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Associate Director Quality Control Jobs in Rochester, MN

As a Quality Lab Technician, you will be an integral part of the Quality & Food Safety department ... Upon completion of waiting period, associates are eligible for: * Medical and Prescription Drug ...

Quality Technician

Hayfield, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

West Concord, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

Waltham, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

Sargeant, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

Claremont, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

Wanamingo, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

Quality Technician

Dodge Center, MN · On-site

$21 - $25/hr

... • Associates Degree in Science related field • Prior Quality Control/Quality Assurance experience • Prior knowledge of Pet Food manufacturing Considered candidates will receive a phone call ...

REI Lab Director

Rochester, MN · On-site

$107K - $140K/yr

This position is responsible for monitoring quality control, record-keeping, and quality assurance ... An on-site laboratory director is desired.

REI Lab Director

Rochester, MN · On-site

$97K - $127K/yr

This position is responsible for monitoring quality control, record-keeping, and quality assurance ... An on-site laboratory director is desired.

REI Lab Director

Rochester, MN · On-site

$97K - $127K/yr

This position is responsible for monitoring quality control, record-keeping, and quality assurance ... An on-site laboratory director is desired. About Us Why Mayo Clinic Mayo Clinic is top-ranked in ...

This position is responsible for monitoring quality control, record-keeping, and quality assurance ... An on-site laboratory director is desired. Exemption Status Exempt Compensation Detail The minimum ...

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Showing results 1-20

Associate Director Quality Control information

See Rochester, MN salary details

$31.5K

$127.7K

$217K

How much do associate director quality control jobs pay per year?

As of Aug 5, 2026, the average yearly pay for associate director quality control in Rochester, MN is $127,672.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,500.00 and $153,500.00 per year, depending on experience, location, and employer.

What are the main challenges an associate director quality control typically faces when managing a diverse QC team?

An Associate Director of Quality Control often manages teams with varied technical backgrounds, which can lead to challenges in aligning processes, maintaining consistent training standards, and ensuring clear communication across functions. Balancing the demands of regulatory compliance, tight production timelines, and continuous improvement initiatives is also a common challenge. Successful leaders in this role foster a culture of collaboration, prioritize ongoing training, and implement standardized procedures to help their teams deliver reliable results and support broader organizational goals.

What is an associate director quality control?

An Associate Director of Quality Control is a senior management professional responsible for overseeing the quality control processes within an organization, often in industries like pharmaceuticals, biotechnology, or manufacturing. They lead teams that test and monitor product quality, ensure compliance with regulatory standards, and develop strategies to improve testing procedures. Their role involves managing budgets, mentoring staff, and collaborating with other departments to uphold product integrity. Associate Directors of Quality Control often report to higher-level executives and play a key role in maintaining customer trust and regulatory approval.

What are the key skills and qualifications needed to thrive as an associate director quality control?

To thrive as an Associate Director of Quality Control, you need in-depth knowledge of quality management systems, regulatory compliance, and relevant scientific or technical expertise, typically supported by a degree in life sciences or engineering. Familiarity with laboratory information management systems (LIMS), quality assurance software, and certifications such as Six Sigma or ASQ are highly valuable. Leadership, problem-solving, and strong communication skills help drive team performance and foster cross-functional collaboration. These skills ensure rigorous product quality, regulatory adherence, and operational efficiency in quality-driven environments.

What is the difference between Associate Director Quality Control vs Quality Control Manager?

AspectAssociate Director Quality ControlQuality Control Manager
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)
Work EnvironmentLeadership role in labs or manufacturing facilities, overseeing teamsSupervises QC teams, conducts testing, and ensures compliance
Industry UsageUsed in pharmaceutical, biotech, and biotech manufacturing companiesCommon in similar industries, often reporting to Associate Directors

The Associate Director Quality Control typically holds a higher strategic and leadership role, overseeing multiple teams and ensuring compliance at a broader level. The Quality Control Manager focuses more on daily testing, team supervision, and operational tasks. Both roles require similar credentials but differ in scope and responsibility.

What job categories do people searching Associate Director Quality Control jobs in Rochester, MN look for? The top searched job categories for Associate Director Quality Control jobs in Rochester, MN are:
Infographic showing various Associate Director Quality Control job openings in Rochester, MN as of July 2026, with employment types broken down into 1% As Needed, 64% Full Time, 33% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $127,672 per year, or $61.4 per hour.

Associate Director, Facilities - DPF

Vhr_unither

Stewartville, MN

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 hours ago


Job description

California, US residentsclick here.

The job details are as follows:

Who We Are

We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.

United Therapeutics (Nasdaq:UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).

The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.
Who You Are

The Associate Director, Facilities (DPF) owns end-to-end operational leadership and execution for the entire Designated Pathogen Free (DPF) Facilities Maintenance network. This is a network-level role responsible for driving performance across the DPF sites. The Associate Director directly leads the Site Facilities Managers and runs the DPF Facilities Maintenance organization as one unified, high-performance operation with consistent standards, real staffing flexibility, and rapid cross-site support to deliver exceptional reliability and compliance in uptime-critical environments. Reporting to the Director, Maintenance, this position maintains deep operational engagement across all sites, works in close alignment with Site Directors and site leadership, and takes direct ownership of day-to-day results while partnering with Facilities Programs & Operations on enterprise standards and programs. This is not a site-level role. It carries full network accountability for execution outcomes. Success is defined by network reliability, audit readiness, rapid recovery, execution consistency, successful facility startups and expansions, and sustained high performance in a lean multi-site model.

  • Drive overall operational performance, reliability, and execution across the full DPF network, including buildings, infrastructure, utilities, GMP systems, and critical environmental controls
  • Contribute to functional strategic planning and multi-year operational roadmaps for the DPF Facilities Maintenance network in alignment with broader organizational goals
  • Directly lead, develop, coach, and support Site Facilities Managers while maintaining strong alignment and coordination with Site Directors and site leadership at each location
  • Establish, enforce, and continuously improve consistent operational standards, escalation protocols, and staffing models across the DPF network
  • Drive workforce planning, cross-site staffing flexibility, and rapid deployment of resources to support outages, startups, expansions, vacancies, and peak demand
  • Ensure rapid incident response, effective recovery, and permanent corrective actions for critical facilities and GMP systems
  • Lead operational readiness, commissioning, startup, expansion, transition, and renovation activities to the highest standards
  • Oversee vendor and contractor performance with rigorous accountability to quality, SLAs, and operational delivery
  • Support development and management of the DPF network operating budget, including forecasting, expense tracking, and cost optimization initiatives
  • Deliver full GMP/GxP, safety, and regulatory compliance with outstanding audit readiness across the network
  • Maintain regular, extended on-site presence across all DPF sites each month and provide direct operational leadership and hands-on field support during prolonged absences, vacancies, startups, critical incidents, or periods of elevated demand

Minimum Requirements

  • 15+ years progressive leadership experience in facilities, maintenance, engineering, or operations within pharmaceutical, biotech, biologics, or other complex FDA-regulated research and product development environments with a H.S. Diploma/GED or 14+ years progressive leadership experience in facilities, maintenance, engineering, or operations within pharmaceutical, biotech, biologics, or other complex FDA-regulated research and product development environments with an Associate Degree or 12+ years progressive leadership experience in facilities, maintenance, engineering, or operations within pharmaceutical, biotech, biologics, or other complex FDA-regulated research and product development environments with a Bachelor's Degree
  • Proven operational leadership and ability to drive high execution across distributed teams under pressure
  • Strong technical troubleshooting and decisive judgment in regulated GMP environments
  • Track record building staffing flexibility and cross-site collaboration
  • Solid understanding of facilities infrastructure, GMP utilities, maintenance execution, and vendor management
  • Ability to move seamlessly between strategy and hands-on field leadership
  • Ability to interpret, apply, and enforce GMP/GxP regulations and compliance requirements
  • Valid driver's license and willingness to travel extensively (a minimum of 30-40% under normal conditions and will increase during start ups, major outages, or peak periods)

Preferred Qualifications

  • Associate Degree in engineering, facilities/operations management, or related field OR a Bachelor's Degree in engineering, facilities/operations management, or related field
  • 5+ years of demonstrated success operating in lean, flexible, or cross-site operational models within regulated research or product development environments

Job Location

United Therapeutics is open to candidates located within the Eastern or Central Time Zones of the United States, with a strong preference for candidates located near, or willing to relocate near, one of the DPF facilities in Christiansburg, VA; Houston, TX; or Stewartville, MN.

This is a travel-intensive hybrid role that requires monthly on-site leadership presence at all DPF sites. The successful candidate will maintain a primary operating location while providing regular, extended leadership support across the full DPF network. Time spent at each site will vary based on operational priorities, staffing conditions, startup activities, outages, and business needs.

The salary range for this position is $149,000 - $200,000 per year and reflects our good-faith estimate of the compensation for this role at the time of posting. An employee's position within the salary range will be based on factors such as education, qualifications, experience, skills, geographic location, and business needs, as well as other factors permitted by law at the time of posting. This range may be modified in the future based on company and market factors.

At United Therapeutics, our mission and vision are one. We use our enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our other stakeholders. We are bold and unconventional. We have fun, we do good.

Eligible employees may participate in the Company's comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off & paid parental leave benefits, disability benefits, and more. For additional information on Company benefits, please visit https://www.unither.com/careers/benefits-and-amenities

United Therapeutics Corporation is an Equal Opportunity Employer, including veterans and individuals with disabilities.