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Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us change equals opportunity. Every day our colleagues are challenging whats possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
SUMMARY DESCRIPTION
The Manufacturing Engineer II supports Operations goals and objectives especially as related to quality improvements cost reductions cycle reductions and product delivery. Works closely with purchasing to ensure suppliers are qualified have validated processes and assure components are compliant to specifications. Maximizes efficiency by analyzing layout of equipment workflow assembly methods and work force utilization standards in order to achieve manufacturing goals according to product specification and cost reduction initiatives. Assures compliance with approved methods and quality standards.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.
Troubleshoot and analyze effectiveness of processes. Implement actions to improve equipment uptime yield efficiencies and quality of production.
Apply standard manufacturing analysis techniques such as flowcharting Pareto analysis cause & effect diagrams root cause and statistical process control to reduce variation and improve quality of manufactured as well as purchased components.
Lead the Lifecycle Management projects for the Cincinnati site to maintain and improve Integras existing core products.
Establish manage and communicate priorities for Lifecycle Management projects to Integras Leadership Team.
Organize and lead process reviews with production and engineering personnel prepare clear process procedures/instructions to be used and understood by shop personnel.
Champion the process towards rework s and labor variance reduction/elimination.
Lead the Engineering activities in a collaborative crossfunctional team environment.
Create update and maintain routers rework routers DMR and any other Operations technical documents including DHF.
Provide other technical guidance and/or assistance as required by the business.
DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge skill and/or ability required for this position.
Education & Experince:
Bachelors degree in a technical discipline with 3 years of experience in a manufacturing environment or a Masters degree with 02 years of experience or equivalent education and years of experience
Medical device experience is preferred.
Working knowledge of manufacturing basic machine and tool design and start up & trouble shooting of new equipment and processes.
Experience in implementing TQM SPC Continuous Improvement Cellular Flow JIT 5S and Cycle Time Reduction is desirable.
Six Sigma black or green belt certification preferred.
Previous supervisory experience and/or experience working with production associates is preferred.
Strong interpersonal & communication skills; ability to coach train and lead others.
Experience with statistical software.
Demonstrated cost reduction and quality improvement results.
Proficiency with development tools (e.g. Solidworks AutoCad).
Proficient in Microsoft Project.
Integra LifeSciences is an equal opportunity employer and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race marital status color religion sex age national origin sexual orientation physical or mental disability or protected veteran status.
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Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation please email us at or call us at.
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Full-Time