The Manufacturing Engineer II applies knowledge of technical principles and Edwards systems and procedures to optimize manufacturing processes.

Job Functions:

Improve manufacturing processes using engineering methods (e.g.,  LEAN methods, basic statistics) for continuous process improvementDevelop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyse results, make recommendations, and develop reportsAnalyse and resolve basic 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 processesEstablish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processesOversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work

Required Education & Skills:

A Bachelor’s degree in Mechanical, Biomedical, or equivalent engineering degree is required.Minimum of 2 years’ experience in Engineering or Scientific field including either industry or industry/educationGood computer skills in usage of MS Office Suite including MS Project; CAD experience preferred (if applicable)Basic documentation, communication (e.g., written and verbal) and interpersonal relationship skillsBasic understanding of statistical techniquesPrevious experience working with lab/industrial equipment preferred (if applicable)Good understanding and knowledge of principles, theories, and concepts relevant to EngineeringGood problem-solving, organizational, analytical and critical thinking skillsGood understanding of processes and equipment used in assigned workKnowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturingStrict attention to detailAbility to interact professionally with all organizational levelsAbility to manage competing priorities in a fast paced environmentMust be able to work in a team environment, including immediate supervisor and other team members in the section or group; and may interact with vendorsAbility to build stable working relationships internallyAdhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control