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Quality Control Associate I Jobs in Madison, WI (NOW HIRING)

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

No The Quality Associate I - Operations is the first of two levels within the QA Associate job family The associate I provides real-time QA support on the floor for GMP Manufacturing of drug product.

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

No The Quality Associate I - Operations is the first of two levels within the QA Associate jobfamily Theassociate I provides real-time QA support on the floor for GMP Manufacturing of drug product.

Ryan Companies

Quality Control Manager

Madison, WI · On-site

Ryan Companies US, Inc. has an immediate career opportunity for a Quality Control Manager to join ... Knowledge of one or more quality systems (i.e., Malcolm Baldridge, ISO 9000, Lean, Kaizen, Army ...

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Quality Control Associate I information

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How much do quality control associate i jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for quality control associate i in Madison, WI is $25.66, according to ZipRecruiter salary data. Most workers in this role earn between $18.65 and $31.25 per hour, depending on experience, location, and employer.

What is a quality control associate I?

A Quality Control Associate I is an entry-level professional responsible for ensuring that products and processes meet established quality standards in industries such as pharmaceuticals, biotechnology, and manufacturing. They perform routine inspections, tests, and analyses of materials, in-process samples, and finished goods to verify compliance with regulatory and company requirements. Additionally, they document findings, maintain laboratory equipment, and help identify areas for process improvements. This role is essential for maintaining product safety, efficacy, and consistency.

What are the key skills and qualifications needed to thrive as a quality control associate I?

To thrive as a Quality Control Associate I, you need a solid understanding of laboratory techniques, quality assurance protocols, and often a bachelor's degree in a science-related field. Familiarity with laboratory information management systems (LIMS), analytical instruments, and compliance standards such as GMP or ISO is typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring accuracy and collaborating with cross-functional teams. These skills and qualifications ensure product quality, regulatory compliance, and the overall integrity of testing processes.

What are some common challenges faced by a quality control associate I, and how can they be effectively managed?

Quality Control Associate I professionals often encounter challenges such as maintaining strict adherence to standard operating procedures, handling repetitive tasks with consistent accuracy, and managing tight deadlines for sample analysis. Effective time management and attention to detail are key to overcoming these hurdles. Collaborating with more experienced team members and actively seeking feedback can also help new associates navigate complex testing protocols and ensure high-quality results.

What cities near Madison, WI are hiring for Quality Control Associate I jobs?

Cities near Madison, WI with the most Quality Control Associate I job openings:

Quality Control Associate I jobs near you
Infographic showing various Quality Control Associate I job openings in Madison, WI as of June 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $53,366 per year, or $25.7 per hour.

Quality Control Associate Scientist- Overnight Shift

Verona, WI

Merck Group
See more jobs at Merck Groupexternal

$27 - $46/hr

Full-time

Medical, Retirement, PTO

Posted 18 days ago

Job description

Work Location: Verona, Wisconsin
Shift: 10pm-8am Monday (night)-Friday (morning)
Department: LS-SC-UYWQFD QC Release, Weekday Off-Shift
Hiring Manager: Aaron White
This information is for internals only. Please do not share outside of the organization.
Your Role:
The Madison overnight shift Scientist, Quality Associate position is responsible for the cGMP analytical laboratory analysis in the Quality Control department of MilliporeSigma. Analysis may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, method validation/qualification, cleaning, reference standard requalification, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes techniques specific to, but not limited to: HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments. Other responsibilities may include initiation and review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. The Scientist, Quality Associate position has a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.
Shift is 10pm-8am Monday (night)-Friday (morning)
Physical Attributes:
  • Work in an analytical testing lab with hazardous and toxic chemicals.

Who You Are
Minimum Qualifications:
  • Bachelor's Degree in Chemistry, Biology or other Life Science discipline.
  • 1 year in a GLP or cGMP analytical laboratory environment.

Preferred Qualifications:
  • 2+ years of experience in a GMP manufacturing or testing laboratory
  • Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7
  • Experience with chemical analyses including HPLC, GC, KF, IR, MS, and NMR,
  • Excellent written and verbal communication skills and good documentation practices and attention to detail
  • Knowledge and understanding of analytical chemistry techniques

Pay Range for this position: $27.00-$46.00 per hour.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here
RSREMD
RSREMD
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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