Reference: Posted: Location: Plymouth, MNCompany: Planet Pharma GroupContact: ApplicationsEmail: may include the following and other duties may be assigned:
· Designs manufacturing processes, procedures and production layouts for the assembly of combination products that support cardiovascular therapies.
· Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; and optimizing device production relative to cost constraints.
· Identifies and implements improvements to reduce production scrap.
· Investigates and dispositions nonconforming product.
· Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
· Develops and maintains manufacturing processes through the use of statistical process control.
· Provides guidance regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
· Designs sequence of operations and specifies procedures for product manufacture.
· Ensures processes and procedures are in compliance with regulations.Must Have:* Bachelor’s degree in engineering (Mechanical, Biomedical, Chemical, or Industrial preferred), and minimum of 2 years of relevant experience, or advanced degree with 0 years of experienceNice to Have:* Operations/Manufacturing experience with desire to improve existing processes.* Experience with problem solving methodologies (e.g. DMAIC) and ability to lead problem solving team.* Effective communication skills (written and verbal) with experience reporting out to leadership.* Experience with statistical software (JMP, Minitab).
· Designs manufacturing processes, procedures and production layouts for the assembly of combination products that support cardiovascular therapies.
· Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; and optimizing device production relative to cost constraints.
· Identifies and implements improvements to reduce production scrap.
· Investigates and dispositions nonconforming product.
· Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
· Develops and maintains manufacturing processes through the use of statistical process control.
· Provides guidance regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
· Designs sequence of operations and specifies procedures for product manufacture.
· Ensures processes and procedures are in compliance with regulations.Must Have:* Bachelor’s degree in engineering (Mechanical, Biomedical, Chemical, or Industrial preferred), and minimum of 2 years of relevant experience, or advanced degree with 0 years of experienceNice to Have:* Operations/Manufacturing experience with desire to improve existing processes.* Experience with problem solving methodologies (e.g. DMAIC) and ability to lead problem solving team.* Effective communication skills (written and verbal) with experience reporting out to leadership.* Experience with statistical software (JMP, Minitab).
MDR – Product Engineer II – Exempt in minneapolis at Unknown Company
This position is listed as full time and onsite.