1 день назад
Process Engineer (MedTech)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Process Engineer (MedTech) (Manufacturing, GMP/ISO/FDA): Planning and executing engineering, validation, and change control projects within a regulated medical device manufacturing environment with an accent on process improvement, equipment qualification, and technical compliance. Focus on designing experiments, solving production and quality issues through root cause analysis, and implementing robust solutions across cross-functional operations.
Location: Jacksonville, Florida, United States of America; onsite
Company
Johnson & Johnson MedTech develops healthcare and vision care products and services, combining medical science, technology, and manufacturing expertise.
What you will do
- Plan and execute moderately complex engineering, change control, and manufacturing improvement projects.
- Translate technical requirements into manufacturing, product, equipment, or process specifications.
- Plan and execute equipment, system, process, packaging, and materials qualification activities, including vendor and site acceptance testing.
- Lead or support validation activities, including IQ/OQ/PQ protocol execution and reporting.
- Improve efficiency, yield, reliability, safety, and process performance through experiments, statistical analysis, and continuous improvement.
- Investigate deviations, nonconformances, downtime, rejects, and CAPAs using structured problem-solving and root cause analysis.
Requirements
- Bachelor’s degree in Engineering or a related technical discipline.
- 2–4 years of relevant engineering experience in manufacturing or regulated industry environments.
- Demonstrated experience executing engineering or technical projects.
- Strong analytical, problem-solving, communication, collaboration, organizational, and technical writing skills.
- Working knowledge of project management fundamentals and common office and data analysis tools.
- Ability to work in a regulated environment with GMP, ISO, FDA, GDP, and company quality requirements.
Nice to have
- Experience in ISO- or FDA-regulated environments.
- Experience with qualification, validation, and change control activities.
- Exposure to Lean, Six Sigma, Gemba Kaizen, or structured problem-solving methodologies.
Culture & Benefits
- Inclusive work environment focused on individual dignity, diversity, and equal opportunity.
- Cross-functional collaboration with Operations, Quality, Engineering, Supply Chain, and external vendors.
- Limited domestic and/or international travel may be required based on business needs.
- Reasonable accommodation is available throughout the interview process for applicants with disabilities.
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