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Biotech Quality Control Jobs in Wisconsin (NOW HIRING)

Elephas

General Supervisor - CAP/CLIA Lab

Madison, WI · On-site

Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated ... Review and approve quality control data, taking corrective action when necessary. * Monitor ...

Elephas

General Supervisor - CAP/CLIA Lab

Madison, WI · On-site

Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated ... Review and approve quality control data, taking corrective action when necessary. * Monitor ...

Elephas

General Supervisor - CAP/CLIA Lab

Madison, WI · On-site

Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated ... Review and approve quality control data, taking corrective action when necessary. * Monitor ...

Elephas

General Supervisor - CAP/CLIA Lab

Madison, WI · On-site

Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated ... Review and approve quality control data, taking corrective action when necessary. * Monitor ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Wisconsin

Biotech Quality Control information

See Wisconsin salary details

$30.8K

$82.1K

$130.7K

How much do biotech quality control jobs pay per year?

As of Jul 16, 2026, the average yearly pay for biotech quality control in Wisconsin is $82,084.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,100.00 and $100,900.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in Wisconsin? The most popular types of Biotech Quality Control jobs in Wisconsin are:
What are popular job titles related to Biotech Quality Control jobs in Wisconsin? For Biotech Quality Control jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Wisconsin look for? The top searched job categories for Biotech Quality Control jobs in Wisconsin are:
What cities in Wisconsin are hiring for Biotech Quality Control jobs? Cities in Wisconsin with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Wisconsin as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 87% Full Time, 5% Part Time, 2% Temporary, and 4% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $82,084 per year, or $39.5 per hour.
Supervisor, Quality Assurance Internal Operations

Supervisor, Quality Assurance Internal Operations

PCI Pharma Services

Madison, WI • On-site

Full-time

Re-posted 20 days ago

PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

436th of 528 rated manufacturers

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Responsible for leading QA Associates, who provide QA support in the manufacturing of clinical and commercial drug products, to ensure compliance with the principles and guidelines of cGMP. The Supervisor, QA Ops assists in maintaining quality systems, management of investigations, materials management and providing QA support in real time for manufacturing, to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner.
Essential Duties and Responsibilities:
  • Provide QA support for cGMP manufacturing operations.
  • Coordinate with cross-functional teams to continually improve procedures with respect to area line clearances, labeling, packaging and material release.
  • Support QA scheduling activities by monitoring the production, and visual inspection schedules and project management deliverables, and reviewing factors that may impact schedules.
  • Oversee Quality System Events (QSEs) by verifying a Quality reviewer has been assigned to the QSE and monitor that the QSEs are being completed on time. Assist where needed.
  • Lead Associates in providing QA on the floor oversight of manufacturing.
  • Oversee and assist employees with product / material labeling and disposition functions, routine manufacturing area line clearances, AQL Sampling and Inspection of Final Package Lots.
  • Supervise the employees in the Quality Assurance Department.
  • Ensure all training is performed by employees, including aseptic gowning, facility flow and visual
  • inspection.
  • Maintain Quality Metrics for the company.
  • Review of master and executed raw material records. Release raw materials, as necessary.
  • Review of associated QC data to support facility and products, as applicable
  • 12. Review Quality logbooks, as applicable.
  • 13. Responsible for writing and revising Standard Operating Procedures, specifications, material control
  • procedures, deviations, CAPA's, and Quality Investigations when applicable.
  • Direct involvement in supporting external client audits at PCI and regulatory inspections, and responsible for responding to audit observations, as applicable.
  • Obtain gown qualification for sterile manufacturing line clears.
  • Assist with Change Control, as needed
  • Maintain and evaluate procedures and monitor new regulations.
  • This position may require overtime and/or weekend work.
  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
  • Attendance to work is an essential function of this position
  • Performs other duties as assigned by Manager/Supervisor.

Qualifications:
Required:
  • BS degree in a scientific discipline
  • Minimum 5+ year's relevant GMP experience.
  • Knowledge of FDA/ISO regulatory requirements as well as industry trends.
  • Computer knowledge, including Microsoft Office, Windows.
  • Excellent interpersonal skills, must be able to lead and make decisions.
  • College Level Mathematical Skills

Preferred:
  • Experience supporting manufacturing and conducting training is preferred.
  • Previous supervisory experience is preferred.
  • Experience executing GMP quality systems in a pharmaceutical/biotech/medical device environment preferred.

#LI-LL1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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