11 Garment Sorter jobs in Eagan

**Title:** Quality Control Technician
**Location:** St. Paul, MN (100% Onsite)
**Duration:** 6 Months
**Pay Range :** $25/hr to $28/hr (On W2)
We are looking for a " **Quality Control Technician** " to join one of our Fortune 500 clients.
**Job Responsibilities:**
+ Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
+ Perform a wide variety of activities to support the Quality Management System.
+ Review finished goods batch records.
+ Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
+ Maintain an organized workspace
+ Scan and file records in electronic documentation system, cabinets and into an electronic record database.
+ May assist in supporting the Document Control program, record retention areas, and sample retention areas
+ Ability to work in a controlled cleanroom environment and ensure proper gowning.
+ Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)
**Education:**
+ Experience 2-5 years in quality assurance role in medical device industry is preferred.
**Other Skills and Abilities:**
+ Ability to follow procedures and accurately document results
+ Understanding the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
+ Attention to detail.
+ Strong organizational skills
**We are looking for the candidate who are eligible to work with any employers without sponsorship** .
If you're interested, please click **"Apply"** button
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

Quality Control Inspector

Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.

The Quality Control Inspection team plays a key role supporting our manufacturing operations at the Maple Grove site. This role is involved in a wide range of inspection tasks, where the primary goal is to assure that the products we produce are conforming to specifications and properly evaluated for compliance to visual, dimensional, functional, and various other specified requirements.

The QC Inspector will be responsible for performing inspections in a highly regulated medical device development and manufacturing environment across all areas of standard work for the team (receiving inspection, first article inspections, label verifications, valve inspections, tissue inspections, pre-sterile product inspections, and sterile product inspections). This is a high visibility role with daily interactions across a wide range of peer groups in the Maple Grove site.

Shift: Day Shift, Monday through Friday, 6:00 a.m. - 2:00 p.m.

At Anteris Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions.

Primary Duties and Responsibilities

Perform all duties listed below in strict compliance with the Anteris Quality Management System including Good Documentation Practices.

• Perform receiving inspection on material/products supplied to Anteris to ensure conformance to requirements and specifications.
• Perform microscope and other aided visual inspections on biological tissue based medical device products to ensure conformance to processing requirements and specifications.
• Perform machine/software-controlled inspections on products to ensure conformance to processing requirements and specifications.
• Perform inspections, as required by procedure, in support of first article inspections and label verifications.
• Perform physical and visual inspections on material, products, and/or packaging being processed for sterilization.
• Make an informed decision, based on training to tasks assigned, on the acceptance of materials, products, and inspected features, requirements, and specifications in all standard work tasks.
• Complete and maintain accurate records of inspection activities, including measurements, observations, results, conclusions, nonconformance issues, and full completion of quality record fields in support of standard work tasks.
• Collaborate with peers in Operations to effectively stay on plan, be mutually organized to goals, and communicate effectively through escalation channels as required.
• Other tasks assigned by group lead or designee.

Skills, Knowledge, Experience & Qualifications

Required Skills and Knowledge:

• High School diploma or equivalent.
• 4+ years' overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment.
• 2+ years' equivalent work experience directly applicable to Primary Duties and Responsibilities listed above.
• Strong attention to detail and experience in reading, interpreting, and comprehending product requirement documents and specifications.
• Experience in learning and cross-training on widening set of responsibilities in a team-based environment.
• Experience working directly with computers to input data, perform electronic based work tasks, complete training, and manage email communications.
• Effective verbal and written communication.
• Ability to work in a fast-paced environment.
• Effective problem-solving and troubleshooting skills.

Preferred Skills and Knowledge:

• Vocational or technical training in assembly, sewing, or inspection of biological tissue based medical devices.
• Vocational or technical training in the use of microscopes, including the use of specialized reticles and/or tappi charts.
• Vocational or technical training in the use of MicroVu optical inspection systems.
• Vocational or technical training in Lean or 5S principles.
• Vocational or technical training in GD&T principles and specification designs.

What We Offer:

• Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
• Collaborative and dynamic work environment with a culture of innovation and excellence.
• Competitive compensation package, including salary, performance-based bonuses, and stock options.
• Career development opportunities and a chance to be part of a growing company that values its employees.

Health and Wellness Offerings:

• Medical, Dental, and Vision Plans
• Flexible Spending Account (FSA)
• 401k + Company Match
• Life, AD&D, Short Term and Long-Term Disability Insurance
• Bonus Plan Eligibility
• Employee Equity Program
• Paid Holidays & PTO
• Employee Assistance Program
• Inclusive Team Environment

Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations.

Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.

**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:
$40,300.00 - $66,250.00
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:
+ Run QC assays for reagents and consumables.
+ Precise and meticulous observation and recording of all details of QC assay, which are not limited to but including: lot numbers, and physical observations of materials
+ Keep a clean and organized workspace
+ Maintain inventory of reagents and consumables needed to perform QC assays
+ Participate in continuous process improvements efforts
+ Understand and follow appropriate lab protocols
+ Chemical handling and hazards
+ Labeling
+ Safety procedures
+ Department specific SOP's
+ Proper use and maintaining equipment
+ Follow guidelines and comply with all company safety, quality, and training procedures and regulations
+ Perform additional duties as assigned
Education and Experience:
+ Bachelor's degree in Biology, Chemistry, or Engineering with laboratory experience.
+ Associates degree or non- scientific bachelor's with 2+ years' relevant experience working in a quality position for a GMP or life science related industry.
Knowledge, Skills and Abilities:
+ Ability to pipette and maintain records with a high degree of accuracy
+ Work independently with minimal supervision on routine tasks
+ Experience with MS Word, MS PowerPoint, MS Outlook
+ Flexibility to work on multiple tasks with increased effectiveness
+ Strong organizational skills with an attention to detail and quality
+ Ability to support and help others in the team
+ Manages time well and will put in extended time as needed
+ Understanding of basic statistical principles
**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.**
Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.
Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**Description**
**Who is USP?**
The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a hands-on position that supports the important work of USP's microbiology operations team within the microbiology business unit. The incumbent will work independently, with some oversight, and will be primarily responsible for quality control (QC) tasks related to the production of microbial Analytical Reference Materials (ARMs) and reference standards. The incumbent anticipates and solves problems and issues within his/her area of responsibility.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Quality Control Microbiologist has the following responsibilities:
+ Lead quality control microbiology testing at the USP St. Paul, MN site.
+ Perform microbial culture assays on solid agar media.
+ Perform serial dilutions of microbial suspensions.
+ Perform incubation and enumeration of microbial samples on solid culture media.
+ Support operations product release testing of USP Analytical Reference Materials.
+ Coordinate microbial identity testing (DNA sequencing and MALDI-TOF) with external microbiology test lab.
+ Manage and lead product stability testing for USP Analytical Reference Materials.
+ Support R&D testing for new product introductions.
+ Interpret data, identify trends, and report findings to relevant personnel.
+ Ensure equipment is properly calibrated, maintained, and operated according to SOP's and test methods.
+ Contribute to the development and refinement of quality control test methods, procedures, and related SOP's.
+ Adherence to relevant regulatory guidelines where applicable such as Good Manufacturing Practices (GMP), Good laboratory Practices (GLP), and International Organization for Standardization (ISO).
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ Bachelor's degree in a science field and a minimum of 2 years of relevant quality control experience in a pharmaceutical or other regulated industry.
+ Minimum of 2 years of relavent microbiology experience.
+ Proficient in excel, word, power point software applications.
**Additional Desired Preferences**
+ Experience related to microbiology or biological science.
+ Quality control testing experience.
+ Advanced understanding of ISO 9001/ ISO 17034, and ISO 17025.
+ Knowledge of use of USP Compendia (Monographs, General Chapters).
+ Knowledge of FDA regulations, other Compendia, and ICH guidelines.
+ Ability to listen, interpret and influence without direct authority in a cooperative and friendly manner.
+ Detail oriented with well-developed organizational and prioritization skills.
+ Results and timeline driven with demonstrated successful outcomes.
+ Ability to handle multiple priorities and shift priorities as a result of a fast-paced environment.
+ Excellent written and verbal communications skills.
+ Well-developed presentation skills.
+ Demonstrated excellent verbal and written communication skills.
+ Ability to explain complex information simply to a diverse audience.
+ Experience on research and development, instrumentation techniques and analytical skills.
**Supervisory Responsibilities**
None, this is an individual contributor role.
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
**Compensation**
Base Salary Range: USD $74,000.00 - $94,000.00 annually.
Target Annual Bonus: % Varies based on level of role.
Individual compensation packages are based on various factors unique to each candidate's skill set, experience, qualifications, equity, and other job-related reasons.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights ( notice from the Department of Labor.
**Job Category** Laboratory/Production
**Job Type** Full-Time

**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
This position is primarily responsible for performing immunoassay quality control testing to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. These immunoassay products include Quantikine, DuoSet, Luminex, IVD kits, and related product lines.
ESSENTIAL FUNCTIONS
+ Perform ELISA assays according to procedures in order to check in-process and final product for quality performance.
+ Reduce and evaluate data from assays; record data on proper documents.
+ Assist in transfer of new products & technologies from development including attending project meetings, performing assays, and evaluating results.
+ Calibrate equipment according to schedule and keep updated records of calibrations.
+ Formulate reagents needed for testing according to existing SOP documents.
+ Maintain and enter assay data into assay databases.
+ Review assay information and exercise judgement (within defined procedures and practices) to determine appropriate action.
+ Assist in validations by organizing materials, performing assays, and keeping data records.
+ Perform troubleshooting activities under supervision.
+ Assist in implementing change control. Write and/or revise standard operating procedures as needed.
+ Train other team members as needed.
+ Compile reports and present data with proposed action plan under supervision.
+ Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job.
+ Perform additional duties as assigned.
JOB SPECIFICATIONS
**Education and Experience:**
+ Requires a Bachelor of Science degree in Biology, Chemistry, Biochemistry, or related field with 2+ years of related experience, or a Master's degree with up to 2 years related experience.
+ Experience in clinical laboratory or quality control systems with a thorough knowledge of good manufacturing practices is preferred.
**Knowledge, Skills, and Abilities:**
+ Working knowledge of Microsoft Word and Excel is required including computer entry and typing skills
+ Must be able to work in a fast-faced environment where you will be required to follow written SOPs, plan, multi-task, and prioritize your own work to meet various deadlines in an efficient manner
+ Must be able to analyze data in order to make effective decisions
+ Must have good verbal and written communication skills, especially across different groups and sites
+ Must have strong organizational skills, attention to detail, and high level of accuracy
+ Must work well independently and in a team environment including having the ability to collaborate across different groups
+ Must demonstrate strong technical knowledge including knowledge of lab techniques, lab equipment, computer software, immunoassays, and safety practices
+ Flexibility to work alternate or additional hours as needed
**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.**
Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.
Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**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:
$62,300.00 - $102,350.00
This position is primarily responsible for performing immunoassay quality control testing to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. These immunoassay products include Quantikine, DuoSet, Luminex, IVD kits, Simple Plex, and related product lines.
Within this job function, the Senior Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department and/or within the company. This position would have a focus on managing large-scale databases for immunoassays especially for the Luminex product line.
ESSENTIAL FUNCTIONS
§ Perform immunoassays according to procedures to evaluate in-process and final products for quality performance.
§ Reduce and evaluate data from assays; record data on proper documents. Maintain and enter data into assay databases. Create large-scale databases for data trending and historical analysis.
§ Review assay information for in-process product approval and exercise judgement (within defined procedures and practices) to determine appropriate action.
§ Have strong immunoassay knowledge and solid troubleshooting skills to independently identify root causes of issues.
§ Find process improvements in daily routines to improve product quality and/or process efficiency with a focus on data analysis efficiency for the Luminex product line.
§ Assist in transfer of new products & technologies from development including attending project meetings, performing assays, and evaluating results.
§ Calibrate equipment according to schedule and keep updated records of calibrations.
§ Formulate reagents needed for testing according to existing SOP documents.
§ Write test method validation plans and reports. Assist in validations by organizing materials, performing assays, and keeping data records.
§ Write and revise standard operating procedures, including instrument maintenance, qualification and calibration.
§ Collaborate with various departments, including Development, Operations, Process Engineering, and Quality Assurance (QA) to ensure the performance of products. Perform troubleshooting testing as required and assist in writing and implementing change control.
§ Be a leader in the lab helping develop other team members.
§ Be self-sufficient at compiling reports and presenting data with proposed action plan.
§ Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job.
§ Perform additional duties as assigned.
JOB SPECIFICATIONS
Education and Experience:
§ Requires a Bachelor of Science degree in Biology, Chemistry, Biochemistry, or related field with 5+ years of related experience, or a Master's degree with 2+ years related experience.
§ Experience in clinical laboratory or quality control systems with a thorough knowledge of good manufacturing practices is preferred.
§ Experience with creating and maintaining macros as well as database management. Experience with programs like Python and VBA to analyze large data sets is desirable.
Knowledge, Skills, and Abilities:
· Working knowledge of Microsoft Word and Excel is required
· Must be able to work in a fast-faced environment where you will be required to follow written SOPs, plan, multi-task, and prioritize your own work to meet various deadlines in an efficient manner
· Must be able to analyze data in order to make effective decisions
· Must have good verbal and written communication skills, especially across different groups and sites
· Must have strong organizational skills, attention to detail, and high level of accuracy
· Must work well independently and in a team environment
· Must demonstrate strong technical knowledge including knowledge of lab techniques, lab equipment, computer software, immunoassays, and safety practices
· Flexibility to work alternate or additional hours as needed
Job Demands and Conditions Analysis:
Provide details on the physical demands and work environment that are job related and consistent with business necessity. Documenting the physical demands and work environment conditions in a job description will ensure ADA compliance. Be certain to list all items that are required to perform the job effectively. Use the chart below to clarify how much on-the-job time is spent on each item listed.
**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.**
Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.
Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**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:
This position is primarily responsible for performing immunoassay quality control testing to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. These immunoassay products include Quantikine, DuoSet, Luminex, IVD kits, and related product lines.
ESSENTIAL FUNCTIONS
§ Perform ELISA assays according to procedures in order to check in-process and final product for quality performance.
§ Reduce and evaluate data from assays; record data on proper documents.
§ Assist in transfer of new products & technologies from development including attending project meetings, performing assays, and evaluating results.
§ Calibrate equipment according to schedule and keep updated records of calibrations.
§ Formulate reagents needed for testing according to existing SOP documents.
§ Maintain and enter assay data into assay databases.
§ Review assay information and exercise judgement (within defined procedures and practices) to determine appropriate action.
§ Assist in validations by organizing materials, performing assays, and keeping data records.
§ Perform troubleshooting activities under supervision.
§ Assist in implementing change control. Write and/or revise standard operating procedures as needed.
§ Train other team members as needed.
§ Compile reports and present data with proposed action plan under supervision.
§ Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job.
§ Perform additional duties as assigned.
JOB SPECIFICATIONS
Education and Experience:
§ Requires a Bachelor of Science degree in Biology, Chemistry, Biochemistry, or related field with 2+ years of related experience, or a Master's degree with up to 2 years related experience.
§ Experience in clinical laboratory or quality control systems with a thorough knowledge of good manufacturing practices is preferred.
Knowledge, Skills, and Abilities:
· Working knowledge of Microsoft Word and Excel is required including computer entry and typing skills
· Must be able to work in a fast-faced environment where you will be required to follow written SOPs, plan, multi-task, and prioritize your own work to meet various deadlines in an efficient manner
· Must be able to analyze data in order to make effective decisions
· Must have good verbal and written communication skills, especially across different groups and sites
· Must have strong organizational skills, attention to detail, and high level of accuracy
· Must work well independently and in a team environment including having the ability to collaborate across different groups
· Must demonstrate strong technical knowledge including knowledge of lab techniques, lab equipment, computer software, immunoassays, and safety practices
· Flexibility to work alternate or additional hours as needed
**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.**
Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.
Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

The **Branch Quality Control Analyst** is responsible for performing independent, quality control reviews of retail branch locations to identify operational and compliance risk within the retail branch. This associate works closely with the Compliance and Oversight Program Manager and reports to the Director of Compliance & Oversight for Consumer Banking.
The Compliance & Oversight team is comprised of a group of associates that are very hard working and are passionate about protecting the bank while providing support to our branches. At UMB, we want to be everything to our clients and the Compliance and Oversight Specialist team does just that by ensuring UMB's consumer operations function seamlessly and in a way that protects our client's financial needs.
**_How you'll spend your time:_**
+ Ensuring each review includes, at a minimum: an assessment of branch documentation, certification of cash on hand at the branch, observation of associate behavior and interviews with branch associates to assess the associate's understanding of applicable regulatory requirements.
+ Issuing a summary memorandum of each retail branch quality control review performed, including an overall risk rating articulating the level of risk observed in the branch review.
+ Maintaining an ongoing risk rating guide accurately depicting the amount of risk within each retail branch.
+ Assisting in operations related projects, as needed.
+ Cultivate working partnerships with the Consumer Operations teammates and the Consumer Delivery Team.
+ Collaborate with partners and support Consumer Banking to respond to requests from and timely resolve issues identified by regulatory bodies, internal audits or compliance engagements, or self-assessments.
+ Evaluate operational documentation for monthly operational reporting of branch performance.
+ Act as a supportive resource regarding Consumer Banking operations matters.
+ Support Director of Compliance & Oversight in the aggregation and communication of Compliance & Oversight activities including data aggregation, analysis, and reporting.
**_We're excited to talk with you if:_**
+ 5-7 years of branch / bank operations experience.
+ High school diploma or equivalent.
+ Must live within a major metropolitan area of the UMB footprint.
+ Have the ability to work independently with minimal supervision.
+ Have the ability to build relationships and inspire trust across the organization.
+ Have the ability to present and convey information in a way that is easily understandable to associates at varying levels within the organization.
+ Have the proficient writing ability and strong experience with Microsoft Suite software and related banking applications.
+ Ability to travel up to 75% of a scheduled work week.
**Compensation Range:**
$44,790.00 - $86,510.00
_The posted compensation range on this listing represents UMB's standard for this role, but the actual compensation may vary by geographic location, experience level, and other job-related factors. In addition, this range does not encompass the full earning potential for this role. Please see the description of benefits included with this job posting for additional information._
UMB offers competitive and varied benefits to eligible associates, such as Paid Time Off; a 401(k) matching program; annual incentive pay; paid holidays; a comprehensive company sponsored benefit plan including medical, dental, vision, and other insurance coverage; health savings, flexible spending, and dependent care accounts; adoption assistance; an employee assistance program; fitness reimbursement; tuition reimbursement; an associate wellbeing program; an associate emergency fund; and various associate banking benefits. Benefit offerings and eligibility requirements vary.
**Are you ready to be part of something more?**
You're more than a means to an end-a way to help us meet the bottom line. UMB isn't comprised of workers, but of people who care about their work, one another, and their community. Expect more than the status quo. At UMB, you can expect more heart. You'll be valued for exactly who you are and encouraged to support causes you care about. Expect more trust. We want you to do the right thing, no matter what. And, expect more opportunities. UMBers are known for having multiple careers here and having their voices heard.
_UMB and its affiliates are committed to inclusion and diversity and provide employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex (including gender, pregnancy, sexual orientation, and gender identity), national origin, age, disability, military service, veteran status, genetic information, or any other status protected by applicable federal, state, or local law. If you need accommodation for any part of the employment process because of a disability, please send an e-mail to_ _to let us know the nature of your request._
_If you are a California resident, please visit our_ Privacy Notice for California Job Candidates ( _to understand how we collect and use your personal information when you apply for employment with UMB._
**_Who we are_**
We are more than a company. We are advisors, consultants, problem solvers, friends, community members, experts, and we are here to help you make the best of every moment with a financial foundation that can help you succeed.
Learn more about UMB's vision ( out the road to a career at UMB