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Quality Control Pharma Jobs in Madison, WI (NOW HIRING)

PCI Pharma Services

QC Sample Coordinator II

Madison, WI · On-site

$20 - $27.50/hr

Quality Control / Incoming materials and samples coordinator Reporting To: Manager, Quality Control ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

PCI Pharma Services

QC Sample Coordinator II

Madison, WI · On-site

$20 - $27.50/hr

Quality Control / Incoming materials and samples coordinator Reporting To: Manager, Quality Control ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

GEA Group

Project Engineer - Pharma

Janesville, WI · On-site

$90 - $130/hr

GEA Pharma Systems is part of the GEA Group and is dedicated to innovation and thereby providing ... Co-ordinate with commercial/QC/assembly/logistics team for dispatch of material * Contributes team ...

PCI Pharma Services

QA SPECIALIST I - OPS

Madison, WI · On-site

Review and approve Manufacturing, Quality Control, and other investigations in support of batch ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

PCI Pharma Services

QA SPECIALIST I - OPS

Madison, WI · On-site

Review and approve Manufacturing, Quality Control, and other investigations in support of batch ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

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Quality Control Pharma information

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$13

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How much do quality control pharma jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for quality control pharma in Madison, WI is $21.13, according to ZipRecruiter salary data. Most workers in this role earn between $18.17 and $23.27 per hour, depending on experience, location, and employer.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Madison, WI?

For Quality Control Pharma jobs in Madison, WI, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Madison, WI look for?

The top searched job categories for Quality Control Pharma jobs in Madison, WI are:

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

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

Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Madison, WI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $43,944 per year, or $21.1 per hour.

Manager, Quality Control

PCI Pharma Services

Madison, WI • On-site

Full-time

Re-posted 26 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

444th of 545 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.
Job Description:
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-AK2
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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