Quality Engineer

Belcan Corporation; Cincinnati (OH); On-site; USD 69,000 - 83,000; Full time

Job summary

Belcan Corporation in Cincinnati, OH is seeking a Quality Engineer with 6–8 years' experience in the medical device industry to lead quality, validation, and manufacturing engineering for surgical products and implants.

The role requires hands-on problem solving, data analysis, and expertise with IQ/OQ/PQ, PFMEA/DFMEA, Gage R&R, SPC/DOE, risk assessments, supplier qualification, and GMP/ISO/FDA environments; GD&T interpretation and CMM reading are a plus.

Qualifications

• Bachelor in Mechanical Engineering and 5+ years in quality/validation/manufacturing engineering in medical products.
• Medical domain experience; surgical products and implants preferred.
• GMP/ISO/FDA regulatory knowledge; Six Sigma Green/Black Belt preferred.

Responsibilities

• Ensure quality/regulatory compliance in GMP/ISO environments.
• Analyze data to drive decision making and support manufacturing.
• Lead PFMEA/DFMEA, Gage R&R, SPC, DOEs and process validations.
• Review CMM and dimensional inspection reports and GD&T.

Skills

Quality engineering

Validation methods

Manufacturing engineering

Statistical analysis

Problem solving

Education

Bachelor of Mechanical Engineering

Tools

Minitab

Excel

CMM software

Job description

Job Title: Quality Engineer

Pay Rate: $50-60/hr

Duration: 24-month contract

Location: Cincinnati, OH

Zip Code: 45242

Start Date: Right Away

Keywords: #QualityEngineerJobs

Summary:

Quality Engineer with 6 to 8 years of experience in the medical device industry, specializing in quality, validation, and manufacturing engineering for surgical products and implants. Experienced in process validation (IQ/OQ/PQ), PFMEA/DFMEA, Gage R&R, SPC, DOE, risk assessments, and supplier qualification within GMP, ISO, and FDA-regulated environments. Proficient in GD&T interpretation, dimensional data analysis, root cause investigation, and new product commercialization. Strong analytical, problem-solving, and cross-functional collaboration skills with a proven ability to drive quality, compliance, and continuous improvement initiatives.

Roles & Responsibilities:

• Experience in a GMP and/or ISO regulated medical industry is required.
• Ability to analyze and present data that facilitates & drives decision making is required.
• The ability to perform "hands on" troubleshooting and problem solving is required Experience working in an FDA regulated environment is preferred.
• Experience working in operations supporting a production environment is preferred Advanced technical training and experience using Statistics, Lean and Six Sigma Methodologies (i.e. Measurement System Analysis, SPC, DOEs, Reliability, etc.) is preferred
• Technical understanding of manufacturing equipment and processes is preferred Process Validation expertise is preferred.
• Ability to read and interpret CMM and dimensional inspection reports.
• Experience with dimensional data analysis utilizing software (Excel or Minitab)
• Experience in Medical Standards and Quality process preferred.
• New product launch experience from through full validation and commercial launch
• Experience with PFMEA/DFMEA's, Gage R&R's, TMV's, Risk Assessments and Control Plan
• Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
• Performance Component Qualification (Process Characterization, Process Capability Analysis, Test Method Validation, IQ, OQ, PQ, FAI) of new supplier manufactured components.
• Strong communication skills and ability to work well within a multidisciplinary team.
• Proficient with GD&T and interpreting technical drawings.
• Green or Black Belt Six Sigma certification preferred.

Required Qualifications:

• The Candidates should be Bachelor in Mechanical Engineering or equivalent and have min. 5 years" experience working as a Quality, Validation and or Manufacturing Engineering role in a Medical Product industry required.
• Required medical domain experience. Surgical Product and Implants experience preferred.

Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.