Top 10 quality control associate Jobs in minneapolis, mn

Advanced Research Associate - ProteinSimple QC
Bio-Techne —Minneapolis, MN
- $49,700 - $81,650 a year
- Full-time
- Writing skills
- Research
- Mid-level
- Paid parental leave
- Health savings account
Warehouse and Quality Control Associate
Minnesota Tile & Stone LLC —Minnetonka, MN
- $25 - $33 an hour
- Overtime
- Computer literacy
- Basic math
- English
- Health savings account
- Health insurance
Quick Apply
10d
Delivery Driver / Quality Control Associate - Pharmacy
Cardinal Health —Roseville, MN
- $21.50 an hour
- Overtime
- 18 years or older
- Clean driving record
- Customer service
- Paid parental leave
- Health savings account
Senior Research Associate - ProteinSimple QC
Bio-Techne —Minneapolis, MN
- $62,300 - $102,350 a year
- Full-time
- Windows
- 3 years
- Analysis skills
- Paid parental leave
- Health savings account
Shipping & Quality Control Associate
Pacificolor —Plymouth, MN
- $18 - $21 an hour
- Full-time
- Computer literacy
- English
- Forklift
- Health savings account
- Health insurance
Quick Apply
8d
Production Associate (Quality Inspector - 1st & 2nd Shift)
SUPER RADIATOR COILS LIMITED PARTNERSHIP —Chaska, MN
- $22.01 an hour
- Full-time
- Addiction Medicine
- Computer literacy
- Writing skills
- Paid holidays
- Disability insurance

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Advanced Research Associate - ProteinSimple QC

Bio-Techne -
Minneapolis, MN

Apply Now

Job Details

Full-time
$49,700 - $81,650 a year

Benefits

Paid parental leave
Health savings account
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
Benefits from day one
Life insurance

Qualifications

Laboratory project records management
Raw material quality management
Records maintenance
Immunological assays
Quality control product testing
ISO standards
Immunological laboratory techniques
Spreadsheets
Writing skills
Efficiency improvement
Protein analysis (analytical chemistry specialty)
Production deviation management
Corrective and preventive actions (CAPA)
Research
Mid-level
Windows
Data summary reports
Master's degree
Implementing laboratory quality control protocols
Manufacturing standard operating procedures
Analysis skills
Laboratory reports
Biochemical laboratory techniques
Policy & process development
Bachelor’s degree in engineering
Quality control data analysis
Data management
Quality assurance standard operating procedures
Task prioritization
Team training

Full Job Description

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

$49,700.00 - $81,650.00

Position Summary:

Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern . This position is responsible for planning, executing, and managing activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure that all applicable objectives are met, and the product functions as expected. To be successful in this role candidate needs to be skilled in analytical techniques for analysis of biological assays. This position interfaces with Manufacturing, Process Engineering, Product Support, Assay Development and Quality Assurance.

Key Responsibilities:

Compile, document, interpret and manage data from ProteinSimple capillary electrophoresis systems, including iCE and Simple Western platforms, to evaluate the quality of in-process materials and finished goods to either confirm compliance with established quality standards or identify deviations. This includes functional, assay performance, precision, and accuracy testing. Data management comprises analysis and disposition of data produced and curation of that data into established systems.

Ensure that the final product satisfies the product requirements and meet end-user expectations

Revise SOPs of moderate complexity

Initiate and support deviation and out-of-specification investigations

Provide recommendations for corrective actions for low complexity problems and processes

Spot areas for improvement to enhance the QC testing and process efficiency

Maintain clear and accurate records

Attend cross-functional team meeting and present data summaries

Perform lab work when needed, including preparation of controls and reagents, and performing instrument runs

Suppor t projects and new product launch activities of moderate scope that require data review , and contribute to basic project deliverables

May participate in method validations, establishing specifications and writing standard operating procedures

Train team members within the department

Support other QC operations, as needed

Education and Experience:

Bachelor’s degree in B iology , C hemistry , Engineering or similar science degree with 2+ years’ experience.

Master’s degree in B iology , C hemistry , E ngineering, or similar relevant experience

Knowledge, Skills and Abilities:

Knowledge of basic laboratory equipment and skills such as micropipetting , electrophoresis, isoelectric focusing, western blotting, QC functions , test procedures .

Ability to apply understanding of electrophoresis techniques and data analysis to technical troubleshooting or project execution

Outstanding analytical skills , particul arly focused in algebraic equations for solving calculations related to evaluating chromatograms

Ability to independently troubleshoot abnormal test results and determine next steps of moderate complexity

Work fully independentl y on routine tasks and other tasks beyond daily expectations

Flexibility to effectively prioritize own work and manage the work o f multiple tasks

Experience working with and evaluating data with Excel and proficient in all Microsoft Windows functions , as well as JMP and GraphPad Prism

Ability to evaluate moderate volumes of data in a short timeframe

Strong understanding of quality system regulations and standards

Experience working within an ISO compliant, or other regulated environment.

Experience developing, reviewing, deploying Standard Work (WI’s, MI’s, SOPs)

Experience present ing assay data and interpretations

Demonstrated ability to deliver quality work, with high work accuracy.

Demonstrated ability to meet project timelines and collaborate with internal team

Organized with exquisite attention to detail

May be on computer monitor and keyboard for long periods of time

Why Join Bio-Techne:

We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Apply Now

Refine Your Search

quality control associate jobs in minneapolis, mn

Advanced Research Associate - ProteinSimple QC

Warehouse and Quality Control Associate

Delivery Driver / Quality Control Associate - Pharmacy

Senior Research Associate - ProteinSimple QC

Shipping & Quality Control Associate

Production Associate (Quality Inspector - 1st & 2nd Shift)

Related jobs to explore

I want to receive the latest job alert for quality control associate in minneapolis, mn

Explore jobs in more locations

We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.

We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.

We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.

We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.

We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.

We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

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