Senior Manufacturing Engineer

Das ist der Job

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Darum lohnt es sich

The role focuses on improving operational efficiency, reducing scrap, and ensuring product quality through data analysis, Lean Manufacturing, Six Sigma methodologies, and statistical tools. /h3 h3This position acts as a Subject Matter Expert (SME) for manufacturing processes, providing technical support to production and cross-functional teams while supporting process validation, equipment qualification, troubleshooting, new product introductions, and regulatory compliance in accordance with GMP, GDP, and ISO 13485 requirements. /h3 h3bYOUR RESPONSIBILITIES /b /h3 ul liLead continuous improvement initiatives focused on productivity, quality, cost reduction, and operational efficiency within a medical device manufacturing environment. /li liAnalyze manufacturing data to identify trends and root causes, and perform process optimization for scrap reduction and efficiency improvement using Lean Manufacturing, Six Sigma methodologies, statistical analysis, and process capability studies. /li liAct as Subject Matter Expert (SME) for assigned manufacturing processes, optimizing manufacturing operations to ensure product quality, process consistency, and operational efficiency. /li liDevelop and execute process validation activities including IQ/OQ/PQ protocols and validation documentation. /li liProvide day‑to‑day manufacturing and business support to production operations and cross‑functional teams, including troubleshooting and implementation of corrective actions for manufacturing and process‑related issues. /li liCollaborate with production, quality, maintenance, and engineering teams to improve manufacturing performance and process reliability. /li liSupport new product introductions, process transfers, equipment qualifications, risk assessments, and FMEA activities, while also supporting internal and external audits and ensuring compliance with regulatory and quality standards. /li liEnsure manufacturing processes comply with GMP (Good Manufacturing Practice) and GDP (Good Documentation Practice) requirements. /li /ul h3bYOUR BACKGROUND /b /h3 ul liBachelor’s or Master’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related technical field. /li liMinimum 5+ years of experience in medical device manufacturing or other highly regulated industries. /li liLean Six Sigma Green Belt certification desired. /li liStrong experience in manufacturing engineering, process optimization, and validation methodologies. /li liHands‑on experience with process validation, equipment qualification, and manufacturing process controls. /li liStrong understanding of GMP, GDP, ISO 13485, and regulated manufacturing environments. /li liKnowledge of statistical analysis tools and structured problem‑solving methodologies. /li liExcellent analytical, communication, and project management skills. /li liExperience with ERP/MES systems and manufacturing data reporting tools is an advantage. /li liPower BI skills and experience with data visualization/reporting tools are a plus. /li /ul pbYOU ARE REPORTING TO /b /p pProcess Engineering Supervisor II /p h3bOUR OFFER /b /h3 ul liA responsible and varied job in a global company with a strong local presence /li liProgressive employment conditions with long‑term perspective /li liA high level of personal responsibility and independent workA safe space for creative thinking and learning at the workplace /li liBonus system, extra vacation days and many other benefits /li /ul pJabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law. /p h3bAccessibility Accommodation /b /h3 pIf you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. ppAt Jabil (NYSE: JBL), we are proud to be a trusted partner for the world’s top brands, offering comprehensive engineering, supply chain, and manufacturing solutions.

With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions.

Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. /p h3The Senior Process Engineer is responsible for process validation, manufacturing support, and process optimization within a regulated medical device manufacturing environment.

You can request a reasonable accommodation by sending an e‑mail to with the nature of your request and contact information. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to. /p /p #J-18808-Ljbffr