SR MANUFACTURING ENGINEER
Job Overview
What your background should look like:
RESPONSABILITIES
- Transfers R&D projects to manufacturing by completing design drawings, specifications, risk assessments, gauge analyses, qualifications, and validations.
- Lead a dedicated group of engineers and technicians within the Project or Manufacturing Group.
- Ensure engineers are fully integrated within the overall project and production support team.
- Plan and implement training and development plans with subordinates.
- Complete design and development projects by training and mentoring technicians.
- Coach and mentor team members.
- Establish engineering goals and objectives that deliver to results in accordance with the business plan. Identify and establish permanent and effective technical / systems solutions to problems.
- Consistently meet customer requirements and commitment to performance excellence and meet deadlines.
- Prepare product and process reports by gathering, analyzing and summarizing information and trends.
- Champion compliance with Te connectivity medical systems and processes.
- Identify and develop improvements to increase key process metrics of Service, Delivery, Quality and Cost using Lean/6 sigma methodologies.
- Investigate leading edge process technologies and evaluate potential competitive advantage and cost benefit of introduction.
- Lead or guide projects in conjunction with other resource management (i.e. NPI, quality engineering, design assurance, R&D and other cross-functional departments) related to engineering. Work with the team to plan, coordinate and implement activities to support the successful launch of new products, including purchase / buy analysis, introduction of new processes and others. Develop / modify manufacturing processes by studying product requirements; research, design, modify and test manufacturing methods and equipment.
- Maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies.
- Manage external relationships with key technology suppliers.
- Manage a variable workload to meet operational requirements.
- Ensure all health, safety and environmental requirements are met.
- Oversee and drive validation activities including equipment IQ / OQ, process OQ / PQ, process characterization, attribute / variable test method validation and associated documentation.
- In-depth knowledge related to linkages between Validation Master Plan, pFMEA, dFMEA, risk management.
- Define, establish and lead all documentation required to manage manufacturing processes including analytical models, procedures, work instructions, employee training tools, process FMEAs and others.
ABILITIES:
- Ability to Work under pressure.
- Ease of adapting to change.
- Teamwork.
- Commitment to quality and efficiency.
- Seeking continuous improvement.
- Willing to undertake an overseas assignment of up to 3 months and work on own initiative during the assignment.
- Must be fluent in English, both written and verbal, more than 80%.
EXPERIENCE:
- 5-7 years of working experience as a Manufacturing or Process Engineering position.
- Medical device industry experience preferred.
- MS Office Proficiency.
- Experienced user of CAD tools, SOLIDWORKS experience preferred.
- Statistical knowledge including data analysis and use of statistical software (JMP, Minitab, etc.).
- Working knowledge of sigma and/or lean engineering principles with a proven track.
EDUCATION:
- Bachelor's degree in mechanical/process engineering
Competencies
San Rafael - Flexipark, A, CR, 20108
Job Segment:
Manufacturing Engineer, Lean Six Sigma, R&D Engineer, Senior Quality Engineer, Medical Device Engineer, Engineering, Management