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Senior Manufacturing Engineer
Location
Nevada
Posted
4 days ago
Salary
0
Seniority
Senior
Job Description
Senior Manufacturing Engineer
ZEISS Group
• 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.
Job Requirements
- 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.
Benefits
- Medical
- Vision
- Dental
- 401k Matching
- Employee Assistance Programs
- Paid time off
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