ZipRecruiter

Log In

1

Biotech Quality Control Jobs in Wisconsin (NOW HIRING)

PSG Global Solutions

Quality Assurance

Middleton, WI

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... QC inspection, Maintain training system Qualifications * Hard working and competent * 3-5 years of ...

Iff

Quality Analyst

Beloit, WI

Support quality control processes by identifying deviations and escalating issues as needed ... Experience working with enzyme production or industrial biotechnology processes * Familiarity with ...

next page

Showing results 1-20

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.
Manager, Quality Control

Manager, Quality Control

PCI Pharma Services

Madison, WI • On-site

Full-time

Posted 13 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.
This position is responsible for the daily QC oversight of PCI's laboratory functions. This includes all operational and technical activities in delivering quality chemical, biopharmaceutical and microbiologic testing services to our customers. This position oversees core activities such as in process testing and micro testing. The role includes oversight of raw material, in process, and reviewing release testing of GMP products to support our clients, interacting with Clients concerning project specific QC issues, approving department cGMP documents, contributing to cGMP reports, and managing QC staff as necessary to achieve these tasks.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related investigations (deviations, OOS/OOT, EM Investigations, etc.) both with internal and external laboratories
  • Maintains good relations and communications with clients as a primary technical interface
  • Interact with customers to identify opportunities to improve quality and establish feedback with manufacturing personnel
  • Interface with supplier and customer quality representatives concerning problems with quality control and assure that effective corrective action is implemented
  • Working with project teams to represent Quality Control, conducting risk assessments and introducing best practices into the Quality Control processes
  • Leading customer interaction on all QC related projects including routine testing updates
  • Manage and develop professional and technical skills and performance of department members
  • Assure all QC functions and testing are being performed according to FDA, EMA, ICH and other international regulations, as deemed necessary
  • Supporting regulatory information requests from customers as it pertains to QC. Supporting Operations, Project Management Staff and Quality Assurance as needed
  • Drive technical troubleshooting, operational improvements, and efficiency improvements while working within cGMP and global regulatory compliance
  • Demonstrate substantial knowledge of subject matter, industry best practices and trends
  • Other tasks as assigned by management.

QUALIFICATIONS:
Required:
  • BS in Chemistry, Biochemistry, Microbiology, Biology or related life sciences field. Advanced level degree preferred
  • 5+ years of Pharmaceutical or Biotechnology industry experience
  • Experience in leading a commercial, aseptic drug product quality control team,
  • 5+ years previous QC management experience
  • Quality leadership experience working on cross-functional teams to harmonize operational, testing and compliance processes
  • Experience in the Management of +5 people

Preferred:
  • Prior experience in a CMO or dealing with CMOs preferred
  • Demonstrates excellent verbal, written, and interpersonal communication skills
  • Demonstrated ability to perform in a fast-paced environment
  • Highly developed leadership capabilities to motivate and inspire teams
  • Independently motivated, detail oriented and good problem-solving ability.
  • Demonstrates a strong customer service orientation with effective follow through
  • Driven to excellence while encouraging others to engage in process improvement and innovation
  • A leader who inspires and motivates, through excellent listening skills and a willingness to mentor team members

#LI-RS1
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.

What PCI Pharma Services employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply