Device Life Cycle Engineer
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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 .
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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 proc...
- Rate: Not Specified
- Location: Beerse, BE-VAN
- Type: Permanent
- Industry: Finance
- Recruiter: Johnson and Johnson
- Contact: Not Specified
- Email: to view click here
- Reference: R-107597
- Posted: 2026-11-03 07:31:52 -
- View all Jobs from Johnson and Johnson
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