Manufacturing Engineer puesto vacante

Vacancy caducado!

Primary responsibilities include: Create and update manufacturing process documentation and align with EU MDR requirements. Other responsibilities in support of operational goals include developing manufacturing processes, integration of lean manufacturing and six sigma concepts into the organization, and project planning. Identify and implement process improvements on the production floor.

ESSENTIAL DUTIES AND RESPONSIBILITIES: Primary responsibility is to establish validated manufacturing processes. Monitor vital process inputs and outputs. Basic understanding of light duty medical device manufacturing processes; laser etching, semi-automated assembly equipment, polymer processing technologies, semi-automated packaging processes. Strong understanding of process validation requirements and collaborate with the creation of validation documentation. Familiarity of generating design assurance documentation for machine qualification. Experience in participation of Kaizen events for targeted areas of improvement. Hands-on Individual with detailed trouble shooting capabilities. Ability to train operations personnel for new processes. Teams with manufacturing to document the required manufacturing procedures. Provides engineering support to manufacturing and quality control as necessary. Understanding of a Quality System Requirements and how to work within the Medivators QSR for our products. Basic knowledge and application of Lean Manufacturing and Six Sigma techniques in manufacturing. Basic knowledge and application of injection molding, machining processes and design of tooling/fixturing. Proficient in Microsoft Office Suite Works in a team environment with all levels of the organization. Assist in the review of risk management assessment of processes and procedures.

QUALIFICATIONS REQUIRED FOR POSITION: Education: Must have Bachelor of Science degree in Mechanical, Industrial, Manufacturing Engineering, BioMedical Engineer or equivalent. Minimum of 5-7 years of engineering experience in a medical manufacturing environment. Lean Manufacturing/Lean Six Sigma experience a plus. Must be authorized to work in the United States on a full-time basis for any employer.

Skill/Experience/Education

Mandatory I need people who are self-starters, can work well in a team environment, have experience refining process documentation and perform process characterizations as well as process validations. They need to be doers, not just leaders, they cannot be green or from another industry. Medical Device Experience is a must. They need to be familiar with light duty manufacturing process, and comfortable working in a clean room environment.

At Advantage Resourcing, our primary objective is to perfectly align the best people with the appropriate jobs. These jobs may be temporary assignments or career positions. We place talented people in a wide variety of jobs working with our client companies in areas such as: engineering, IT, technical, manufacturing, skilled trades, distribution, call centers, clerical, accounting, finance and sales.

Our strength is being able to solve our client's workforce needs by matching people that have the right skills, knowledge and motivation to each opportunity. Advantage Resourcing can help you discover the personal and career success you desire.

Advantage Resourcing Americas, Inc. is an Equal Opportunity Employer offering employment without regard for race, color, religious creed, national origin, ancestry, gender, marital status, age, sexual orientation, sex, gender identity, disability, veteran status, or other legally protected categories. Advantage Resourcing is a VEVRAA Federal Contractor.

Vacancy caducado!

ID	#12361914
Estado	Minnesota
Ciudad	Plymouth
Tipo de trabajo	Contract
Salario	USD TBD TBD
Fuente	Advantage Technical Resourcing
Showed	2021-04-18
Fecha	2021-04-17
Fecha tope	2021-06-16
Categoría	Arquitecto/ingeniero/CAD
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Job Details

Manufacturing Engineer