1

Senior Quality Control Associate Jobs in Rochester, MN

Senior Microbiologist

Rochester, MN · On-site

$80K - $120K/yr

POSITION SUMMARY The Senior Microbiologist provides technical leadership and independently executes microbiological quality control activities that support the manufacture of sterile ...

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

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

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

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 ...

Quality Engineer III

Rochester, MN · On-site

$90K - $114K/yr

Audits process to ensure proper use and corrective action when out-of-control limit is reached. • ... senior engineers. • Ensures that records/files are initiated and maintained in all relevant ...

Senior Mechanical Engineer

Rochester, MN · Hybrid

$102K - $134K/yr

Senior Mechanical Engineer - Bloomington or Rochester, MN (Hybrid) SIGN-ON BONUS up to $10K The ... Perform QA/QC of design work * Oversee and provide guidance to junior engineers * Lead project ...

Senior Mechanical Engineer

Rochester, MN · On-site

$102K - $134K/yr

Senior Mechanical Engineer - Bloomington or Rochester, MN (Hybrid) SIGN-ON BONUS up to $10K The ... Perform QA/QC of design work * Oversee and provide guidance to junior engineers * Lead project ...

Caribou Associate-PT

Zumbrota, MN · On-site

$11.50 - $13/hr

In addition to serving our customers their desired coffee, you'll be trained in observation of dates, quality control for freshness, rotating goods, refilling product, cleaning fresh food storage ...

New

next page

Showing results 1-20

Senior Quality Control Associate information

See Rochester, MN salary details

$11

$25

$38

How much do senior quality control associate jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for senior quality control associate in Rochester, MN is $25.88, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $31.54 per hour, depending on experience, location, and employer.

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

To thrive as a Senior Quality Control Associate, you need a strong background in analytical testing, quality assurance principles, and relevant scientific education, often with a bachelor’s degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and regulatory compliance requirements is typically expected, along with proficiency in using laboratory instruments. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for excelling in this role. These competencies ensure the reliability of product quality, support regulatory compliance, and contribute to efficient cross-functional collaboration within the organization.

What are some typical challenges senior quality control associates face when overseeing multiple projects simultaneously?

Senior Quality Control Associates often manage several projects at once, which can present challenges such as balancing competing deadlines, ensuring consistent application of quality standards, and effectively communicating with cross-functional teams. Staying organized and prioritizing tasks is essential to prevent bottlenecks and maintain high-quality deliverables. Additionally, adapting quickly to changes in project scope or regulatory requirements is a key part of the role, as is mentoring junior team members to uphold best practices.

What is the difference between Senior Quality Control Associate vs Quality Control Associate?

AspectSenior Quality Control AssociateQuality Control Associate
Required CredentialsBachelor's degree, relevant certifications (e.g., CQE)Bachelor's degree often preferred, certifications optional
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or production settings
Employer & Industry UsagePharmaceuticals, biotech, manufacturing companiesPharmaceuticals, biotech, manufacturing companies
Job ResponsibilitiesOversees testing, reviews quality data, mentors junior staffPerforms testing, documents results, supports quality checks

The main difference between a Senior Quality Control Associate and a Quality Control Associate lies in experience, responsibilities, and leadership. Senior roles typically involve overseeing testing processes, mentoring staff, and ensuring compliance, while associate roles focus on executing tests and documenting results. Both positions are vital in maintaining product quality in industries like pharmaceuticals and manufacturing.

What does a senior quality control associate do?

A Senior Quality Control Associate is responsible for overseeing and performing quality control tests on products or materials to ensure they meet company and regulatory standards. They analyze test data, identify trends or deviations, and help implement corrective actions when issues are found. Additionally, they may mentor junior team members, assist in developing testing protocols, and collaborate with other departments to resolve quality concerns. Their work is essential in maintaining product consistency, safety, and compliance within the organization.

Senior Quality Analyst - FDA Regulated Manufacturing

Mayo Clinic

Rochester, MN • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 13 days ago


Mayo Clinic rating

7.8

Company rating: 7.8 out of 10

Based on 693 frontline employees who took The Breakroom Quiz

132nd of 887 rated healthcare providers


Job description


The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work to identify and reduce regulatory, accreditation, and compliance risk by continuous monitoring and evaluating current facility policies and practices to ensure compliance is built into the operational systems. Oversees manufacturing compliance by making interpretations and developing executive summaries of regulatory and compliance information, maintaining registration information, communication with external regulatory and accreditation agencies. The Sr. Quality Analyst communicates and works effectively with leadership to take necessary actions to mitigate identified risks; Is accountable for the effective implementation of the Quality Management System (QMS); and serves as the subject matter expert on the policies, processes and procedures of the QMS by developing a broad knowledge of the practice, business and technology as it relates to product manufacturing.
Qualifications
A master's degree in product manufacturing medicine, business, regulatory compliance, or management and 5 years' experience in a quality related field is preferred or a bachelor's degree and 5 years' experience supporting FDA regulated product manufacturing, quality, regulatory, or compliance. Knowledge and experience in the application of laws, regulations, and guidance documents related to FDA regulated industries (biologics, pharmaceuticals, etc.) and previous experience with FDA GMPs, EU regulations, and/or ISO certification for product manufacturing is required. Demonstrated ability to interpret regulations and translate them into compliant, inspection-ready operational practices is highly desired. Exceptional human relations and communication (written, verbal, and listening) skills are required. Organizational project management skills are essential, along with analytical and critical thinking skills. Must be flexible and capable of adapting to and facilitating change. Should be very detail-oriented and have the ability to work independently and productively with minimal direction and routinely exercise initiative and sound judgment. Must have the ability to lead, motivate, and influence others. Compliance issues may create difficult situations for the individuals involved; therefore, objectivity and professionalism is essential. Must be experienced in conducting audits. Remains abreast of current, new, and developing industry trends, regulations, and legal positions related to FDA regulated manufacturing, patient care, and information management. Possesses strong human relations skills and problem-solving skills in order to influence all levels of the organization toward regulatory and accreditation compliance. Possesses strong written and verbal communication skills. Works independently with minimal direction and is self-motivated.
Must have demonstrated capacity to comprehend complex protocols, programs, and situations. The ability to exercise good judgment in ambiguous situations while under pressure and tight deadlines, and strong coping skills are required. Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities. Must also be flexible with work schedule as needed to meet customer needs. Experience working in a research environment is preferred. Must be self-motivated and able to independently schedule workday activities with minimal direction. ASQ certification in quality and/or GMP principles (e.g., quality process analyst, quality improvement associate, etc.) is strongly encouraged.
About Us
Why Mayo Clinic
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.
Benefits Highlights
  • Medical: Multiple plan options.
  • Dental: Delta Dental or reimbursement account for flexible coverage.
  • Vision: Affordable plan with national network.
  • Pre-Tax Savings: HSA and FSAs for eligible expenses.
  • Retirement: Competitive retirement package to secure your future.

About the Team
Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is.
Equal Opportunity
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law". Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization.

What Mayo Clinic employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Mayo Clinic logo

About Mayo Clinic

Sourced by ZipRecruiter

Mayo Clinic is the largest integrated, not-for-profit medical group practice in the world. We're building the future, one where the best possible care is available to everyone — and more people can heal at home. Our relentless research turns into earlier diagnoses and new cures. That's how we inspire hope in those who need it most. At Mayo Clinic, experts work together to solve the most challenging unmet needs of patients. Our history of innovation dates back almost 150 years, when brothers Will and Charlie Mayo pioneered an integrated, team-based approach to medicine. Today, that trailblazing spirit drives innovations like Mayo Clinic Platform — which powers new technologies to change how care is delivered to all.

Industry

Hospitals

Company size

10,000+ Employees

Headquarters location

Rochester, MN, US

Year founded

1919