Senior Manufacturing Engineer

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🎰 Nevada – Remote

🎰 Nevada – Remote

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🟠 Senior

👷🏻‍♀️ Ingenieur

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ZEISS Group

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10.000+ Mitarbeiter

🏭 Fertigung

🏥 Gesundheitswesen

🧬 Biotechnologie

Manufacturing • Healthcare • Biotechnology

ZEISS ist ein international führendes Technologieunternehmen, das in den Bereichen Optik und Optoelektronik tätig ist. Im vergangenen Geschäftsjahr erzielte die ZEISS Gruppe einen Jahresumsatz von insgesamt 10 Milliarden Euro in ihren vier Segmenten Halbleitertechnik, Industrielle Messtechnik & Forschung, Medizintechnik und Verbrauchermärkte (Stand: 30. September 2023). Mit rund 43.000 Mitarbeitern ist ZEISS weltweit in fast 50 Ländern aktiv und verfügt über rund 30 Produktionsstandorte, 60 Vertriebs- und Servicegesellschaften sowie 27 Forschungs- und Entwicklungszentren (Stand: 30. September 2023). Das 1846 in Jena gegründete Unternehmen hat seinen Hauptsitz in Oberkochen, Deutschland. Die Carl Zeiss Stiftung, eine der größten Stiftungen in Deutschland, die der Förderung der Wissenschaft gewidmet ist, ist alleinige Eigentümerin der Holdinggesellschaft Carl Zeiss AG. Datenschutz: www.zeiss.com/data-protection Impressum: http://zeiss.com/publisher Dies ist der offizielle LinkedIn-Account von ZEISS. Er folgt der ZEISS Netiquette: www.zeiss.com/netiquette

Beschreibung

• Strategically manage and prioritize multiple concurrent projects and objectives, ensuring optimal allocation of resources and alignment with organizational goals. • Lead and facilitate design reviews, providing expert guidance across cross-functional teams (R&D, QA, OPS) to drive innovation and ensure compliance with regulatory standards. • Identify, champion, and implement process and procedural improvements to enhance manufacturing efficiency, product quality, and regulatory compliance. • Promote and embed lean manufacturing principles throughout the organization, driving continuous improvement and operational excellence. • Oversee the creation and maintenance of comprehensive product documentation, including component specifications, BOMs, CAD models and drawings, manufacturing instructions, and lot history records. • Direct the development, maintenance, and improvement of manufacturing equipment, tooling, and fixturing, ensuring reliability and scalability. • Author, execute, and supervise test protocols, analyze test data, and prepare detailed test reports to support validation and verification activities. • Lead process validation and equipment qualification efforts, ensuring all manufacturing processes meet regulatory and quality requirements. • Develop and maintain detailed project schedules, ensuring timely completion of milestones and deliverables. • Monitor manufacturing production yield and throughput; proactively identify issues and implement solutions to improve performance and minimize disruptions. • Establish, monitor, and evaluate key performance indicators for manufacturing processes, driving data-driven decision-making and continuous improvement. • Provide leadership and guidance to the assembly team, fostering a culture of quality, consistent manufacturing output, and high yields. • Travel periodically as required to support project deliverables, supplier audits, and organizational needs. • Initiate and oversee Document Change Orders and Nonconformance Material Reports activity; actively participate in Corrective and Preventive Actions as required.

🎯 Anforderungen

• Bachelor's or Master’s degree in Mechanical Engineering preferred; certifications in leadership or medical device design are highly valued. • At least 7 years of engineering experience, ideally in regulated industries, with proven leadership in cross-functional teams and projects. • Strong interpersonal and collaborative skills; ability to mentor teams and communicate effectively; expert problem solver. • Skilled in SolidWorks CAD for complex fixture and tooling design, overseeing reviews and implementation across projects. • Deep knowledge of materials and processing methods; adept at optimizing for performance, manufacturability, and compliance. • Advanced training in GMP and ISO 13485; experienced in maintaining quality systems and driving improvement. • Lean Six Sigma expert with a history of leading successful process improvements and team training. • Proactive in identifying and solving technical and operational challenges, ensuring effective corrective actions across departments. • Significant clean room (CER) operations experience, including staff training and compliance leadership. • Able to perform basic movements and tasks; comfortable with exposure to manufacturing materials.

🏖️ Vorteile

• Medical • Vision • Dental • 401k Matching • Employee Assistance Programs • Paid time off