Quality Engineer

Commissioning Partners; Wilson (NC); On-site; USD 52,000 - 78,000; Full time

Job summary

Commissioning Partners is seeking a motivated Quality Engineer to join our Quality team in a regulated manufacturing environment. This early-career opportunity offers hands-on experience across QA activities, documentation, investigations, and continuous improvement.

You will work closely with Engineering, Manufacturing, Validation, and Quality teams to ensure GMP compliance and robust quality systems, while building a strong foundation for a career in quality engineering.

Qualifications

• Bachelor's degree in Engineering or related disciplines.
• 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.
• Excellent written and verbal communication skills.
• Ability to work effectively in a cross-functional team environment.
• Proficiency with Microsoft Office, including Word and Excel.

Responsibilities

• Support quality assurance activities.
• Assist documentation and investigations.
• Contribute to continuous improvement initiatives.
• Collaborate with Engineering, Manufacturing, Validation, and Quality teams.

Skills

Attention to detail

Communication skills

Cross-functional collaboration

Education

Bachelor's degree

Tools

Microsoft Word

Microsoft Excel

Job description

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.