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Quality Control Investigator Jobs in Minnesota (NOW HIRING)

Quality Control Chemist (Overnight Shift) The Quality Control Chemist performs testing and ... Troubleshoot out-of-specification (OOS) situations by investigating potential causes and working ...

New

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Investigation and data analysis skills HOYA Group : Founded in 1941 in Tokyo, Japan, HOYA ...

QC Chemist

Baudette, MN · On-site

$48K - $52K/yr

Quality Control Chemists must successfully complete the following training: Policy and Standard ... Prepare PPA's, investigation reports, and Method/SOP/IOP revisions. 5. 5% Performs other duties as ...

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Investigation and data analysis skills HOYA Group : Founded in 1941 in Tokyo, Japan, HOYA ...

Supporting the development and training of QC personnel to enhance inspection skills, knowledge of ... Investigation and data analysis skills About Us HOYA Group : Founded in 1941 in Tokyo, Japan, HOYA ...

Quality Control Chemists must successfully complete the following training: Policy and Standard ... Prepare PPA's, investigation reports, and Method/SOP/IOP revisions. 5. 5% Performs other duties as ...

Quality Control Inspector Schedule: B: Monday - Thursday, 5pm - 3:30am Pay Range: $20.00 - $25.00 ... Support investigations into quality issues and participate in root cause analysis and corrective ...

Quality Control Inspector

Blaine, MN · On-site

$20 - $25/hr

Quality Control Inspector Schedule: B: Monday - Thursday, 5pm - 3:30am Pay Range: $20.00 - $25.00 ... Support investigations into quality issues and participate in root cause analysis and corrective ...

Quality Control Technician

Oakdale, MN · On-site

$19.25 - $24.50/hr

May also investigate and troubleshoot problems and determine solutions. Maintains validation ... QC issues * Adheres to GLP/ISO guidelines in daily activities * Other duties as may be assigned by ...

... root cause investigations, and supporting qualification activities. You will act as a key ... control methods to monitor and improve processes * Collaborate with customer Quality and NPI ...

Quality Control Engineer

Sauk Rapids, MN · On-site

$86K - $110K/yr

... root cause investigations, and supporting qualification activities. You will act as a key ... control methods to monitor and improve processes * Collaborate with customer Quality and NPI ...

Q3 Contracting, has an immediate opening for a Quality control Specialistin Little Canada, MN ... Accident and/or incident investigation & reporting. * Provides direct engagement with crew ...

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Quality Control Investigator information

What is a quality control investigator?

Quality Control Investigators are professionals responsible for ensuring that products or services meet established quality standards and regulatory requirements. They inspect processes, materials, and finished goods, investigate quality issues, and recommend corrective actions to prevent recurrence. Their work is crucial in maintaining product safety, consistency, and compliance across various industries, such as manufacturing, pharmaceuticals, and food processing.

What are the key skills and qualifications needed to thrive as a quality control investigator?

To thrive as a Quality Control Investigator, you need expertise in quality assurance processes, attention to detail, and a background in science or engineering, often supported by relevant certifications such as Six Sigma or ISO compliance. Familiarity with laboratory equipment, statistical analysis software, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication are essential soft skills in this role. These competencies ensure that products and processes consistently meet regulatory standards and company expectations, minimizing errors and maintaining organizational integrity.

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

Quality Control Investigators often encounter challenges such as managing tight deadlines for investigating quality deviations, ensuring thorough documentation, and coordinating with multiple departments to collect necessary information. To address these, it's important to develop strong organizational skills, maintain clear communication channels, and stay current with regulatory requirements. Proactively collaborating with production, QA, and regulatory teams can help streamline investigations and lead to more effective root cause analysis and corrective actions.

What is the difference between Quality Control Investigator vs Quality Assurance Specialist?

AspectQuality Control InvestigatorQuality Assurance Specialist
CertificationsOften requires GMP, GLP, or ISO certificationsSimilar certifications, with additional focus on auditing
Work EnvironmentLaboratory, manufacturing, or production settingsOffice, laboratory, or production environments
Primary FocusInvestigating quality issues, deviations, and non-conformancesDeveloping and implementing quality systems and procedures
Employer & Industry UsagePharmaceutical, biotech, manufacturingPharmaceutical, biotech, manufacturing

Both roles are vital in quality management, but the Quality Control Investigator primarily focuses on identifying and resolving quality issues through investigations, while the Quality Assurance Specialist develops systems to prevent issues. They often work together to ensure product quality and compliance.

What are popular job titles related to Quality Control Investigator jobs in Minnesota?

For Quality Control Investigator jobs in Minnesota, the most frequently searched job titles are:

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

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

Infographic showing various Quality Control Investigator job openings in Minnesota as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

$120K - $145K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Job description

Description

WHO WE ARE

We are a growing medical device company developing innovative technology to transform the treatment of mitral valve disease. Our team is advancing a Class III structural heart device through pivotal clinical trials, with a shared focus on delivering a high-quality product that can make a meaningful difference for patients.


 At 4C Medical, you'll find an environment where your ideas matter, your growth is prioritized, and your contributions directly influence our success. We're committed to fostering both personal and professional development in a culture built on accountability, curiosity, and shared purpose. 


THE OPPORTUNITY

We are seeking a Quality Control Manager to lead day-to-day QC operations for our highly specialized medical device manufacturing environment. This is a hands-on leadership opportunity where you will oversee inspection, testing, compliance, and quality activities across complex processes including tissue processing, valve assembly, Nitinol frame shape-setting, delivery system fabrication, and cleanroom packaging.

You will lead a team of five quality engineering and inspection professionals while helping ensure the organization remains audit-ready as we progress toward commercial approvals in the U.S., Europe, and Canada.


HOW YOU WILL CONTRIBUTE

QC Operations & Assembly Support: Oversee daily inspection, testing, and release operations for raw materials, in-process components, and finished sterile devices. Drive rigorous quality oversight for the high-precision tissue-to-frame sewing and valve assembly processes.

Audit Readiness & Compliance: Maintain a continuous state of audit readiness across the QC footprint. Ensure documentation, traceabilities, and processing environments comply with FDA, CE Mark, and Health Canada regulations.

Non-Conformance & CAPA Management: Own the investigation, root-cause analysis, and disposition of non-conformances (NCMRs) and deviations. Directly handle failures or anomalies identified during complex valve assembly and sewing operations.

Team Leadership & Development: Directly manage, mentor, and resource-load the QC team. Partner with the Quality Training Coordinator to ensure the highly specialized training and qualification matrices required for valve sewing and assembly are meticulously maintained.

Process & Environmental Control: Oversee environmental monitoring, bioburden testing, and cleanroom compliance for the in-house tissue fixation, processing, and device assembly lines.

Supplier Quality Oversight: Support the Sr. Supplier Quality Engineer in managing critical component vendors, resolving supplier corrective actions (SCARs), and coordinating incoming inspection criteria.

Requirements


WHAT YOU NEED TO SUCCEED (MINIMUM QUALIFICATIONS)
  • Bachelor's degree in Engineering, Life Sciences, Quality, or a related technical field.
  • 7+ years of experience in quality control, quality engineering, manufacturing quality, or a related medical device environment.
  • Experience working within FDA-regulated medical device manufacturing and a strong understanding of 21 CFR Part 820 and ISO 13485.
  • Experience leading investigations, non-conformances, CAPA, and root-cause analysis.
  • Experience managing, mentoring, and developing quality professionals.
  • Strong understanding of inspection, testing, process controls, and quality systems within a manufacturing environment.
  • Ability to work effectively in a hands-on, fast-paced environment and manage multiple priorities.
WHAT WILL SET YOU APART (COMPETENCIES)
  • Experience with Class III medical devices, particularly implantable or structural heart products.
  • Experience with tissue processing, tissue sewing, valve assembly, or other highly specialized medical device manufacturing processes.
  • Experience supporting pivotal clinical trials and/or commercialization activities.
  • Familiarity with MDSAP, CE Mark, and Health Canada regulatory requirements.
  • Experience working in cleanroom environments and with environmental monitoring or bioburden testing.
  • Strong leadership and team development skills with the ability to balance hands-on problem solving with strategic thinking.
  • Excellent communication and collaboration skills with the ability to influence across functions.
  • Demonstrated ability to thrive in an entrepreneurial environment where priorities can evolve and individuals are expected to roll up their sleeves and get things done.
WHY JOIN US

We recognize that meaningful work is supported by meaningful benefits. That's why we offer a competitive compensation package along with comprehensive benefits designed to support you and your family's health, well-being, and financial future.Our benefits package includes:

  • Medical
  • Dental
  • Vision
  • Flexible Spending Account (FSA)
  • Basic Life 
  • 401(k) Retirement Plan
  • Paid Holidays
  • PTO
  • Maternity/Paternity paid leave

It is 4C Medical's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state or local laws. Â