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Director Quality Control Jobs in Minnesota (NOW HIRING)

Quality Control Manager

Saint Paul, MN · On-site

$120K - $140K/yr

Lead and develop the quality control team. * Ensure compliance with OSHA and workplace safety ... This is a direct hire, long term career opportunity, the starting base pay range is $120K-$140K ...

The Senior Director, Quality Operations - Clinical Chemistry Immunoassay (CCIA) North America ... Deep working knowledge of quality assurance, quality control, process validation, design quality ...

As a key member of the Quality team, the Senior Director Qualitywill be responsible for developing ... Ensure effective control of manufacturing processes, validation activities, and process monitoring ...

The Senior Director, Quality Operations - Clinical Chemistry Immunoassay (CCIA) North America ... Deep working knowledge of quality assurance, quality control, process validation, design quality ...

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Previous Leadership & management of direct reports Preferred Qualifications: * Engineering ...

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Previous Leadership & management of direct reports Preferred Qualifications: * Engineering ...

... as directed. 8. Assist with root cause investigation by providing measurement data, inspection ... experience in quality control, inspection, fabrication, machining, sheet metal, press brake ...

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Previous Leadership & management of direct reports Preferred Qualifications: * Engineering ...

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Director Quality Control information

See Minnesota salary details

$30.4K

$123K

$209.1K

How much do director quality control jobs pay per year?

As of Aug 22, 2026, the average yearly pay for director quality control in Minnesota is $123,015.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,100.00 and $147,900.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a director quality control, and how can they be addressed?

Directors of Quality Control often encounter challenges such as maintaining compliance with evolving regulatory standards, managing cross-functional teams, and ensuring consistent product quality across multiple locations. To address these challenges, it's important to stay updated on industry regulations, foster open communication between departments, and implement robust training and quality management systems. Regular audits, data-driven decision making, and strong leadership are also key to overcoming obstacles and ensuring continuous improvement within quality control operations.

What are the key skills and qualifications needed to thrive as a director quality control, and why are they important?

To thrive as a Director of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and management, typically supported by a degree in science or engineering and substantial industry experience. Familiarity with quality management systems (QMS) like ISO 9001, Six Sigma certification, and proficiency in data analysis tools are often required. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional collaboration and continuous improvement. These competencies ensure product quality, regulatory adherence, and operational excellence in highly regulated industries.

Is director quality control a good career path?

A career as a Director of Quality Control is considered stable and rewarding in industries such as manufacturing, pharmaceuticals, and food production. It involves overseeing quality assurance processes, managing teams, and ensuring compliance with industry standards, often requiring strong leadership, analytical skills, and relevant certifications. The role offers opportunities for advancement and increased responsibility with experience.

What does a director of quality control do?

A director of quality control oversees the quality assurance processes within an organization, ensuring products or services meet company standards and regulatory requirements. They develop quality policies, lead testing and inspection activities, analyze data to identify issues, and coordinate with other departments to improve quality systems. Strong leadership, analytical skills, and knowledge of industry standards are essential for this role.

What are the most commonly searched types of Quality Control jobs in Minnesota?

The most popular types of Quality Control jobs in Minnesota are:

What cities in Minnesota are hiring for Director Quality Control jobs?

Cities in Minnesota with the most Director Quality Control job openings:

Infographic showing various Director Quality Control job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 4% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $123,015 per year, or $59.1 per hour.

Full-time

Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

69th of 86 rated pharmaceutical


Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job DescriptionTitle: Associate Director, Quality ControlLocation: Brooklyn Park, MN (Onsite)About the role:

As an Associate Director, Quality Control, you will provide strategic and operational leadership for QC laboratory functions, including analytical chemistry, microbiology, bioanalytical testing, laboratory systems, and laboratory excellence. You will ensure the timely, compliant, and scientifically sound testing of raw materials, intermediates, in-process samples, and finished drug substance in support of manufacturing operations and patient needs. You will drive compliance with Takeda's Quality Management System, applicable cGMP requirements, global standards, and regulatory expectations.

You will also will partner up closely with Manufacturing and other Quality functions to advance safety, quality, compliance, operational performance, employee development, customer satisfaction, digital innovation, and continuous improvement. You will be part of the site Quality Leadership Team.

How will you contribute:
  • Lead QC laboratory operations, including analytical chemistry, microbiology, and bioanalytical functions.

  • Manage, through subordinate leaders, laboratory teams supporting routine, in-process, release, stability, and investigative testing.

  • Ensure schedule adherence and timely delivery of accurate, reliable, and scientifically justified test results.

  • Establish, implement, and maintain compliant laboratory processes, procedures, methods, and systems.

  • Ensure compliance with Takeda policies, cGMP requirements, and both local and international regulations.

  • Serve as a QC subject-matter expert during regulatory inspections, and audits.

  • Provide expertise in interpreting regulations, agency guidance, internal policies, and quality standards.

  • Support and oversee Deviation, CAPA, Change Control, Audit, and Quality Risk Management activities.

  • Conduct gap assessments and implement improvements to the Quality Management System.

  • Provide leadership for method transfers, laboratory expansion, and new product or process introductions.

  • Identify, manage, and lead continuous improvement initiatives.

  • Apply data analytics, Lean, Six Sigma, DMAIC, and other improvement methodologies where appropriate.

  • Establish and monitor QC performance metrics, including those reported through Quality Council.

  • Develop departmental budgets and ensure responsible fiscal management.

  • Plan and manage staffing, succession, training, coaching, recognition, and professional development.

  • Hire, develop, motivate, and retain technical and management personnel.

  • Communicate priorities, objectives, project timelines, and expectations effectively to staff and stakeholders.

  • Delegate responsibilities and projects based on employee capability, judgment, and experience.

  • Complete mandatory training within required timeframe.

  • Perform other duties as assigned.

What you bring to Takeda:
  • Bachelor's degree in life sciences, chemistry, engineering, or another related technical discipline required.

  • Master's degree or Ph.D. preferred.

  • 10 years of experience in pharmaceutical, biotechnology, biological-product, or regulated laboratory operations.

  • Experience leading analytical chemistry, microbiology, bioanalytical, or other multidisciplinary QC laboratory functions.

  • 6+ years of management and people-leadership experience required; experience leading large or 24/7 laboratory organizations strongly preferred.

  • Experience with regulatory inspections, audit readiness, and laboratory compliance.

  • Experience with method transfers, laboratory systems, Deviation/CAPA, Change Control, and Quality Risk Management.

  • Experience with TrackWise, SAP, Microsoft Office, and related laboratory or quality systems preferred.

  • Knowledge of endotoxin and sterility testing preferred.

  • In-depth knowledge of cGMPs, Good Data and Documentation Practices, and applicable FDA, EMA, PDA, and other regulatory requirements.

    Strong understanding of laboratory operations, analytical methods, microbiology, sterility assurance, and contamination control. Knowledge of data analytics, digital laboratory innovation, Lean, and Six Sigma concepts preferred.

  • Perform work involving moderate to high scope, complexity, and organizational impact.

  • Operate independently with general direction, applying policies, standards, scientific principles, and regulatory expectations.

  • Troubleshoot technical, operational, compliance, and quality issues and determines appropriate corrective and preventive actions.

  • Balance competing business, quality, compliance, staffing, and resource priorities.

  • Implement global QC strategies using sound scientific principles and international regulatory standards.

  • Identifie risks, escalates significant issues appropriately, and makes quality decisions aligned with Takeda policies and site procedures.

  • Build alignment and consensus with collaborators and customers across functions and organizational levels.

Other Job Requirements

  • Ability to work in controlled environments requiring special gowning and personal protective equipment.

  • May be required to work in clean rooms, confined areas, and cool or hot storage environments.

  • Ability to stand for extended periods and perform work in QC laboratory settings.

  • Requires wrist and hand motion for activities such as typing and writing.

  • May be required to work multiple shifts, weekends, or provide support for 24/7 laboratory operations.

  • Willingness to travel for meetings, training, inspections, or other business needs; approximately 5-10% travel.

  • Reasonable accommodations may be made to enable individuals with disabilities.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

Brooklyn Park, MN

U.S. Base Salary Range:

$154,400.00 - $242,550.00


The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

LocationsBrooklyn Park, MNWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Job Exempt

Yes

What Takeda Pharmaceuticals employees say

Pay

Benefits

Hours and flexibility

Workplace

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Takeda Ventures logo

About Takeda Ventures

Sourced by ZipRecruiter

Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

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