Senior Manufacturing Engineer

🕒 il y a 1 mois

🎰 Nevada – Distant

🎰 Nevada – Remote

⏰ Temps Plein

🟠 Senior

👷🏻‍♀️ Ingénieur

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ZEISS Group

Site WebLinkedInTous les Emplois

10 000+ employés

🏭 Fabrication

🏥 Santé

🧬 Biotechnologie

Manufacturing • Healthcare • Biotechnology

ZEISS est une entreprise technologique de premier plan à l'international dans les domaines de l'optique et de l'optoélectronique. Au cours de l'exercice précédent, le groupe ZEISS a généré un chiffre d'affaires annuel totalisant 10 milliards d'euros dans ses quatre segments : Technologie de Fabrication de Semi-conducteurs, Qualité Industrielle & Recherche, Technologie Médicale et Marchés Grand Public (statut : 30 septembre 2023). Avec environ 43 000 employés, ZEISS est actif à l'échelle mondiale dans près de 50 pays, possédant environ 30 sites de production, 60 entreprises de vente et de service et 27 centres de recherche et développement (statut : 30 septembre 2023). Fondée en 1846 à Iéna, l'entreprise a son siège social à Oberkochen, en Allemagne. La Fondation Carl Zeiss, l'une des plus grandes fondations en Allemagne dédiée à la promotion de la science, est l'unique propriétaire de la société holding, Carl Zeiss AG.Protection des données : www.zeiss.com/data-protectionMentions légales : http://zeiss.com/publisher Ceci est le compte LinkedIn officiel de ZEISS. Il suit la Netiquette de ZEISS : www.zeiss.com/netiquette

Description

• 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.

🎯 Exigences

• 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.

🏖️ Avantages

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