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Assistant Biotech Quality Control Jobs in Wisconsin

Novolex

Quality Control

Shawano, WI · On-site

$1.5K/day

Quality Control |Shawano |HIRING IMMEDIATELY Position Overview: Pay: $20/hr + $1.00 Shift ... Notify the Operator when product does not meet quality specifications; assist with resolution.

Novolex

Quality Control

Shawano, WI · On-site

$1.5K/day

Quality Control |Shawano |HIRING IMMEDIATELY Position Overview: Pay: $20/hr + $1.00 Shift ... Notify the Operator when product does not meet quality specifications; assist with resolution.

Novolex

Quality Control

Shawano, WI · On-site

$1.5K/day

Quality Control |Shawano |HIRING IMMEDIATELY Position Overview: Pay: $20/hr + $1.00 Shift ... Notify the Operator when product does not meet quality specifications; assist with resolution.

Novolex

Quality Control

Shawano, WI · On-site

$1.5K/day

Quality Control |Shawano |HIRING IMMEDIATELY Position Overview: Pay: $20/hr + $1.00 Shift ... Notify the Operator when product does not meet quality specifications; assist with resolution.

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Assistant Biotech Quality Control information

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

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 Assistant Biotech Quality Control jobs in Wisconsin?

For Assistant Biotech Quality Control jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Assistant Biotech Quality Control jobs in Wisconsin look for?

The top searched job categories for Assistant Biotech Quality Control jobs in Wisconsin are:

What cities in Wisconsin are hiring for Assistant Biotech Quality Control jobs?

Cities in Wisconsin with the most Assistant Biotech Quality Control job openings:

Assistant Biotech Quality Control jobs near you
Infographic showing various Assistant Biotech Quality Control job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Manager, Quality Control

PCI Pharma Services

Madison, WI • On-site

Full-time

Re-posted 28 days ago

PCI Pharma Services rating

6.3

Company rating: 6.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

492nd 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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