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Senior Quality Control Analyst Jobs in Minnesota

Cypress HCM

Senior Quality Engineer

New Hope, MN · On-site

$91K - $124K/yr

This Sr Quality Engineer is primarily responsible for providing technical support to ensure ... control. * Demonstrated skills related to root-cause analysis, SPS, equipment and process ...

Bora Pharmaceuticals

Analyst QC

Maple Grove, MN · On-site

$52K - $65K/yr

Job Summary The Analyst QC provides analytical and technical support for the analysis of raw materials (drug substances, excipients, in-process materials, and packaging components), stability samples ...

Bora Pharmaceuticals

Analyst QC

Maple Grove, MN · On-site

$52K - $65K/yr

Job Summary The Analyst QC provides analytical and technical support for the analysis of raw materials (drug substances, excipients, in-process materials, and packaging components), stability samples ...

VitalPath

Sr Quality Engineer

Saint Paul, MN · On-site

$84K - $110K/yr

Join VitalPath in Maplewood as a Sr Quality Engineer! About VitalPath VitalPath is a trusted ... control * Demonstrated skills related to rootcause analysis, SPS, equipment and process ...

Stratasys Ltd

Sr Quality Engineer

Eden Prairie, MN · On-site

$100 - $125/hr

Sr Quality Engineer Job ID: 55438 Category: Manufacturing & Operations Stratasys is a world leader ... Basic statistical analysis skills, including Statistical Process Control. * Strong verbal and ...

3M

Senior Quality Engineer

Maplewood, MN

$90K - $122K/yr

Senior Quality Engineer* Collaborate with Innovative 3Mers Around the World Choosing where to start ... Providing statistical insights through control chart analysis, manufacturing and test method ...

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

As of Sep 8, 2026, the average hourly pay for senior quality control analyst in Minnesota is $47.52, according to ZipRecruiter salary data. Most workers in this role earn between $41.44 and $53.22 per hour, depending on experience, location, and employer.

What does a senior quality control analyst do?

A Senior Quality Control Analyst is responsible for overseeing and ensuring the quality of products or processes within a company, typically in industries like pharmaceuticals, manufacturing, or food production. They design and implement testing procedures, analyze data, identify defects or inconsistencies, and ensure compliance with regulatory standards. Additionally, they mentor junior analysts, prepare reports, and collaborate with other departments to improve quality systems. Their expertise helps maintain product integrity and supports continuous improvement initiatives.

What are some common challenges faced by senior quality control analysts, and how are they typically addressed?

Senior Quality Control Analysts often encounter challenges such as managing tight deadlines while maintaining high accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. These challenges are typically addressed through effective collaboration with cross-functional teams, ongoing professional development to stay updated with industry regulations, and implementing robust standard operating procedures. Additionally, strong analytical and communication skills help in swiftly resolving issues and ensuring continuous improvement within the quality control process.

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

To thrive as a Senior Quality Control Analyst, you need expertise in laboratory testing, analytical methods, and a strong understanding of regulatory standards, often supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), chromatography software, and relevant certifications such as GMP training are typically required. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies ensure accurate quality assessments, compliance with regulations, and efficient collaboration across teams to maintain product integrity.

What is the role of a senior quality control analyst?

A senior quality control analyst is responsible for inspecting and testing products or materials to ensure they meet quality standards and regulatory requirements. They analyze data, identify issues, and collaborate with production teams to improve processes, often using tools like laboratory equipment and quality management systems. This role typically requires experience, attention to detail, and knowledge of industry-specific regulations.

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

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

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

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

What job categories do people searching Senior Quality Control Analyst jobs in Minnesota look for?

The top searched job categories for Senior Quality Control Analyst jobs in Minnesota are:

What cities in Minnesota are hiring for Senior Quality Control Analyst jobs?

Cities in Minnesota with the most Senior Quality Control Analyst job openings:

Senior Quality Control Analyst jobs near you
Infographic showing various Senior Quality Control Analyst job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 10% Part Time, 7% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $98,838 per year, or $47.5 per hour.

Quality Control Analyst II

Takeda Pharmaceutical Company Limited

Brooklyn Park, MN • On-site

$25 - $33.50/hr

Full-time

Re-posted 9 days ago

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

70th 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 Description
About the role:
As a Quality Control Analyst II, you will execute and review routine in-process, drug substance, and stability test methods in a timely manner. You will use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS, Charles River Endoscan, and MODA).
This shift will be working from Saturday to Tuesday.
How you will contribute:
  • Maintain lab operations (including cleaning, ordering of supplies, reagent preparation, stocking, waste disposal).
  • Conduct test methods including samples generated for facility monitoring (i.e., Environmental Monitoring and Critical Utilities), in-process, drug substance, and stability.
  • Own and author quality system events (i.e., laboratory investigations, deviations, CAPA's and change controls).
  • Demonstrate a functional and basic theoretical understanding of laboratory operations and Standard Operating Procedures (SOP's).
  • Work within laboratory environment for extended periods of time, conducting facility monitoring (i.e., Environmental Monitoring and Critical Utility Monitoring) and product tests, reviewing data, maintaining laboratory materials and instruments and other laboratory functions as required.
  • Complete all testing, including special project and protocol testing in a timely and appropriate manner.
  • Maintain data integrity and ensure compliance with company SOP's, specifications, and cGMP regulations.
  • Independently exercise judgment within generally defined Quality Control (QC) procedures and practices in selecting methods and techniques to troubleshoot problems and/or formulate solutions.
  • Decisions have moderate impact on future QC processes and procedures that impact batch disposition.
  • Initiate and own laboratory investigations, basic complexity low and medium risk deviations, CAPA's, and change controls of moderate scope within the electronic Quality Management System.
  • Participate in cross-functional teams.
  • Draft studies and investigations of moderate scope and work on problems where the situation or data requires a review of identifiable factors.
  • Author new SOP's and initiate changes to existing procedures.
  • Train new QC Analysts on routine procedures and practices.
  • May be required to work overtime or be assigned to a different shift as needed.
  • Perform equipment maintenance and calibrations as required.
  • Complete mandatory training within required timeframe.
  • Perform other duties as assigned.

What you bring to Takeda:
  • Bachelor's or master's degree in any Life Sciences with relevant laboratory coursework
  • 3-6 years of relevant experience preferred.
  • Previous experience in a regulated environment preferred.
  • Must understand laboratory instrumentation.
  • Must be able to communicate effectively with managers and peers.
  • Must be able to read, write, and converse in English.
  • Must have basic computer skills. General use of word processing, spreadsheets, databases, etc. for the purposes of work execution, training, performance management, and self-service.
  • Good interpersonal skills and able to work effectively and efficiently in a team environment.
  • Knowledge of cGMP manufacturing
  • Knowledge of chemical, biological and/or microbiological safety procedures.
  • Must display eagerness to learn and continuously improve.

Important Considerations:
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:
  • Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
  • Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
  • Work in a cold, wet environment.
  • Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
  • Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
  • Stand or sit -> Must be able to remain in a stationary or standing position for extended periods of time in both office and laboratory environment.
  • Carry weight, lifting - Frequently moves laboratory materials and portable instruments weighing up to 30 pounds.
  • Climb - Occasionally ascends/descends step ladders to reach materials and/or stairs to collect samples.
  • Dexterity/balance - required to gown for cleanroom work, balance and dexterity are required.
  • May be required to participate in an on-call rotation for off-shift coverage or occasionally work off-shift hours to help support a 24-7 manufacturing department.
  • Willingness to travel to various meetings or training, this could include overnight trips.
  • Requires 0-5% travel.
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
#GMSGQ #ZR1 #LI-MA1
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. Hourly Wage Range:
$24.76 - $38.87
The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage 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 hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.
For information about our benefits, please click here.
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.
Locations
Brooklyn Park, MN
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
No

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About Takeda Ventures

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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

Social media

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