Get roles like this, scored and matched, in your inbox.
Sign up free →Job Opening
Manufacturing Engineer
Johnson & Johnson · Uppsala, Uppsala · Posted 3 days ago
Help replace end-of-life manufacturing equipment at J&J's Uppsala site and own process, equipment, and supplier improvements for regulated medical device production.
Job Function: Supply Chain Engineering
Job Sub Function: Manufacturing Engineering
Job Category: Scientific/Technology
All Job Posting Locations: Uppsala, Sweden
Job Description: Manufacturing Engineer J&J Vision Uppsala We are looking for a driven Manufacturing Engineer to lead process, equipment, and supplier-related improvement initiatives, ensuring robust, compliant, and efficient operations that support product quality and business growth. As Manufacturing Engineer, you will play a key role in maintaining, improving, and validating manufacturing processes and equipment. The role also includes working directly with suppliers on the tooling, equipment, and processes used to manufacture supplied materials and components. The Uppsala site is currently replacing end-of-life equipment with new equipment and, for the right person, this is a unique opportunity to contribute and grow with us on this exciting journey! Key Responsibilities:
- Serve as technical owner for assigned process areas and/or supplier-site tooling and equipment used to manufacture supplied materials and components, managing lifecycle activities such as upgrades, maintenance requirements, and obsolescence mitigation.
- Develop, maintain, and coordinate technical review of material and component specifications, translating product and manufacturing requirements into clear supplier requirements in collaboration with R&D and Quality.
- Work directly with suppliers to resolve material and component manufacturing issues, and assess proposed changes at the supplier against internal component specifications and quality requirements.
- Lead root cause investigations using structured problem-solving methodologies (5 Whys, Fishbone, 5M, etc) in alignment with J&J Non-conformity and CAPA processes.
- Plan and implement equipment and process validation activities in accordance with GMP, ISO 13485, and FDA 21 CFR Part 820 requirements, including Computerized System Validation where applicable.
- Collaborate cross-functionally with R&D, Quality, and Supply Chain to support technology transfer and automation initiatives and to ensure Design for Manufacturability and Assembly (DFMA).
- Foster a culture of innovation, safety, and continuous improvement across the manufacturing organization.
…
This posting is sourced from Johnson & Johnson's own career site — applying takes you there directly.
Get roles like this, scored and matched, in your inbox.
Sign up free →Related roles
This role centers on Gmp, Iso 13485, Fda 21 Cfr Part 820, and Change Control. There are 1,974 open roles at Johnson & Johnson right now.
Want roles like this found for you?
Set your Focus once. Career Engine screens every new opening every week.
A scored, explained shortlist — not a keyword match — delivered weekly. Free for one profile.