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Quality Control Program Manager Jobs in Delano, MN

kurt

Quality Manager

Minneapolis, MN

$110K - $143K/yr

The Quality Manager plans, coordinates and directs the quality control program designed to ensure continuous production of products consistent with established standards. Applicants must be currently ...

Intellectt INC

QA/QC Inspector

Minnetonka, MN · On-site

Role: QA/QC Inspector Location: Minnetonka, MN - 55345 Duration: 6 Months Shift Timings: 8:30 AM to ... Quality Management Systems (QMS), Environmental Management Systems (EMS), and other applicable ...

Takeda

Quality Control Analyst II

Brooklyn Park, MN

$25 - $33.50/hr

Must be able to communicate effectively with managers and peers. * Must be able to read, write, and ... programs. Takeda is a patient-focused company that will inspire and empower you to grow through ...

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All JobsQuality Control Program JobsQuality Control Program Manager JobsQuality Control Program Manager Jobs in Delano, MN

Quality Control Program Manager information

See Delano, MN salary details

$31.9K

$85.2K

$135.6K

How much do quality control program manager jobs pay per year?

As of Jul 14, 2026, the average yearly pay for quality control program manager in Delano, MN is $85,156.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,400.00 and $104,700.00 per year, depending on experience, location, and employer.

What does a QA manager earn?

A Quality Control Program Manager typically earns a salary ranging from $70,000 to $130,000 annually, depending on experience, industry, and location. They often hold certifications such as Six Sigma or ISO auditor credentials and require strong leadership and analytical skills to oversee quality assurance processes.

What are the key skills and qualifications needed to thrive as a Quality Control Program Manager, and why are they important?

To thrive as a Quality Control Program Manager, you need expertise in quality assurance methodologies, data analysis, and process improvement, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), Six Sigma certification, and proficiency in statistical software are typically required. Strong leadership, problem-solving abilities, and effective communication skills help you lead teams and drive compliance. These competencies are crucial to ensure product quality, regulatory adherence, and continuous organizational improvement.

What does a quality program manager do?

A quality program manager oversees the development, implementation, and maintenance of quality assurance programs within an organization. They coordinate cross-functional teams, monitor quality metrics, and ensure compliance with industry standards and regulations, often using tools like quality management systems. Their role involves continuous improvement initiatives to enhance product or service quality and customer satisfaction.

What are Quality Control Program Managers?

Quality Control Program Managers are professionals who oversee and coordinate quality assurance activities within an organization. They develop, implement, and maintain quality control systems to ensure that products or services meet established standards and regulatory requirements. These managers lead teams, conduct audits and inspections, analyze quality data, and collaborate with other departments to resolve quality issues. Their role is critical in minimizing defects, improving processes, and ensuring customer satisfaction.

What is the difference between Quality Control Program Manager vs Quality Assurance Specialist?

AspectQuality Control Program ManagerQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, Six SigmaISO 9001 Internal Auditor, Six Sigma Green Belt
Work EnvironmentOversees quality control processes across projects, often in manufacturing or production settingsFocuses on developing and implementing quality assurance procedures, typically in labs or office settings
Employer & Industry UsageManufacturing, aerospace, automotive, constructionPharmaceuticals, software, manufacturing, healthcare

The Quality Control Program Manager primarily manages and oversees quality control processes to ensure products meet standards, while the Quality Assurance Specialist develops and maintains quality assurance systems to prevent defects. Both roles require similar certifications and work in related environments, but their focus differs: control vs. assurance.

What does a quality control manager do?

A quality control program manager oversees the development and implementation of quality standards and procedures to ensure products or services meet specified requirements. They conduct inspections, analyze data, and coordinate with teams to improve quality processes, often using tools like statistical analysis and quality management systems. The role requires strong attention to detail, leadership skills, and knowledge of industry regulations.

What career paths are possible in QC?

A Quality Control Program Manager can advance to roles such as Quality Director, Quality Assurance Manager, or Operations Manager, often by gaining experience and certifications like Six Sigma or ISO auditor credentials. They may also specialize in areas like supplier quality, compliance, or process improvement, expanding their career opportunities within manufacturing, healthcare, or technology industries.

How does a Quality Control Program Manager typically collaborate with cross-functional teams to ensure product standards are met?

A Quality Control Program Manager regularly works alongside teams such as manufacturing, engineering, regulatory affairs, and supply chain to align quality standards across all stages of production. This collaboration often involves participating in cross-functional meetings, reviewing process documentation, and leading corrective action initiatives when deviations occur. By fostering open communication and implementing feedback loops, the manager ensures that quality objectives are understood and met company-wide, minimizing errors and supporting continuous improvement.
Quality Control Program Manager jobs near you
Quality Control Technician

Quality Control Technician

PROMED MOLDED PRODUCTS INC

Minneapolis, MN • On-site

$31.04 - $41.05/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

As a ProMed employee, you will contribute to the manufacture of products that have a significant impact on people’s lives. Through honesty, integrity, and collaboration, we strive to be the very best as we hire the very best.


ProMed was founded in 1989 addressing an industry need for cleanroom manufacturing of silicone components, specifically those having a medical application. We treat every component and finished device as though it will be used by a beloved family member or friend. We are dedicated to our customers and to our employees while helping to improve the health and well-being of people around the world.


Working as one to help many.


POSITION SUMMARY

The Quality Technician is responsible for day-to-day administration and support as applicable to the organization’s environmental monitoring, preventative maintenance and calibration, facilities control, material management, pharmaceutical operations and cleaning verification/validation. This position operates under minimal guidance from management or senior staff. The Quality Technician ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed.


ESSENTIAL DUTIES & RESPONSIBILITIES

Position duties and responsibilities include, but are not limited to the following:


  • Perform and document routine environmental monitoring of cleanrooms and controlled areas and test/send samples to approved testing laboratories.
  • Interpret sampling results, maintain trending spreadsheets, and complete data review forms.
  • Author (annual) trend reports.
  • Standardize/Assist with updating sampling maps in the event of room changeover.
  • Coordinate with Facilities for scheduling of and accompany cleanroom certification/testing contractors.
  • Maintain inventory of consumable testing supplies, submit purchase requisitions to restock.
  • Monitor DicksonOne and address/assist with any excursions.
  • Review and trend preventative maintenance and calibrations.
  • Review and trend pest control logs, vendor reports and issues.
  • Perform cleaning verification/validation swabbing and submit samples to analytical lab for testing.
  • Perform sampling of materials for QC testing, retains, and retesting.
  • Assist with incoming material inspection records.
  • Assist in updating or revision SOPs/forms/templates for clarity and accuracy.
  • Review of logbooks.
  • Assist with line clearance and checks.
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OTHER RESPONSIBILITIES

  • Identify and escalate gaps, inconsistencies, or potential compliance risks within the QMS to the QA Manager.
  • Participate in internal audits and self-inspections as assigned; support corrective action follow-up activities.
  • Support the implementation of regulatory changes and quality system improvements as directed;
  • Assist in preparing responses to audit observations or regulatory findings that involve document or records management.

This job also requires performing other duties as assigned.



QUALIFICATION, EDUCATION & EXPERIENCE

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


Required:

  • Bachelor’s degree in Life Sciences, Chemistry, Microbiology, or a related field.
  • 0-3 years of experience in a regulated industry (pharmaceutical or biotech).
  • Knowledge of GMP principles and FDA regulatory requirements (21 CFR Parts 210/211 and/or 820).
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Knowledge of ALCOA+ data integrity principles.


Preferred:

  • Familiarity with eQMS platforms (e.g., MasterControl, Veeva Vault, Agile, TrackWise) even if primary system is paper-based.
  • Experience with EU GMP, ICH Q7, ICH Q2(R1), and/or ISO 13485 requirements.
  • Ability to work autonomously, effectively manage time and deliver results on time.
  • Attention to detail and commitment to data integrity and accuracy in all quality records.
  • Effective written and verbal communication skills; ability to clearly document processes, decisions, and deviations.
  • Strong organizational skills with the ability to manage multiple priorities, deadlines, and document workflows simultaneously.
  • Collaborative mindset with the ability to work cross-functionally with operations, R&D, and other QA functions.
  • Comfort working in a structured, compliance-driven environment with defined SOPs and change control requirements.
  • Proactive problem-solving skills; escalates issues appropriately and follows through on assigned action items.
  • Aptitude for learning and applying regulatory requirements and quality standards.


WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the principal roles and responsibilities of this job:

  • Exposure to heated/air conditioned, ventilated facilities with florescent lighting;
  • Exposure to building where a variety of chemical substances are used for cleaning, and/or operation of equipment;
  • The noise level in the work environment is usually minor;
  • Duties are performed indoors;
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

PHYSICAL, SENSORY, COGNITIVE & NEUROLOGICAL DEMANDS

While performing the duties of this job:

  • The employee may be required to stoop, bend, squat, kneel, reach, stand, walk, lift, pull, push, grasp, talk, hear, see and use repetitive motions;
  • Specific vision abilities required include close vision such as to read handwritten or typed material and the ability to adjust focus;
  • The position requires the individual to meet multiple demands from several people and interact with internal and external people;
  • Employee moves about the building and be able to maneuver in tight spaces between desks, etc.;
  • Employee may have duties involving walking on even or uneven surfaces;
  • Employee occasionally to frequently use a whiteboard, which can require grasping whiteboard pens, reaching at, below, or above shoulder height and may require trunk or neck rotation to look back;
  • Employee may use computers, overhead projectors, TV, and other work-related equipment, which may require an approximately 25+ pound force to push or pull equipment;
  • It is necessary to grasp and manipulate pens, markers, scissors, staplers, etc. occasionally to frequently;
  • Employee must see and hear on a continuous basis as well as speak frequently;
  • Position varies from standing, sitting, walking, etc. On some occasions it may be necessary to move quickly, run, etc. over smooth or uneven surfaces.


ProMed offers a generous benefits package including:

  • 401k with company match
  • Profit Sharing Program
  • Medical Insurance
  • Health Savings Account/Flexible Spending Account
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Paid Family Medical Leave and Long-Term Disability Insurance
  • Hospital Indemnity, Critical Illness, Accident, and Identity Theft Protection
  • Pet Insurance

ProMed does not discriminate in employment opportunities or practices on the basis of race, color, creed, religion, national origin, ancestry, age, sex, marital status, order of protection, disability, military status, sexual orientation, gender identity, pregnancy, public assistance, family status, unfavorable discharge from military service, genetic information or other segmenting factor protected by law, or local human rights commission activity.

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