Find Jobs
Find Jobs Near You – Available Work in Your Location
Quality Engineer
Career Insights for Quality Control Analyst
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on North Carolina data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$73,058 / year median in North Carolina
-11% projected decline
Job Description
Quality Engineer at Commissioning Partners Quality Engineer at Commissioning Partners in Wilson, North Carolina Posted in 3 days ago.
Type:
full-time We are looking for a motivated and detail-oriented Quality Engineer to join our Quality team. This is an excellent opportunity for a recent graduate or early-career professional to build hands-on experience in a regulated manufacturing environment. The ideal candidate will support quality assurance activities, documentation, investigations, and continuous improvement initiatives while working closely with Engineering, Manufacturing, Validation, and Quality teams. Qualifications Bachelor's degree in Engineering, Life Sciences, Biotechnology, Chemistry, Pharmacy, Quality, or a related discipline. 0-2 years of experience in Quality, Manufacturing, Validation, or a regulated industry. Internship, academic project, or co-op experience in a GMP/regulated environment is a plus. Basic understanding of
GMP, FDA
regulations, and quality systems . Familiarity with documentation practices and quality processes. Strong attention to detail and organizational skills. Excellent written and verbal communication skills. Ability to work effectively in a cross-functional team environment. Proficiency with Microsoft Office, including Word and Excel . Preferred Skills GMP / cGMP Quality Management Systems (QMS) Deviations / Non-Conformances CAPA Change Control Root Cause Analysis Risk Assessment SOPs Audit Support Data Integrity / ALCOA+ FDA Regulations 21 CFR Part 11 GAMP 5