Onsite QC Technician I – Microbiology & Validation

neogen; Lansing (MI); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401(k) with match

Paid time off

Career growth

Meaningful work

Collaborative culture

Job summary

Neogen is seeking a detail-oriented QC Technician I to support manufacturing and quality operations by developing and executing QC protocols, analyzing validation data, and preparing technical reports.

You will assist with microbiological assays, investigate issues, and ensure compliance with regulatory requirements and internal standards. The role emphasizes accuracy, quality, and continuous improvement in an onsite setting.

Qualifications

• 3-5 years of experience in validation, microbiology or related field in a regulated environment.
• Strong written and verbal communication skills for technical reports and documentation.
• Ability to identify root causes and implement corrective actions.
• Experience with regulatory compliance and quality standards.

Responsibilities

• Develop and prepare QC procedures and validation protocols to meet regulatory requirements and Neogen standards.
• Execute QC activities and ensure protocols are followed accurately.
• Compile, analyze, and review QC data and produce detailed reports.
• Identify trends and recommend process improvements.
• Conduct and support microbiological assays and generate quality and stability reports.
• Investigate QC and microbiology issues, determine root causes and propose solutions.
• Maintain organized QC documentation for traceability and compliance.
• Collaborate with Manufacturing and Quality Assurance to support quality initiatives.
• Ensure safety procedures and internal requirements are followed.

Skills

Quality control

Microbiology

Technical writing

Analytical skills

Problem solving

Education

Bachelor's degree in Microbiology

Tools

Laboratory equipment

Job description

Neogen is seeking a detail-oriented QC Technician I to support manufacturing and quality operations by developing and executing QC protocols, analyzing validation data, and preparing technical reports.

You will assist with microbiological assays, investigate issues, and ensure compliance with regulatory requirements and internal standards. The role emphasizes accuracy, quality, and continuous improvement in an onsite setting.