QC Technician I

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

It's fun to work in a company where people truly believe in what they are doing! Neogen is seeking a detail-oriented QC Technician I to join our team. In this role, you will play an important part in supporting Neogen's manufacturing and quality operations by developing and executing quality control protocols, analyzing validation data, preparing technical reports, and helping ensure compliance with applicable regulatory requirements and internal quality standards. The ideal candidate brings experience in quality control and microbiology within a regulated environment, strong technical writing and analytical skills, and a commitment to accuracy, quality, and continuous improvement.

Work Schedule: Monday - Friday, 7:00 AM - 3:30 PM Work Model: Onsite

What You'll Do

• Develop and prepare installation, testing, and validation procedures and protocols to ensure products and processes meet regulatory requirements, Neogen standards, and industry best practices.
• Execute and support quality control activities while ensuring protocols are completed accurately and thoroughly.
• Compile, analyze, and review quality control data and prepare detailed quality reports.
• Identify trends and opportunities for improvement and recommend appropriate process enhancements.
• Conduct and support microbiological assays and prepare quality and stability reports.
• Investigate and troubleshoot quality control - and microbiology-related issues, identify root causes, and recommend effective solutions.
• Maintain accurate, organized, and complete quality control documentation and records to support compliance and traceability.
• Partner with cross-functional teams, including Manufacturing and Quality Assurance, to support quality initiatives.
• Ensure quality control activities are performed in accordance with applicable safety procedures, regulatory guidelines, and internal requirements.

What We're Looking For

• 3-5 years of experience in validation, microbiology, or a related field, preferably within a regulated manufacturing environment.
• Bachelor's degree in Microbiology, Biology, or a related scientific discipline preferred.
• Strong understanding of quality control protocols, microbiological assays, validation reporting, and regulatory compliance requirements.
• Strong analytical and problem-solving skills with the ability to investigate issues and identify root causes.
• Excellent attention to detail and organizational skills.
• Strong technical writing and documentation skills.
• Ability to collaborate effectively with cross-functional teams in a manufacturing and quality-focused environment.

Why Neogen

At Neogen , we believe taking care of our employees enables them to do their best work. When you join our team, you'll have access to competitive benefits, opportunities to grow your career, and the chance to contribute to meaningful work that makes a difference.

Benefits Include

• Benefits Starting on Day One - Medical, dental, and vision coverage begin on your first day of employment.
• 401(k) with Company Match - Invest in your future with retirement savings and company contributions.
• Paid Time Off (PTO) - Enjoy generous paid time off to rest, recharge, and spend time with those who matter most.
• Career Growth Opportunities - We're committed to developing our people and providing the tools, training, and support employees need to grow their careers.
• Meaningful Work - Be part of a team whose work has a real impact on our customers, communities, and the world around us.
• Collaborative Culture - Join an environment that values innovation, respect, teamwork, and continuous improvement.

From inside the farm gate to our dinner plates, Neogen protects the world's food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there - and you can be too.