PURPOSE/SUMMARY

Provide Quality Engineering support to ensure compliance with the Quality System, regulatory requirements and the business strategy of the company. Represents Quality as a team member to support new product development, procurement, manufacturing, returns and servicing of products produced.

PRIMARY DUTIES AND RESPONSIBILITIES

• Cross Functional Team member to support new product development, procurement, manufacturing and servicing processes representing Quality Engineering discipline.
• Completes assigned Quality Engineering tasks to schedule.
  • Promotes awareness of Quality and Regulatory requirements.
  • Leads or participates in the development of process and procedure development/changes.
  • Applies statistical process control (SPC) methods to evaluate current processes and process changes.
  • Develops new approaches to solve problems identified as part of the team.
• Assist in the implementation, compliance, and maintenance of standards (e.g., FDA, ISO13485) and any Quality policies and procedures.
• Trains location personnel on all aspects of the Quality System and regulatory standards.
• Applies the requirements of the Quality System to processes, products or services for the location.
  • Supports the manufacturing line to address quality issues and resolution.
  • Provides support to metrology and preventive maintenance programs.
  • Supports validation and verification strategy for new and existing products and processes as assigned.
  • Supports the development and maintenance of Master Validation Plans.
  • Participates in the CAPA process as required as an assignee or project team member.
  • Investigates escalated product complaints to root cause to ensure timely customer response and correction.
  • Monitors product and process performance metrics and acts upon trends (positive or negative).
  • Supports MRB as a team member to ensure proper disposition of non-conformances.
  • Authors, collaborates, and approves Quality System documentation including change orders, DHF, DMR, DHR, labels and labeling, etc.
  • Conducts internal, vendor, and process audits to schedule.
  • Interfaces with suppliers to resolve Quality issues.
• Develops and drives measurable Quality improvements relating to products, processes and services.
• All other essential related duties as required

SUPERVISOR RESPONSIBILITIES

• None

EDUCATION AND/OR EXPERIENCE

• Bachelor’s degree in Engineering discipline or equivalent.
• 0-3 year’s related experience and/or training; preferably in the medical device industry related to process/quality engineering.

ESSENTIAL KNOWLEDGE, SKILLS AND ABILITIES

• Knowledge of basic mechanical testing and material properties.
• Knowledge of metrology.
• Requires background and familiarity with U.S. FDA QSR, requirements including ISO 9001, MDD 93/42, ISO 13485-2003, and Canadian Medical Device requirements.
• ASQ certifications in one or more of the following areas is preferred but not required: Certified Quality Engineer (CQE), or Certified Quality Auditor (CQA).
• Working knowledge of problem solving skills # good statistical and analytical skills.
  • Working knowledge of Problem Solving Tools (i.e. Process Mapping, Histograms, FMEA, Risk Assessment, Cause & Effect Diagrams, PDCA, Pareto Analysis, etc.)
  • Working knowledge of Quality Tools (i.e. Quality Planning, Quality Costs and Assessment, Basic Statistics, Advance Statistical Techniques, Technical Writing, Metrology & Calibration, Inspection and Testing, Sampling Principles and AQL, TQM, Lean, Six Sigma, etc.)
• Good verbal and written communication skills demonstrated by ability to generate technical reports, and ability to make presentations to middle and upper management
• Proven Project Management skills.
• Proficient in the use of Information Technology and applications.

PHYSICAL DEMANDS

• Lift/Carry 25 lbs                                   
• Stand/Sit/Walk 8-10 hrs a day          
• Dexterity required
• Vision requirements correctable to 20/20 vision           

WORK ENVIRONMENT / EXPOSURE

• Climate controlled environment
• Very clean
• Chemicals/Solvents           
• Clean Room        
• Eye Protection
• Safety Shoes
• Laser

Nissha Medical Technologies is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion, creed, gender, gender identity, gender expression, national origin, age, disability, marital or veteran status, sexual orientation or any other legally protected status. In addition, NMT will provide reasonable accommodations for qualified individuals with disabilities.
If you need assistance with completing the online application process, please call 419-660-4122