WHY JOIN US?

Because here, quality isn’t just a requirement—it’s our reputation. If you’re passionate about precision, thrive on problem-solving, and want to see your work make a real impact, this is your chance to shine.

QUALIFICATIONS:

• Bachelor’s degree in Mechanical Engineering or related field of study.
• Proven experience in quality engineering, preferably in a manufacturing environment.
• Strong understanding of quality standards and methodologies (e.g., ISO 9001, ISO 13485, ASTM, Six Sigma).
• Experience in a regulated manufacturing environment is required; experience in medical device, food, or aerospace is a plus.
• Proficiency with mechanical inspection tools and techniques.
• Familiarity with engineering drawings, specifications, and GD&T (Geometric Dimensioning and Tolerancing).
  Job Type: Full-time
  Pay: $85,000.00 - $90,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Application Question(s):

• Please provide current salary requirements (a range is acceptable; however N/a or blank may result in disqualification from consideration).
• Will you now, or in the future, require sponsorship (i.e. H-1B visa, etc.) to legally work in the U.S.?

Education:

• Bachelor’s (Required)

Location:

• Verona, VA 24482 (Preferred)

Ability to Commute:

• Verona, VA 24482 (Required)

Ability to Relocate:

• Verona, VA 24482: Relocate before starting work (Required)

Work Location: In perso

WHERE PRECISION MEETS PURPOSE!

Cutting edge quality starts with you! Our client, AccuTec, Inc. is looking for a Quality Engineer to oversee and elevate the quality of our manufacturing processes for industrial, food, and medical blades.
This isn’t just about inspections and checklists—it’s about being a quality leader who ensures our products exceed expectations, meet regulatory standards, and set the bar in our industry. You’ll collaborate across departments, solve challenges with innovation, and champion continuous improvement that keeps us at the cutting edge. This is where precision meets purpose.

WHAT YOU’LL DO:

• Lead inspections, audits, and testing to guarantee compliance and customer confidence
• Partner with cross-functional teams to streamline processes and enhance efficiency
• Take ownership of quality issues, delivering solutions that last
• Drive a culture of continuous improvement, ensuring every product reflects excellence

KEY RESPONSIBILITIES:

• Quality Assurance & Control: Develop, implement, and maintain quality assurance processes for all products. Monitor and evaluate production processes to ensure they meet both internal and external quality standards.
• Testing and Inspection: Perform inspections of products, parts, and systems using measuring tools such as calipers, micrometers, and CMM machines. Oversee mechanical testing procedures including stress tests, performance tests, and material validation.
• Root Cause Analysis & Problem Solving: Investigate quality issues and customer complaints to determine root cause. Implement Corrective and Preventative Actions (CAPA) and work with production and engineering teams to resolve problems. Utilize problem-solving tools such as 8D, Fishbone Diagrams, and FMEA to address quality concerns.
• Process Improvement: Lead and participate in continuous improvement initiatives to enhance product quality and manufacturing efficiency. Collaborate with design and production teams to optimize product design, materials, and manufacturing processes. Implement Lean and Six Sigma methodologies to optimize production and reduce defects.
• Documentation & Reporting: Maintain detailed records of quality inspections, test results, and non-conformance reports. Create and maintain quality documentation such as control plans, work instructions, and procedures. Generate quality reports, present findings, and recommend improvements to management.
• Supplier Quality Management: Ensure that materials and components from suppliers meet the required quality standards. Conduct supplier assessments, audits, and performance reviews to maintain a high-quality supply chain.
• Regulatory Compliance: Ensure all products comply with industry-specific standards and regulatory requirements. This includes ISO 9001, and ISO 13485 for medical devices. Participate in regulatory audits and provide the necessary documentation for compliance purposes.