The Senior Manufacturing Engineer is responsible for overseeing the design, development, and implementation of manufacturing processes and systems and play a critical role in optimizing operational performance, driving continuous improvement, and ensuring the efficient production of high-quality goods.
The Senior Manufacturing Engineer collaborates with cross-functional teams, including product engineers and production staff, to improve processes, enhance efficiency, and maintain rigorous quality standards, lead initiatives to optimize workflows, implement new technologies, and drive innovation within the manufacturing function.
The Senior Manufacturing Engineer also ensures compliance with health and safety regulations and fosters a culture of safety awareness. Overall, their expertise and leadership contribute to the success and profitability of the organization's manufacturing operations.
§ Design and develop innovative manufacturing processes and systems to enhance efficiency and productivity, with the authority to make recommendations and implement approved changes.
§ Collaborate with customers to ensure designs are manufacturable and meet production requirements, providing expertise and guidance in the decision-making process.
§ Work closely with production staff to identify areas for improvement and implement strategies for efficiency enhancement and quality standards, with the authority to lead and coordinate improvement initiatives.
§ Analyze manufacturing processes, workflows, and equipment to identify optimization opportunities and implement changes to improve resource utilization and production outcomes, with the authority to initiate and drive process improvement projects.
§ Collaborate with procurement and supply chain teams to identify cost-saving opportunities without compromising quality or customer satisfaction, with the authority to make recommendations for cost reduction initiatives.
§ Establish and maintain rigorous quality standards throughout the manufacturing process, conducting audits and developing corrective action plans, with the authority to enforce quality control procedures and initiate necessary actions.
§ Lead manufacturing engineering efforts for new product introductions, ensuring seamless transition from product design to production, with the authority to provide input and make decisions regarding manufacturability and scalability.
§ Identify and evaluate the need for new manufacturing equipment or technologies to improve productivity, quality, or capacity, with the authority to research, propose, and justify capital investments.
§ Foster a culture of continuous improvement by leading and participating in lean initiatives, Six Sigma projects, and process improvement efforts, with the authority to facilitate cross-functional teams and drive change.
§ Facilitate cross-functional teams to identify areas for improvement, implement changes, and monitor progress towards goals, with the authority to coordinate and delegate tasks to team members.
§ Bachelor's degree in mechanical engineering, industrial engineering, or a related field.
§ 5+ years of hands-on experience in manufacturing engineering, preferably within the medical industry.
§ Strong understanding of manufacturing principles and practices, including lean manufacturing methodologies.
§ Proven ability to work independently and collaboratively within cross-functional teams.
§ Excellent problem-solving and analytical skills, with a keen attention to detail.
§ Excellent communication and interpersonal skills, with the ability to effectively convey complex concepts to diverse audiences.
§ Advanced knowledge of manufacturing software and tools, such as CAD/CAM, simulation software, and statistical analysis tools.
§ Strong project management skills, with the ability to plan, execute, and deliver projects on time and within budget.
§ Experience in implementing and driving continuous improvement methodologies, such as Lean Six Sigma, Kaizen, or 5S.
§ Familiarity with regulatory requirements and industry standards related to manufacturing processes, such as ISO 13485 and FDA regulations.
§ Proven ability to collaborate effectively with cross-functional teams, including product development, quality assurance, and supply chain.
§ Experience in leading and mentoring junior engineers, providing guidance and support for their professional development.
§ Excellent data analysis skills, with the ability to gather, interpret, and present complex data in a clear and concise manner.
§ Strong problem-solving aptitude, with the ability to identify root causes, develop innovative solutions, and implement preventive measures.
§ Demonstrated ability to adapt to changing priorities, manage multiple projects simultaneously, and thrive in a fast-paced, deadline-driven environment.
§ Professional certifications in manufacturing engineering such as Six Sigma Green/Black Belt, are desirable but not mandatory.
§ English 90% (spoken and written).
Tipo de puesto: Tiempo completo
Sueldo: $1,800.00 - $2,300.00 al día
Horario:
Lunes a viernes
Turno de 10 horas
Turno matutino
Prestaciones:
Estacionamiento de la empresa
Opción a contrato indefinido
Seguro de gastos médicos mayores
Vacaciones adicionales o permisos con goce de sueldo
Vales de despensa
Puede trasladarse/mudarse:
22740, Rosarito, B.C.: Trasladarse al trabajo sin problemas o planear mudarse antes de comenzar a trabajar (Obligatorio)
Experiencia:
IQ, OQ Y PQ: 5años (Obligatorio)
Diseño de experimentos: 3años (Obligatorio)
Administracion de proyectos: 3años (Obligatorio)
ISO 13485: 3años (Obligatorio)
Industria Medica: 3años (Deseable)
Idioma:
Inglés (Obligatorio)
Lugar de trabajo: Empleo presencial
Fecha de inicio prevista: 01/07/2024
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