufacturing and takes accountability for technical support including design change control, process improvements, tech transfers, complaint analysis, CAPA and audit support as required. The senior device lifecycle engineer is the technical key point of contact to site operations and quality leadership for his area of responsibility. The senior device lifecycle engineer ensures that all validation activities and ongoing production conducted at suppliers, external manufacturers and internal manufacturing and assembly facilities are in compliance with all applicable procedures and to the requirements of 21 CFR Parts 3, 4,11, 210, 211 and 820 and Johnson & Johnson Policy Standards related to Good Manufacturing Practice (cGMP) for Combination Products, Pharmaceuticals, and Medical Devices. The Senior Device Lifecycle Engineer leads and manages product and process quality improvement and reliability projects to stabilize new manufacturing processes as necessary using quality engineering and process excellence (six-sigma) tools. The Senior Device Lifecycle Engineer participates in a cross-functional team executing design changes, network and production capacity changes for growing and established combination products. PRINCIPAL RESPONSIBILITIES: Device manufacturing process capacity scale-up for internal and external manufacturing, all technical aspects of capacity scale-up to support global demand for the product life-cycle Develop and qualify additional supplier capacity (multi-cavitation for plastic molded components, other process technologies as necessary) per quality systems requirements, Develop and qualify additional capacity for sub-assembly and assembly processes per manufacturing network strategies. Device life-cycle engineering including process engineering, product engineering and support to site or external manufacturing network as necessary. Viewed as a subject matter expert in one or more aspects of the end to end medical device development and supply chain. Support

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