Manufacturing Engineer II
Spectraforce
US
21 hours ago
Job Description
Cartago on-site, 12 month contract
Key Responsibilities:
• Optimize manufacturing processes, including using engineering methods (e.g., SIX Sigma and LEAN methods) for continuous process improvement and/or re-design/design of equipment, tools, fixtures, etc. to improve manufacturing processes, employing technical design skills
• Develop moderately complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
• Analyze and resolve moderately complex Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
• Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
• Establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
• Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
•Execute the complete process to ensure fixture and tool readiness for the manufacturing process, from purchasing through final validation
•Carry out a variety of tasks across multiple systems to ensure seamless operations and support business processes
• Other incidental duties assigned by Leadership
Required Experience:
Bachelor's Degree or equivalent in Engineering or Scientific field Required
2-3 years of experience as a manufacturing engineer, managing the complete life cycle of projects, experience in transfer projects, inventory management, approval of SOPs documentation, experience in process and product validation.
Advanced English level B2+ 85%
Good computer skills in usage of MS Office Suite including MS Project; CAD experience preferred (if applicable)
Previous experience working with lab/industrial equipment preferred (if applicable)
Basic understanding of statistical techniques
Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
Good problem-solving, organizational, analytical and critical thinking skills
Good understanding of processes and equipment used in assigned work
Basic documentation, communication and interpersonal relationship skills
Knowledge of Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
Strict attention to detail
Ability to interact professionally with all organizational levels
Ability to manage competing priorities in a fast-paced environment
Must be able to work in a team environment; and may interact with vendors
Ability to build stable working relationships internally
Key Responsibilities:
• Optimize manufacturing processes, including using engineering methods (e.g., SIX Sigma and LEAN methods) for continuous process improvement and/or re-design/design of equipment, tools, fixtures, etc. to improve manufacturing processes, employing technical design skills
• Develop moderately complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
• Analyze and resolve moderately complex Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
• Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
• Establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
• Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
•Execute the complete process to ensure fixture and tool readiness for the manufacturing process, from purchasing through final validation
•Carry out a variety of tasks across multiple systems to ensure seamless operations and support business processes
• Other incidental duties assigned by Leadership
Required Experience:
Bachelor's Degree or equivalent in Engineering or Scientific field Required
2-3 years of experience as a manufacturing engineer, managing the complete life cycle of projects, experience in transfer projects, inventory management, approval of SOPs documentation, experience in process and product validation.
Advanced English level B2+ 85%
Good computer skills in usage of MS Office Suite including MS Project; CAD experience preferred (if applicable)
Previous experience working with lab/industrial equipment preferred (if applicable)
Basic understanding of statistical techniques
Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
Good problem-solving, organizational, analytical and critical thinking skills
Good understanding of processes and equipment used in assigned work
Basic documentation, communication and interpersonal relationship skills
Knowledge of Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
Strict attention to detail
Ability to interact professionally with all organizational levels
Ability to manage competing priorities in a fast-paced environment
Must be able to work in a team environment; and may interact with vendors
Ability to build stable working relationships internally