QC Lab Technician I

Novonesis; West Allis (WI); On-site; USD 30,000 - 42,000; Full time

Benefits offered by this job

401(k) with company contribution

Vacation time & holidays

Health, dental, vision & life 보험

HSA option

Tuition reimbursement

Wellness time

Job summary

Novonesis seeks a Quality Control Lab Technician – Human Health to support GMP‑compliant dietary supplement manufacturing. You will perform in‑house QC testing, calibrate equipment, and ensure food safety in a regulated facility with SAP/LIMS data recording.

You will contribute to product quality, regulatory compliance, and continuous improvement while collaborating with cross‑functional teams in a hands-on lab environment.

Qualifications

• The ability to read, understand, and follow SOPs, work instructions, and equipment manuals.
• Strong communication skills to collaborate with team members, cross-functional partners, and auditors.
• Basic math skills and the ability to interpret numerical data, including metric measurements and temperatures in Celsius.
• Critical thinking and problem-solving skills to adapt in a dynamic production environment.
• Experience operating laboratory and office equipment and performing basic dilution series.
• The ability to accurately interpret testing results and take appropriate action in accordance with SOPs.
• A working knowledge of GMPs and compliance standards.
• Intermediate proficiency in Microsoft Office (Word, Excel, Outlook).
• Bachelor’s degree in a scientific field or a minimum of three years of full-time experience in a laboratory environment.

Responsibilities

• Perform in-house quality control testing on samples according to SOPs and regulatory standards.
• Conduct routine equipment calibrations and verifications (scales, pH meters) to ensure accurate results.
• Follow and promote food safety and GMP requirements per FDA guidelines and internal standards.
• Record testing results, evaluations, and training in SAP and LIMS.
• Communicate testing nonconformances and observations to QC, QA, PMG, and Production teams.
• Participate in internal safety and continuous improvement initiatives (Kaizen, Lean, 5S).
• Support training and onboarding of new team members.

Skills

SOPs reading

Lab equipment operation

Quality control

Aseptic technique

Microsoft Office

Communication

Team collaboration

Education

Bachelor’s degree in a scientific field

3+ years laboratory experience

Tools

SAP

LIMS

Job description

Interested in a career that matters?Join our Human Health Quality Control team and help ensure the safety and quality of dietary supplement products that people rely on every day. In this role, you will be part of a GMP-compliant manufacturing environment where teamwork, precision, and safety are essential to meeting production and quality goals. If you enjoy hands‑on laboratory work and being part of a team that values continuous improvement, this role offers a meaningful opportunity to make an impact.

Interested in a career that matters?Join our Human Health Quality Control team and help ensure the safety and quality of dietary supplement products that people rely on every day. In this role, you will be part of a GMP-compliant manufacturing environment where teamwork, precision, and safety are essential to meeting production and quality goals. If you enjoy hands‑on laboratory work and being part of a team that values continuous improvement, this role offers a meaningful opportunity to make an impact.

The Role & Your Impact

As a Quality Control Lab Technician – Human Health, you will support quality control processes in a GMP-compliant dietary supplement manufacturing facility. Your work will directly contribute to product quality, food safety, and on-time production while supporting regulatory compliance and internal standards.

In this role, you will:

• Perform in‑house quality control testing on samples according to written SOPs, work instructions, and regulatory standards.
• Conduct routine equipment calibrations and verifications (such as scales and pH meters) to ensure accurate testing results.
• Follow and promote food safety and GMP requirements in alignment with FDA guidelines and internal certification standards.
• Use aseptic techniques to maintain sterility of media, equipment, and laboratory workspaces.
• Accurately record testing results, evaluations, and training in systems such as SAP and LIMS.
• Communicate testing nonconformances and observations to QC, QA, PMG, and Production teams.
• Participate in internal safety and continuous improvement initiatives, including Kaizen, Lean, and 5S.
• Support training and onboarding of new team members in areas of demonstrated proficiency.

What You’ll Need To Be Successful

To succeed in this role, you bring a strong attention to detail, a commitment to safety and quality, and the ability to follow structured processes in a regulated environment.

You must have:

• The ability to read, understand, and follow SOPs, work instructions, and equipment manuals.
• Strong communication skills to collaborate with team members, cross‑functional partners, and auditors.
• Basic math skills and the ability to interpret numerical data, including metric measurements and temperatures in Celsius.
• Critical thinking and problem‑solving skills to adapt in a dynamic production environment.
• Experience operating laboratory and office equipment and performing basic dilution series.
• The ability to accurately interpret testing results and take appropriate action in accordance with SOPs.
• A working knowledge of Good Manufacturing Practices (GMPs) and compliance standards.
• Intermediate proficiency in Microsoft Office (Word, Excel, Outlook).
• A Bachelor’s degree in a scientific field or a minimum of three years of full‑time experience in a laboratory environment.

Additional Skills & Interests We Value

While not required, the following are considered a plus:

• Experience working in a GMP‑regulated food, dietary supplement, or pharmaceutical environment.
• Familiarity with SAP, LIMS, or similar laboratory information systems.
• Interest in continuous improvement methodologies such as Lean, Kaizen, or 5S.
• A collaborative mindset and willingness to support teammates across functions.

What We Offer

At Novonesis, you will be part of a collaborative team that values safety, quality, and continuous improvement. We offer opportunities to learn, develop new skills, and grow within a stable manufacturing environment while contributing to products that support human health.

Ways of Working / Working Conditions

• This is an on‑site role based in Madison, Wisconsin, until January 2027, after which the position will transition to West Allis, Wisconsin. Willingness to train and work in Madison and transition to West Allis is ideal.
• Standard shift is 7:00 a.m. – 3:30 p.m., Monday through Friday.
• Weekend and hs.oliday work may be required based on production needs.
• Work is performed in a laboratory and manufacturing environment requiring adherence to hygiene, safety, and GMP standards.
• The role involves standing, routine lab work, and handling samples and equipment in accordance with safety procedure

Compensation & Benefits

Expected hourly rate: $26.00/hour

Benefits:

• 401(k) with up to a 9% company contribution
• Minimum of 3 weeks of vacation, plus 12 holidays and 2 weeks of Wellness Time
• Health, Dental, Vision & Life insurance
• Healthcare savings account option
• Employee assistance program
• Parental leave
• Tuition reimbursement
• All benefits begin on your first day!

Relevant Information

Application deadline: October 15, 2026

Location: Madison, Wisconsin (on‑site), transitioning to West Allis in January 2027

Our purpose guides the way

In Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. If our purpose resonates with you, we encourage you to apply.

Opportunities for everyone

We are committed to an inclusive recruitment process and equal opportunity for all applicants. Therefore we ask you to apply without a cover letter or photo and instead include a few sentences in your CV explaining your motivation for applying.

We make all employment decisions based on business needs and welcome candidates with a wide range of backgrounds, including ethnicity, religion, gender, sexual orientation, age, disability, or veteran status.

Explore Other Openings

If this position isn’t the right fit, you may still find other opportunities with us. You’re welcome to explore open roles or create a job agent to stay connected with future opportunities at novonesis.com/Career