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Quality Control Associate Iii Jobs in Minnesota (NOW HIRING)

Fastenal Company

Quality Control

Winona, MN · On-site

$15/hr

Quality Control 2001 Theurer Blvd, Winona, MN 55987 MN100 Distribution Center Part-time Shift(s ... 3,000 servicing locations, each providing tailored local inventory and personal service for our ...

Lakeshirts

Screenprint Quality Control

Detroit Lakes, MN · On-site

$17 - $22/hr

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

Lakeshirts

Screenprint Quality Control

Detroit Lakes, MN · On-site

$17 - $22/hr

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

Lakeshirts

Screenprint Quality Control

Detroit Lakes, MN · On-site

$17 - $22/hr

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

Wells Fargo

Supervisory Control Associate

Minneapolis, MN · On-site

$68K - $104K/yr

Wells Fargo Advisors (WFA) is seeking a Supervisory Control Associate responsible for direct support of branches and their responsibilities for remote compliance supervision of Private Client Group ...

H.B. Fuller

Quality Control Technician

Fridley, MN · On-site

$26 - $28/hr

Day Shift (6am-6:30pm) 2-2-3 Schedule (Includes every other Saturday, Sunday, Monday) Pay: $26.00 ... Associate degree, junior college diploma, or higher education in Chemistry or a related field.

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Quality Control Associate Iii information

What does a Quality Control Associate III do?

A Quality Control Associate III is responsible for performing advanced quality control testing and analysis to ensure products meet established standards and regulatory requirements. They typically oversee and mentor junior team members, review and interpret test results, troubleshoot issues, and help develop or refine quality control procedures. This role often involves working in laboratory settings, documenting findings, and collaborating with production and quality assurance teams to maintain high product quality.

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

To thrive as a Quality Control Associate III, you typically need a strong background in biology, chemistry, or a related field, along with experience in laboratory testing and quality assurance processes. Familiarity with technical tools such as HPLC, GC, LIMS, and compliance with GMP/GLP guidelines, as well as certifications like ASQ, are commonly required. Attention to detail, problem-solving, and effective communication are crucial soft skills for identifying issues and collaborating with cross-functional teams. These skills and qualifications ensure accurate testing, regulatory compliance, and the delivery of high-quality products in regulated industries.

What are some common challenges faced by a Quality Control Associate III, and how can they be addressed?

Quality Control Associate III professionals often encounter challenges such as managing tight deadlines for testing, adapting to evolving regulatory requirements, and troubleshooting unexpected deviations in product quality. Addressing these challenges requires strong organizational skills, a thorough understanding of compliance standards, and proactive communication with cross-functional teams like manufacturing and R&D. Leveraging robust documentation practices and continually updating knowledge through training can also help ensure accuracy and efficiency in quality control processes.

What is the difference between Quality Control Associate Iii vs Quality Control Associate Ii?

AspectQuality Control Associate IiiQuality Control Associate Ii
Required CredentialsTypically requires a bachelor's degree in a related field and relevant certificationsUsually requires an associate degree or equivalent experience, with some certifications preferred
Work EnvironmentLaboratory and manufacturing settings, performing complex testing and analysisSimilar environments but with more routine testing and data collection
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for quality assuranceCommonly found in similar industries, supporting quality control processes

The main difference between Quality Control Associate Iii and Quality Control Associate Ii lies in experience, responsibilities, and required credentials. The Associate Iii typically handles more complex testing, requires higher education or certifications, and may supervise or mentor lower-level associates. The Associate Ii performs routine testing and data collection, supporting overall quality assurance efforts.

What cities in Minnesota are hiring for Quality Control Associate Iii jobs?

Cities in Minnesota with the most Quality Control Associate Iii job openings:

Quality Control Associate Iii jobs near you

Associate Director, Quality Control

Brooklyn Park, MN • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

Title: Associate Director, Quality Control (Onsite) - Brooklyn Park, MNAbout the role

As an Associate Director, Quality Control, provide strategic and operational leadership for QC laboratory functions (analytical chemistry, microbiology, bioanalytical testing, laboratory systems, and laboratory excellence). Ensure timely, compliant, scientifically sound testing of raw materials, intermediates, in-process samples, and finished drug substance, and drive compliance with Takeda's Quality Management System and applicable cGMP/global regulatory expectations.

How will you contribute
  • Lead QC laboratory operations (analytical chemistry, microbiology, bioanalytical).
  • Manage teams supporting routine, in-process, release, stability, and investigative testing.
  • Establish/maintain compliant laboratory processes, procedures, methods, and systems.
  • Serve as QC subject-matter expert for regulatory inspections and audits.
  • Oversee Deviation, CAPA, Change Control, Audit, and Quality Risk Management; perform gap assessments.
  • Lead method transfers, lab expansion, and new product/process introductions.
  • Drive continuous improvement using data analytics, Lean, Six Sigma, DMAIC.
  • Set/track QC performance metrics; manage budgets and staffing/training; delegate and communicate priorities.
What you bring to Takeda
  • Bachelor's degree in life sciences, chemistry, engineering, or related technical discipline (required); Master's/Ph.D. preferred.
  • 10+ years in regulated laboratory operations; experience leading multidisciplinary QC functions.
  • 6+ years management/people leadership (24/7 org experience strongly preferred).
  • Regulatory inspection/audit readiness; Deviation/CAPA, Change Control, Quality Risk Management.
  • Preferred: TrackWise, SAP, Microsoft Office; knowledge of endotoxin and sterility testing.
  • Strong cGMP and Good Data/Documentation Practices; FDA/EMA/PDA and other regulatory requirements.
Other job requirements
  • Work in controlled environments (gowning/PPE); possible clean rooms, multiple shifts/weekends; 5-10% travel.
Benefits (explicitly listed)
  • Medical/dental/vision; 401(k) with match; disability and life insurance; tuition reimbursement; paid volunteer time off/holidays; well-being benefits; up to 80 hours sick time; up to 120 hours paid vacation for new hires.
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