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Biotech Quality Control Jobs in Wisconsin (NOW HIRING)

WI · On-site

Partner closely with QA/RA and QC leadership to maintain audit readiness and continuous improvement ... diagnostics, biotech). * Demonstrated ability to lead multi‑functional teams and drive ...

... and change control * Other duties as assignedeasonable accommodations may be made to enable ... Minimum 7 years of experience in medical device, pharamaceutical, or biotechnology industries with ...

WI · On-site

$100 - $125/hr

You're steering teams, balancing GMP and GAMP requirements with reality and keeping biotech ... You partner with customer the project team (Management, discipline leads, system owners, QA, ...

Showing results 41-60

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 Sep 8, 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.

What is a biotech quality control?

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 does a biotech quality control do?

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.

What are the key skills and qualifications needed to thrive in biotech quality control?

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 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:

Infographic showing various Biotech Quality Control job openings in Wisconsin as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $82,084 per year, or $39.5 per hour.

General Manager-Head of Operations, Diagnostics-TX 9056-3445 (Town of Texas)

WI • On-site

Global Recruiters of West Palm Beach
Recruiting and Staffing Services • 11 - 50 employees

Full-time

Re-posted 7 days ago


Key responsibilities

  • Lead all operational and strategic functions of the Texas site, including manufacturing, engineering, facilities, supply chain, and service/repair.

  • Develop and implement site KPIs, oversee compliance with quality and regulatory standards, and ensure audit readiness.

  • Manage site budgets, drive operational performance to meet delivery, cost, and profitability targets, and oversee hiring, training, and employee development.


Job description

Required Experience

Minimum 7 years of experience in site management or senior operations leadership within regulated manufacturing (medical devices, diagnostics, biotech).

Required Education

Masters Degree in Engineering, Business Administration, Life Sciences.

Job Description

A rapidly growing global medical diagnostics company, specializing in point‑of‑care testing, central laboratory diagnostics, enzyme manufacturing, and contract manufacturing services for the healthcare industry, is seeking a General Manager‑Site Director‑Diagnostics for its facility in Texas. The General Manager‑Site Director‑Diagnostics will lead all operational and strategic functions of the Company’s Texas site, reporting directly to the Chief Operating Officer.

Knowledge & Skills
  • Site Leadership & Operational Excellence
    • Provide overall direction and leadership for all Texas site operations including manufacturing, engineering, facilities, supply chain, and service/repair.
    • Establish a culture of accountability, teamwork, and continuous improvement.
    • Implement site KPIs to enhance structure, performance, and productivity.
  • Strategic Development & Group Alignment
    • Develop and execute long‑term strategic goals for the Texas site in alignment with the company’s Group strategy.
    • Support growth of the site’s Contract Manufacturing Organization (CMO) diagnostics business and external customer partnerships.
    • Ensure strong collaboration with the company’s global leadership and other manufacturing sites.
  • Quality, Compliance & Regulatory Standards
    • Ensure compliance with applicable quality standards, regulatory requirements, and the company’s procedures.
    • Partner closely with QA/RA and QC leadership to maintain audit readiness and continuous improvement.
    • Promote patient safety and product integrity across all operations.
  • Financial & Business Responsibility
    • Make operational financial decisions regarding budgets, cost efficiency, and capital expenditures.
    • Drive operational performance to meet delivery, cost, and profitability targets.
    • Contribute to sustainable site growth and long‑term competitiveness.
  • Cross‑Functional Collaboration (Dotted Line Functions)
    • Coordinate site execution in partnership with Quality Assurance / Quality Control, Finance, Human Resources, and IT.
    • Ensure site priorities are supported while maintaining global functional standards.
  • Other Functions
    • Ensure compliance with safety regulations and procedures; maintain a clean and safe working environment.
    • Support additional company initiatives as required.
    • Perform other duties as assigned.
  • Supervisory Responsibilities
    • Direct management responsibility for site Operations, Manufacturing, Engineering, Facilities, and Service/Repair teams.
    • Dotted‑line coordination with Quality, QC, Finance, HR, and IT.
    • Responsibilities include hiring, training, performance management, coaching, and employee development in accordance with the company’s policies and applicable laws.
Travel

Occasional travel may be required.

Work Experience, Skills and Education Required
  • Masters Degree in Engineering, Business Administration, Life Sciences, or related field.
  • Minimum 7 years of experience in site management or senior operations leadership within regulated manufacturing (medical devices, diagnostics, biotech).
  • Demonstrated ability to lead multi‑functional teams and drive operational excellence.
  • Solid understanding of ISO‑based Quality Management Systems (ISO 13485 / MDSAP preferred).
  • Strong analytical, organizational, and problem‑solving skills.
  • Excellent written and verbal communication skills in English.
Preferred Qualifications
  • MBA or advanced degree.
  • Experience in Point‑of‑Care consumables manufacturing.
  • Background in CMO/customer‑facing manufacturing operations.
  • Lean / Six Sigma Certification.
  • International leadership experience within a global matrix organization.
BASIC SKILLS AND ABILITIES
  • Detail‑oriented with strong accountability and ownership mindset.
  • Ability to manage multiple priorities in a fast‑paced environment.
  • Proven leadership and mentoring skills with a collaborative management style.
  • Strong ability to interpret business, technical, and financial information.
PHYSICAL DEMANDS & WORK ENVIRONMENT
  • Primarily office and manufacturing site environment.
  • Must be able to wear PPE as required.
  • Light physical activity with occasional movement within production and service areas.
GRN West Palm Beach

9897 Lake Worth Road, Suite 202
Lake Worth, FL 33467 USA

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