Quality Assurance Coordinator

Connexion Systems + Engineering; South Carolina; On-site; USD 31,000 - 45,000; Full time

Job summary

Connexion Systems & Engineering in Greenville, SC seeks an experienced Quality Assurance Coordinator for a 6+ month contract. The role is hands-on and supports inspection, metrology, non-conforming material handling, calibration, and regulated quality systems within a Lifecycle NPI environment.

You will perform detailed inspections to design specs, conduct incoming material checks with vision systems such as Keyence, generate NCMRs, maintain inspection records and samples, verify calibration of

Qualifications

• 5+ years of Quality Control experience in biomedical/medical device industry.
• Hands-on experience with metrology inspection equipment.
• Experience with SAP or another ERP system.
• Regulated quality systems know-how: ISO 9001:2015, ISO 13485:2016, 21 CFR 820.
• Proficient with inspection tools such as calipers, gauges and related equipment.

Responsibilities

• Perform detailed product inspections in accordance with SOPs and design specs.
• Conduct incoming material inspections using vision inspection systems, including Keyence.
• Generate and document Non-Conforming Material Reports (NCMRs).
• Create, maintain, and organize inspection records and retain samples.
• Verify inspection and test equipment is properly calibrated.
• Use problem-solving to identify opportunities for process improvement.
• Support additional quality-related activities and projects as assigned.

Skills

Quality control experience

Metrology inspection

SAP / ERP systems

Inspection tools

Excel & Word

Teamwork

Problem solving

Attention to detail

Education

High School Diploma or equivalent

Tools

SAP

Keyence vision system

Calipers & gauges

Job description

Title: Quality Assurance Coordinator

Hiring Organization: Connexion Systems & Engineering

Compensation, Benefits, and Employment Type: 6+ months contract, Pay rate: up to $27.58/hr based on experience

Job Location: Greenville, SC

Work Model: 100% onsite

Schedule: Monday – Friday, 1st shift

Job#: bh19601

A leading biomedical manufacturing organization is seeking an experienced Quality Assurance Coordinator to support quality control and inspection activities within a Lifecycle NPI environment. This is a hands‑on quality role for someone with strong experience in inspection, metrology, non‑conforming material, calibration, and regulated quality systems.

What You'll Do

• Perform detailed product inspections in accordance with SOPs and design specifications.
• Conduct incoming material inspections using vision inspection systems, including Keyence.
• Generate and document Non-Conforming Material Reports (NCMRs) when products or materials do not meet specifications.
• Create, maintain, and organize inspection records and retain samples.
• Verify inspection and test equipment is properly calibrated.
• Use critical thinking and problem‑solving skills to identify opportunities for process improvement.
• Support additional quality-related activities and projects as assigned.

What We're Looking For

• 5+ years of Quality Control experience in the biomedical/medical device industry.
• Hands‑on experience with metrology inspection equipment.
• Experience with SAP or another ERP system.
• Working knowledge of regulated quality systems, including: ISO 9001:2015 ISO 13485:2016 21 CFR 820
• Proficiency with inspection tools such as calipers, gauges, and related measurement equipment.
• Strong attention to detail and ability to identify quality issues.
• Excellent problem‑solving, organizational, written, and verbal communication skills.
• Proficiency with Microsoft Excel and Word.
• Ability to work effectively in a team environment.
• Ability to lift and/or move up to 50 lbs.

Education

High School Diploma or equivalent required.

Why Consider This Opportunity

Join a quality‑focused team within a regulated biomedical manufacturing environment. Gain exposure to new product introduction (NPI), inspection, metrology, and quality systems. Contract opportunity with potential for valuable industry experience. Monday–Friday schedule with a consistent 40‑hour workweek.