Senior Engineer

Radiant Systems Inc; Draper (UT); On-site; USD 70,000 - 100,000; Full time

Job summary

Radiant Systems Inc in Utah is seeking a Quality Engineer to lead manufacturing process improvements using Six Sigma and Lean methods. You will identify redesign opportunities for equipment, monitor critical control points, and drive development of robust test methods and process validations.

The ideal candidate holds a Bachelor's in engineering/science with 2+ years of industry experience, or a Master's with 1+ year, and is ASQ CQE certified or working toward it.

Qualifications

• Bachelor's degree in related engineering/science with 2+ years industry experience.
• Master's degree in related field with 1+ year industry experience.
• ASQ CQE certification preferred.
• Six Sigma Green Belt or higher preferred.

Responsibilities

• Lead development and optimization of manufacturing processes using Six Sigma and Lean methods.
• Identify opportunities to redesign equipment, tools, and fixtures to reduce risk.
• Monitor Critical Control Points.
• Lead experiments and validate processes; write protocols and analyze results.
• Collaborate with engineers on equipment selection and validation.
• Develop training materials and documentation for production and Receiving Inspection.
• Lead investigations of quality issues (NCR, CAPA, SCAR) and document findings.
• Oversee change control and ensure compliance.

Skills

MS Office Suite

Read drawings

Documentation & communication

Interpersonal skills

CQE knowledge

Six Sigma

Quality engineering

Problem solving

Process knowledge

Leadership

EH&S compliance

Attention to detail

Teamwork

Automation experience

Software testing & validation

Education

Bachelor's degree in Materials Science/Mechanical/Chemistry

Master's degree in Materials Science/Mechanical/Chemistry

Job description

• Lead identification, development, and optimization of Manufacturing processes using engineering methods (e.g., Six Sigma and Lean manufacturing tools) for continuous process improvement initiatives.
• Identify opportunities & implement solutions for re‑design/design of equipment, tools, fixtures, etc. to improve manufacturing processes and reduce overall process/product risk profile.
• Monitor Critical Control Points.
• Drive the development and manage the execution of experiments and tests (including writing and executing protocols) to improve products (including evaluation of source materials and suppliers) and establish robust manufacturing processes/test methods based on engineering principles; ensure completion of process validations (TMV/IQ/OQ/PQ), including analyzing results and developing reports; collaborate with cross-functional team members to facilitate project success and on-time completion.
• Collaborate with engineers for equipment selection and validation.
• Develop training and documentation materials for production and Receiving Inspection(e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes.
• Develop and sustain technical content of risk management files.
• Lead in the investigation of complex manufacturing product quality and compliance issues (e.g., Material Review Board, NCR, SCAR, CAPA, non-conformances, audit observations) for all production processes and based on engineering principles; analyze results, make recommendations and develop reports.
• Oversee Quality support tasks; gives instruction to engineers/technicians on conducting tests; trains engineers/ technicians and operators and provides feedback; and may coordinate engineers/ technician work.
• Lead, review and approve compliant change control.

Education/Experience Requirements

• Bachelor's Degree in related Engineering/Science field (Materials Science, Mechanical Engineering, Chemistry) with 2+ years industry experience
• Master's Degree in related Engineering/Science field (Materials Science, Mechanical Engineering, Chemistry) with 1+ years industry experience

Preferred

• ASQ Certified Quality Engineer (CQE)
• Six Sigma Green Belt or better

Required Skills

• Proven expertise in usage of MS Office Suite
• Ability to read and interpret drawings
• Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills
• Ability to translate technical information to all levels of the organizations
• Extensive knowledge and understanding and knowledge of principles, theories, and concepts relevant to Quality Engineering (e.g., CQE body of knowledge)
• Knowledge of Six Sigma concepts with ability to apply to work product
• Knowledge of Quality Engineering concepts with ability to apply to work product
• Problem-solving, organizational, analytical and critical thinking skills
• Understanding of processes and equipment used in assigned work
• Strong leadership skills and ability to influence change
• Knowledge of and adherence to Client Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast-paced environment
• Work is performed independently
• Must be able to work in a team environment, including frequent inter‑organizational and outside customer contacts
• Experience with automation, software testing, and software validation is strongly preferred