Quality Control Active Cabinet
Quality control analyst job in Minneapolis, MN
Job Description
Quality Control Active Cabinet
OBJECTIVE: Responsible for quality control of Active Cabinets. Ensures cabinets and related components meet company and customer quality standards throughout the entire production process. Ensures electrical safety in the Active Cabinet Test Area is to OSHA and company standards. Develops and documents the Corrective action process utilizing root cause analysis and troubleshooting techniques. Supports the calibration of all test equipment utilized for the Active Cabinet production process.
POSITION RESPONSIBILITIES
Active Cabinet Test
Skilled in interpreting technical drawings, blueprints, and quality specifications to guide and meet project requirements.
Knowledge working with 240V AC and -48V DC power systems to turn up cabinets for test.
Follow process instructions and quality guidelines to complete Functional Test of Active Cabinets.
Supporting internal and external audits to ensure compliance with company, industry standards (e.g., ISO), and relevant safety regulations.
Actively participating in problem-solving activities, root cause analysis, and continuous improvement efforts to address and resolve recurring quality issues.
Utilize various measuring devices to perform routine measurements and tests.
Troubleshoot and correct Test Failures.
Document Test Failures and Train Assembly Technicians on Test Failure modes.
Learn simple coding to develop Functional Test programs/procedures for new Active Cabinets.
Ability to work independently and accept work direction from Manufacturing Engineer Team, Leads, Supervisor and co-workers.
Performs electro-mechanical assembly when needed.
Collaborate with trainers to support the onboarding and retraining of employees to quality standards and procedures.
Assist in building active cabinets when there is no quality testing to conduct.
Quality Focus
Inspects finished cabinets to ensure they comply with quality specifications and technical drawings/blueprints.
Perform tests and use special equipment to ensure package and product quality
Operate all manufacturing equipment efficiently and safely, related to Active Cabinets production
Maintaining detailed and accurate records of all inspections, test results, and quality data. Identifying defects or non-conformances and reporting findings to production teams, supervisors, and management.
Follow process guidelines and expedite quality concerns to management
Demonstrate flexibility and prioritization of work orders
Work with production/maintenance as necessary to support Active Cabinet department
Following Standard of Operations Procedures (SOP's) and WIO's
Inspect, test, or measure materials or products being produced
Utilize correct measuring tools for product build and quality inspections.
Accept or reject finished items according to quality standards and guidelines
Remove all products and materials that fail to meet specifications
Monitor quality standards for all manufactured products
Record the results of inspections through test reports.
Report inspection and test data
Detailed focused to identify flaws and/or deviations from design specifications
Ensure clean work area through good housekeeping practices throughout shift
Assess and verify the accuracy and functional statues of measuring equipment.
Proficiency in quality control and corrective action, non-conforming products, processes, and equipment.
COMPETENCIES:
Initiative: Dealing with situations and issues proactively and persistently, seizing opportunities that arise.
Brings issues to the attention of appropriate personnel as needed
Offers ideas or suggests modified approaches to address current situations or issues.
Undertakes straightforward tasks that go beyond the job's routine demands (e.g., helps others when own work is completed), without being prompted.
Problem Solving: Identifying problems and the solutions to them.
Identifies alternate solutions, considering applicable precedents.
Identifies optimal solutions based on weighing the advantages and disadvantages of alternative approaches.
Evaluates the effectiveness and efficiency of solutions after implementation.
Attention to Detail: Working in a conscientious, consistent and thorough manner.
Seeks out others to check or review own work for accuracy and completeness.
Verifies assumptions and information before accepting them.
Review all relevant information or aspects of a situation before taking action or making a decision.
Teamwork: Working collaboratively with others to achieve organizational goals.
Initiates collaboration with others.
Assumes additional responsibilities to facilitate the achievement of team goals.
Seeking input from other team members on matters that affect them.
POSITION REQUIREMENTS:
Three plus years of Quality Control experience or relevant experience preferred
Five plus years of manufacturing, or light electrical assembly is preferred
Strong attention to detail
Ability to identify colors, and strong eye-hand coordination.
Operating testing instruments preferred
General assembly experience,
Basic electric testing concept
Ability to work with a wide variety of part sizes and weights
Extensive dexterity and hand, wrist, and arm movement
Ability to work in a fast-paced environment.
Ability to read and understand written instructions, basic arithmetic skill and electrical schematics.
Strong communication and problem-solving skills.
Intermediate skill level in both Microsoft Office Suites and computer navigation
Continuous improvement mindset, Lean Sig Sigma training, yellow belt preferred.
Change Management mindset
Safety mindset
Role requires standing or walking for extended periods of time
Able to lift up to 50 lbs.
Forklift Certified, is a plus
BENEFITS for full time:
Comprehensive Medical, Dental, and Vision benefits.
100% company paid Short-term and Long-term disability insurance coverage.
100% company paid Basic Life and Accidental Death and Dismemberment (AD&D) insurance coverage.
100% company paid Business Travel Accident (BTA) insurance.
100% company paid Employee Assistance Program (EAP).
Additional voluntary benefits are offered.
401K plan: Maximum match is 4.5% of the first 6% of contribution.
Employee Stock Purchase Plan:
Clearfield's Time Off Policy includes Personal Time Off (PTO) beginning at three weeks annually. PTO is accrued on the first of the month starting on day of hire. In addition, nine paid holidays per year.
Hourly Salary Range: Starting rate $ 26.00 per hour, Retention Bonus, and Semi-Annual Production Bonus
An Offer of employment will be extended at a level consistent with the experience and qualifications of the candidate. This information reflects the anticipated salary range for this position at the time of posting. The salary range may be modified in the future and actual compensation may vary from the posting based on various factors such as geographic location, work experience, education and/or skill level.
Research & Development (R&D) Technician
Quality control analyst job in Saint Paul, MN
The R&D Technician will support the formulation and development of cosmetic and OTC personal care products, with a focus on skincare and suncare. This role involves preparing and modifying formulations under the guidance of R&D Chemists, performing lab tests, documenting processes, and supporting scale-up activities. The technician must adhere to lab protocols, ensure compliance with regulatory guidelines, and maintain a clean and safe laboratory environment. This position reports directly to the VP of R & D and plays a key role in bringing innovative, high-quality products from concept to launch.
Key Responsibilities:
* Prepare lab batches based on new or modified formulations according to directions from R&D Chemists and Management.
* Assist in formulation adjustments to meet product performance, stability, and regulatory requirements.
* Conduct routine testing of lab batches, including pH, viscosity, specific gravity, appearance, texture, and odor.
* Maintain accurate and organized records of all formulation work, testing data, and observations.
* Ensure all samples and documentation meet internal standards and are archived appropriately.
* Gain familiarity with regulations related to OTC and cosmetic products, including FDA monograph requirements.
* Support scale-up and pilot batching processes, and assist in the transfer of formulas to the production floor as requested by the chemists and R & D management
* Learn and follow proper procedures for weighing, mixing, and batching raw materials in accordance with Good Manufacturing Practices (cGMP).
* Identify and communicate any issues during batching, testing, or stability evaluations to the chemists
* Maintain cleanliness, safety, and organization in the lab environment, including routine maintenance of lab equipment.
* Work on multiple development projects simultaneously and manage shifting priorities as needed.
Requirements
Required Skills/Abilities
* Hands-on experience with laboratory equipment and processes
* Knowledge of safe chemical handling procedures.
* Ability to accurately perform calculations for batching and scaling.
* Strong attention to detail, organizational skills, and commitment to documentation accuracy.
* Effective written and verbal communication skills.
* High level of initiative and problem-solving ability in a fast-paced environment.
* Ability to work both independently and collaboratively as part of a cross-functional team.
* Proficient in Microsoft Office (Excel, Word, Outlook).
* Willingness to learn and adapt quickly to new methods, regulations, and technologies.
Required Education and Experience
* Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related scientific discipline.
Preferred Education and Experience
* Experience working within cosmetic or OTC product environment under FDA regulations (e.g., sunscreens, acne treatments, antiperspirants).
* Familiarity with GMP documentation practices and regulatory compliance requirements.
* Bachelor's degree in Chemistry or Cosmetic Science or advanced training in formulation chemistry.
Quality Control Technician 3
Quality control analyst job in Saint Paul, MN
Job Description
The Quality Control Technician is responsible for laboratory and field testing of materials primarily focusing on asphalt mixes and aggregates. This role is critical to the successful execution of the Airfield Projects and involves frequent travel to job sites across the Pacific and continental U.S and any other location as business dictates. The position requires experience in laboratory procedures, equipment calibration, data integrity, and field test coordination. This individual serves as a key technical contributor within a high-stakes, federally governed infrastructure project.
Essential Duties and Responsibilities
Reasonable accommodations or workable solutions may be made to enable individuals with disabilities to perform essential functions.
• Perform asphalt laboratory testing including extraction, gradation, compaction, and performance assessments in accordance with ASTM, AASHTO, and/or USACE procedures.
• Coordinate daily with project engineers and other technical staff to ensure accurate scheduling, execution, and documentation of test results.
• Operate and maintain laboratory and field testing equipment.
• Produce accurate, legible, and timely testing documentation that supports client reporting and project requirements.
• Contribute to troubleshooting, quality assurance, and process improvement for large-scale material testing programs.
• Represent AET with professionalism and technical integrity while embedded on federal or client job sites.
• Travel frequently and maintain readiness for long-duration field assignments in remote or high-security locations.
• Adhere to all federal, site-specific, and AET safety protocols with a zero-tolerance approach to noncompliance.
Supervisory Responsibility
This position may informally guide or mentor junior technicians on specific assignments but does not include formal supervisory authority.
Qualifications and Education Requirements
Associate degree or higher in Construction Technology, Civil Engineering, Materials Science, or a related field and a minimum of 1 year of direct asphalt laboratory or field testing experience. Or High school diploma or equivalent and a minimum of 3 years of progressive asphalt laboratory or field testing experience.
Must be eligible to work in high-security environments (e.g., military bases) and pass background screening.
Valid driver's license with clean driving record and ability to travel extensively.
Ability to work extended shifts, including nights and weekends, in remote field environments.
Preferred Skills
Airfield Asphalt Lab Technician Certification from NCAT
ACI Aggregate Testing Technician Level I and/or Level II
FAA or Department of Defense project experience.
Strong familiarity with MS-2 Asphalt Institute Asphalt Mix Design Methods/FAA P-401/P-403 mix designs and testing protocols.
Demonstrated ability to work independently in remote locations with minimal supervision.
Experience collaborating with diverse project teams across geographic regions.
Pay Transparency
At AET, we value transparency-from expectations to compensation. This Field Technician role offers a base hourly wage of $28.00 to $34.00, based on skill set and experience. With guaranteed overtime, bonuses, incentives, and travel per diems, total annual compensation can reach up to $146,000.
We provide a comprehensive benefits package that includes health insurance, ESOP, 401(k) with match, life insurance, disability coverage, PTO, and professional development opportunities.
Ideal candidates bring technical field experience, are reliable and safety-focused, and work well in teams. You must be authorized to work in the U.S. without visa sponsorship.
Join AET and be part of a company that values your contributions, supports your growth, and rewards your impact.
Work Environment
This job primarily operates in both laboratory and field environments. The role includes working in temporary field labs, airport job sites, and secure federal locations with tight operational windows and strict compliance oversight.
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands or fingers, handle or feel; and reach with hands and arms. The employee is occasionally required to sit; climb or balance, and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.
AAP/EEO Statement
It is the policy of AET to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.
Method Development Chemist
Quality control analyst job in Minneapolis, MN
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Job Title: Method Development Chemist
Location: Minneapolis, MN
Duration: 3+ months (Possibility of extension)
local candidate needed - Minneapolis, MN.
REQUIRED:
Top 3 must haves:
Chromatography experience
analytical lavatory experience
Seasoned HPLC chemist.
Job Roles & Responsibilities
3 months contract position performing method development on GPC methodology.
Perform and document laboratory work.
Review and approve test records.
Participate in the validation of the new GPC test method
Basic Qualifications and Experience
EDUCATION - Minimum BS in Chemistry or related scientific degrees
EXPERIENCE -
Minimum 1 year in a regulated industry environment with a Bachelor's Degree in Chemistry.
Minimum 3 years of hands on experience operating HPLC
Performing chemistry and/or material properties testing in a high throughput laboratory
Documenting work accurately and completely
Ability to use common software including MS Word, MS Excel, Powerpoint
Self-motivated, able to plan/execute work tasks independently
Critical thinking skills
Safely handle chemical and hazardous materials
Preferred Skills and Experience
Prior experience and knowledge of materials properties and GPC testing
Experience working with laboratory data management system
Experience working with Empower chromatography software
Additional Information
· We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.
Thanks & Regards,
Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # - 732-844-8724
Email id - seema @irionline.com| www.irionline.com
LinkedIn: https://in.linkedin.com/in/seemachawhan
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row
Principal Research and Development Technician
Quality control analyst job in Minnetonka, MN
Working at Freudenberg: We will wow your world!
Responsibilities:
Assist in the development and maintenance of the engineering bill of material (BOM)
Assist in development and implementation of new processes, technologies or tooling needed to build products.
Assist in identifying/developing/qualifying fixture for manufacturing processes.
Assist in the creation and maintenance of tool files.
Support engineering studies and data analysis.
Fabricate or assist in fabrication of units for prototypes and engineering builds.
Assist in setup and performing design verification and process validation.
Assist with drafting and executing protocols within all areas of Product Development such as Design, Process Development and Design Assurance.
Work with engineers to specify, procure and commission equipment and procure material.
Manage product development materials to help maintain traceability and quantities.
Execute inspections of components and devices.
Qualifications:
Associate Degree in a technical area is preferred
Years of experience required depends on level of seniority
Demonstrated mechanical aptitude
Experience performing tedious processes, building prototypes and working with small parts
Basic statistical skills
Basic SolidWorks skills is a plus
Demonstrated ability in Microsoft Word and Excel
Continue to learn and utilize new skills related to typical product development capabilities
Ability to utilize metrology equipment such as calipers, micrometers etc..
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
Freudenberg Medical LLC
Auto-ApplyQuality Control
Quality control analyst job in Minneapolis, MN
Journey Auto Repair is looking to add the right "someone" to our growing team!
You will be playing an essential role in the day-to-day operations with opportunities to learn skills in the Automotive Repair Trade. You are the last line of defense for us to ensure continued, high-quality service and support to our amazing customers. You will be able to help us catch preventative situations and provide a "leave it better than you found it" service before customers pick up their vehicles from our shop. Minor interactions with customers will occur and people will know your name!
You will start as a shop porter/assistant/helper.
Job Duties:
Completion of Quality Control process on Repaired vehicles
Conduct Test Drives Perform Mini-detailing service
Shuttle Customers
Help with shop cleanliness
Other Duties as assigned
Hours and Compensation:
Monday-Friday 7:30am-5:30pm
$14-$18
Job Type: Full-time
Pay: $14.00 - $18.00 per hour
Education:
High school or equivalent (Preferred)
License/Certification:
Driver's License (Required)
Proficient operation of manual and automatic transmission vehicles
Work Location: In person
Job Type: Full-time
Work Location: In person
Quality Systems Associate
Quality control analyst job in Stillwater, MN
Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.
Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist."
Why Join Diasorin?
* Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
* Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.
Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.
Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!
Job Scope
This position is responsible for overseeing, monitoring and enhancing the existing DiaSorin documentation system as well as performing final review and approval of device history records.
Job Tasks and Responsibilities
* Coordinate documentation review and approval cycles through the SmartSolve Document Module
* Ensure good documentation practices are followed across various departments within DiaSorin Inc.
* Prepare and support rapid and deadline driven document delivery for Quality, Compliance and Regulatory inspections as assigned.
* Review and provide guidance on record completion and approve final manufacturing lot documentation.
* Review document change plans to assure compliance with QMS requirements.
* Review for format and prepare release versions of product labeling (IFU, MSDS, Labels).
* Upload and confirm customer facing device labeling (IFU, MSDS) on web portal.
* Coordinate documentation translation.
* Create and maintain part information (bills of material, routings, part numbers etc.) in SAP.
* Provide training and guidance to the organization related to quality system documentation practices.
* Design and develop processes to implement and improve the QMS.
* Maintains and troubleshoots processes and procedures. Helps define QMS requirements
* Maintain records and archive as required per requirements
Education, Experience and Qualifications
* Associate's Degree in Quality, Technical Documentation, Data Analysis or equivalent or equivalent experience required
* Minimum 1+ Years in related field or demonstrated documentation system competence within a cGMP corporate environment required
* Minimum 1+ Years of related documentation system experience within regulated environment required
* Experience using Microsoft Office (MS Word, Excel, PowerPoint) and SharePoint/Teams required
* Good communication skills
* Service oriented mentality and a strong focus on customer needs
* Strong independent / cross-disciplinary skills
* Ability to work independently with minimal supervision as well as with a team
* Ability to work in a regulated environment
* Ability to train team members on basic group procedures and tasks
* Effective process management and analytical skills
The hiring range for this position is $24.30 - $29.70 hourly. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.
Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.
Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation.
The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements.
Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.
Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations.
This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.
Quality Control Inspector I
Quality control analyst job in Osseo, MN
Job DescriptionSalary: $22 - $28 /hr + 10%
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.
Responsible for performing 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.
2+ years overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment.
1+ year's 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 applying to this position, you consent to receive text messages from the Anteris Talent Acquisition team regarding your application. Message and data rates may apply. You may opt out at any time by replying STOP.
Quality Control Chemist
Quality control analyst job in Chaska, MN
The Quality Control Chemist will perform testing and evaluations of raw material, bulk, and finished products in accordance with written procedures. This role requires ensuring current standard operating and test procedures are utilized, maintaining accurate documentation records in compliance with GMP requirements, and developing an understanding of various testing methodologies. The position is crucial in maintaining product quality specifications and customer standards, ensuring test results meet specifications, and performing batch adjustments as needed.
Responsibilities
* Conduct testing and evaluations of raw materials, bulk, and finished products according to written procedures.
* Ensure utilization of current standard operating and test procedures.
* Maintain accurate documentation records in compliance with GMP requirements.
* Develop and maintain understanding of testing methodologies, techniques, and potential errors.
* Ensure product quality specifications and customer standards are met and maintained.
* Perform batch adjustments and troubleshoot out of specification situations.
* Update test procedures and specifications as needed.
* Utilize data to focus improvement efforts to meet customer requirements and regulatory regulations.
* Accurately record all data and pertinent information.
* Document Key Quality Incidents and out of specification situations, determine root cause, and suggest solutions.
* Maintain compliance with regulatory expectations and practices.
* Promote a culture of 'lean action' within the department.
Essential Skills
* Laboratory skills
* Chemistry degree
* 0-6 months of industry experience
* Wet chemistry
* FTIR
* Quality control
Additional Skills & Qualifications
* 4 year degree in chemistry
* 0-2 years of QC industry experience in pharma, cosmetics, or food
* Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus
Work Environment
The Quality Control Chemist will work at the Eden Prairie site, primarily indoors, with exposure to various fragrances. The position requires 12-hour shifts on Friday, Saturday, and Sunday, with potential opportunities to extend to full 40-hour weeks based on workload. Candidates need to be comfortable working independently, as they will be the sole person in the lab but can collaborate with a counterpart at the Chaska facility. The role demands moderate to high physical activity and adaptability to changes in a high-paced work environment. Available shifts include 6pm - 6am (preferred), 7pm - 7am, and 8pm - 8am. Benefits include 2 days of billable accruable vacation, 6 days of billable holiday pay, and billable sick pay.
Pay and Benefits
The pay range for this position is $25.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Chaska,MN.
Application Deadline
This position is anticipated to close on May 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
QUALITY CONTROL TECH. I
Quality control analyst job in Rosemount, MN
Job Description
GENERAL DESCRIPTION
The Quality Control Technician I is responsible for inspecting and testing our products to ensure conformance with PCI standards and design specifications that are detailed on the pour sheet. This position is critical to ensuring the quality and safety of our products.
Salary range ($25.00-27.00). Based on experience.
WHY WORK FOR US?
At Wells, we empower our team members to deliver an exceptional client experience. Our employees are talented problem solvers that shine in preconstruction, engineering, operations, and project management. They bring innovative solutions that yield outstanding results.
In the design and construction industry, we focus on honesty and hard work to build trust that lasts beyond individual projects. Our team is consistently working to improve building processes and raise industry standards. We meet our partners' needs through collaborative efforts that ensure safe and certain results, reducing risks along the way. Together, we help businesses and individuals succeed and change our communities for the better.
WHAT WE HAVE TO OFFER
Wells values our employees and is committed to providing a competitive and comprehensive benefits package.
Please note that the benefits listed here are for
non-union employees. Benefits for union employees are covered under separate collective bargaining agreements which can be obtained through their union business agent or their HR representative.
Health, dental and vision insurance
Paid premiums for short- and long-term disability, and life insurance
Wellness Incentives
Paid holidays
Flex spending for medical and daycare
Health savings account (HSA)
401(k) plan with profit sharing
Access to Nice Healthcare
Employee Assistance Program
Paid Time Off (PTO)
Wishbone Pet Insurance
Critical Illness Benefit Plan
Accident Insurance Plan
Voluntary Hospital Indemnity Plan
Other benefits include Health and Family Care leave for both union and non-union employees.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
Performs pre-pour inspections including dimensions of member, position of reinforcement, location of tensioning strand, and quality of forming.
Post-pour inspection of cast product
Perform wet and hardened required testing on the materials used in the manufacturing of product.
Prepares concrete specimens for testing. Regularly performs test for slump, temperature, unit weight, air content, and cylinder strength.
Involved with tensioning of cable to record elongations and ensure cable is tensioned as designed.
Perform cylinder strength tests to ensure they meet intended strength.
Conduct aggregate gradations and sieve analysis.
Compliance with safety policy and procedures.
Maintains complete Quality Control documentation for inspections and testing performed.
Identify and record quality issues and works with Production to resolve those issues.
Acts in professional manner that demonstrates the individual has good character and can be trusted by all employees.
Complete special projects as requested and performs other duties as assigned.
Willingness to work outside all year long (Location Specific)
EDUCATION, SKILLS, AND ABILITIES REQUIRED
High School Diploma or GED.
Must have interpersonal communication skills to interact with co-workers, supervisors, and managers.
Experience with Microsoft Office.
Must be able to solve problems quickly and efficiently.
General math skills, be able to read a tape measure.
Strong attention to detail and organizational skills.
Knowledge of safety procedures that need to be followed.
Ability to work with others to get the project completed efficiently.
Must be motivated and self driven to complete a task.
Understand and accepts changes that are implemented to become best in Class.
PHYSICAL REQUIREMENTS/ ADA ESSENTIAL FUNCTIONS
Physically able to lift up to 75 lbs, occasionally.
Physically able to push, pull, lift, bend, climb, kneel, twist, squat, crawl and use hands/forearms repetitively and frequently.
Ability to move around for up to 12 hours per day.
Ability to work from ladders, scaffolding, swing stages and man lifts at various heights frequently.
WORKING CONDITIONS
Moderate to high risk of exposure to unusual elements.
Moderate to high risk of safety precautions.
Moderate to high exposure to production environment.
Wet, hot, humid, and wintry conditions (weather related) (plant specific)
Ability to work outside year-round (plant specific)
This position profile identifies the key responsibilities and expectations for performance. It cannot encompass all specific job tasks that an employee may be required to perform. Employees are required to follow any other job-related instructions and perform job-related duties as may be reasonably assigned by his/her supervisor.
“
Equal Opportunity Employer, including Veterans and Individuals with Disabilities
.
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Wells participates in E-Verify and will provide the federal government with your I-9 Form information to confirm you are authorized to work in the U.S.
#INDLABOR
Quality Control Inspector PCB Manufacturing
Quality control analyst job in Osseo, MN
PCB Manufacturing | QC Inspector
Scope:
Inspect and evaluate final products to ensure compliance to customer requirements prior to delivery.
Essential Job Function:
Be able to complete AS 9102 Reports
Perform Final Inspection on finished product to ensure compliance to customer requirements.
Read customer drawings
Perform measurements with measurement tools such as calipers, micrometers, and pin gages.
Perform rework as appropriate, which may include mask touch-up, material removal with an x-acto knife, burnishing, soldering irons, final finish brush plating, sanding
Verify acceptability of rework after completion
Identify and mark non-conforming product to ensure it is not delivered
Prepare standard and AS9102 First Article Reports as needed
Verify certifications and reports are complete and accurate and can be used for final acceptance and certification of product
Complete Deliverables for Customers and ensure they are complete and accurate
Complete department logs and record yield data as required
Perform preventative maintenance as defined by department maintenance schedule
Support other work areas or departments as required by production or management.
Ability to work overtime as requested
Keep work area clean and organized
Requirements:
Essential Qualifications, Education and Experience:
High school diploma or equivalent
One year of Quality Control experience
Knowledge of AS 9100
Strong work ethic
Ability to work effectively in a team environment
Physical Requirements:
Prolonged periods sitting and performing visual and manual tasks.
Fine motor skills
Ability to use microscopes for long periods of time performing job duties
AdvancedPCB is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, status as a protected veteran, marital status, genetic information, medical condition, or any other characteristic protected by law (EEOC).Compensation: Exact compensation may vary based on skills, experience, and location. About AdvancedPCB, AdvancedPCB is a leading manufacturer of high-reliability printed circuit boards. The company features 6 total manufacturing sites: Santa Clara, our headquarters in the heart of the Silicon Valley; 2 in Southern California, 1 in Maple Grove, Minnesota, Aurora, Colorado and Chandler Arizona. Currently, the company is viewed as over $100 Million; 180,000 sq. ft. of manufacturing space with over 480 employees, making APCT one of the largest privately held printed circuit board manufacturers in North America.
Visit us!*********************
Quality Control Inspector I
Quality control analyst job in Maple Grove, MN
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.
* Responsible for performing 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.
* 2+ years' overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment.
* 1+ year's 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 applying to this position, you consent to receive text messages from the Anteris Talent Acquisition team regarding your application. Message and data rates may apply. You may opt out at any time by replying STOP.
Quality Control Inspector
Quality control analyst job in Chisago City, MN
Job Description
Why Kendall Howard?
We're a growing IT manufacturer with a no-nonsense attitude: stay humble, work hard, and take on challenges head-first. Around here, you won't just “do your job” - you'll be part of a team that builds, solves, and delivers products we're proud to put our name on. The benefits and pay are solid, but the real perk is being part of something that matters alongside people who care just as much as you do.
Our Benefits
We know benefits matter, and we've got you covered. Full-time employees enjoy:
Medical, Dental & Vision coverage
Supplemental insurance options
401(k) with company match
Paid Time Off (PTO)
Paid holidays
Job Summary:
The Quality Control Inspector is accountable for the practical application of the internal Quality Control System. This position ensures that the quality standards as defined by the designers are being met on the shop floor as well as with materials and services supplied by outside vendors.
Essential Functions:
Perform in-process and final inspection activities to ensure all products are manufactured in compliance with work order, traveler, and blueprint specifications.
Develop and maintain inspection reports and documentation.
Measures all parts according to blueprint using Vernier caliper, micrometer, protractor, height gauge, hole and thread gauge, and other tools as needed.
Aids in troubleshooting problems during inspection activities and recommends corrective actions to resolve issues.
Follow up on all cases involving product issues and provide resolution recommendations to Quality Manager, Lean Coordinator, Plant Manager, or Engineering Manager
Maintain periodic inspection schedules to ensure spot checking of production quality.
Maintain 3rd party inspection process.
Maintain the returns and reject re-distribution and scrap procedures.
Minimum Qualifications
1-4 years of experience in the quality field
Experience with blueprints and calibrating measurement tools is required.
Good Oral and written communication skills.
Understanding of the manufacturing process.
The ability to work with minimal supervision.
Strong time management skills.
Monday-Friday
Chemical lab tech
Quality control analyst job in Chanhassen, MN
Chemical lab tech needs 2-3 years of MRP/DRP Planning experience in manufacturing/distribution;
Chemical lab tech requires:
Bachelor's degree or higher in Chemical Engineering, Chemistry, Material Science, Mechanical Engineering or other related fields is preferred.
Ability to gather, understand, and interpret chemical, physical and mechanical data.
Demonstrated ability to partner with other team members in product development programs.
Candidate must be able to work as a team member and also independently on multi-task assignments.
Knowledgeable in Power Point, Word, Lotus Notes, Excel, Microsoft Project and Statistical Analysis Software is preferred.
Chemical lab tech duties:
Conducts all R&D laboratory work in a safe manner including the use of proper Personal Protective Equipment (PPE), adherence to site safety practices, use of laboratory equipment, 5S, etc.
Assists in maintaining project time-lines.
Provides support for various projects assigned by Engineers and/or Supervisor.
Employs basic problem solving skill-sets to overcome project bottlenecks and maintain project deliverable dates.
Collects and organizes data in a coherent format. Communicates basic observations regarding data and/or experimental outcome.
Expected to train other Technicians regarding equipment operation and/or test procedures.
Ability to perform routine tests and operate application equipment safely and efficiently.
Ability to identify abnormalities in collected data and/or project work.
Quality Control Inspector- 1st Shift
Quality control analyst job in Delano, MN
As a valued Trelleborg team member, you will enjoy:
Greater opportunity for impact
Competitive compensation
Generous benefits package: Health, Dental, Vision, STD, LTD, Life, 401k
Paid time off
Bonuses
Pay and Schedule:
$19 - $24 per hour
Hours: 6:00am - 2:30pm Monday through Friday
Qualifications:
High School diploma or equivalent
Required: 0-3 years' experience in manufacturing environment
Desired: Experience with clean room manufacturing
Responsibilities:
Conducts inspections to ensure compliance with product specifications. Inspections include visual, dimensional, functional, and physical testing on product from all departments.
Performs all duties per appropriate work instructions.
Completes required documentation.
Verifies packaging and documents for shipping parts.
Performs accurate data entry.
Collaborates and gathers documentation or data, tests product or materials for root cause analysis, investigations, and drives continuous improvement activities.
Communicates orally in a professional, courteous manner. Written communications should be clear and concise.
Serves as a good team player.
Uses Lean Enterprise methods to reduce waste and complexity in all processes and organizes work area.
Ensures work area is clean and safe.
Assists with filing or scanning for QA Dept.
Able to accurately scan processing records to computer files for archiving.
Quality Control Active Cabinet
Quality control analyst job in Brooklyn Park, MN
Quality Control Active Cabinet
OBJECTIVE: Responsible for quality control of Active Cabinets. Ensures cabinets and related components meet company and customer quality standards throughout the entire production process. Ensures electrical safety in the Active Cabinet Test Area is to OSHA and company standards. Develops and documents the Corrective action process utilizing root cause analysis and troubleshooting techniques. Supports the calibration of all test equipment utilized for the Active Cabinet production process.
POSITION RESPONSIBILITIES
Active Cabinet Test
Skilled in interpreting technical drawings, blueprints, and quality specifications to guide and meet project requirements.
Knowledge working with 240V AC and -48V DC power systems to turn up cabinets for test.
Follow process instructions and quality guidelines to complete Functional Test of Active Cabinets.
Supporting internal and external audits to ensure compliance with company, industry standards (e.g., ISO), and relevant safety regulations.
Actively participating in problem-solving activities, root cause analysis, and continuous improvement efforts to address and resolve recurring quality issues.
Utilize various measuring devices to perform routine measurements and tests.
Troubleshoot and correct Test Failures.
Document Test Failures and Train Assembly Technicians on Test Failure modes.
Learn simple coding to develop Functional Test programs/procedures for new Active Cabinets.
Ability to work independently and accept work direction from Manufacturing Engineer Team, Leads, Supervisor and co-workers.
Performs electro-mechanical assembly when needed.
Collaborate with trainers to support the onboarding and retraining of employees to quality standards and procedures.
Assist in building active cabinets when there is no quality testing to conduct.
Quality Focus
Inspects finished cabinets to ensure they comply with quality specifications and technical drawings/blueprints.
Perform tests and use special equipment to ensure package and product quality
Operate all manufacturing equipment efficiently and safely, related to Active Cabinets production
Maintaining detailed and accurate records of all inspections, test results, and quality data. Identifying defects or non-conformances and reporting findings to production teams, supervisors, and management.
Follow process guidelines and expedite quality concerns to management
Demonstrate flexibility and prioritization of work orders
Work with production/maintenance as necessary to support Active Cabinet department
Following Standard of Operations Procedures (SOP s) and WIO s
Inspect, test, or measure materials or products being produced
Utilize correct measuring tools for product build and quality inspections.
Accept or reject finished items according to quality standards and guidelines
Remove all products and materials that fail to meet specifications
Monitor quality standards for all manufactured products
Record the results of inspections through test reports.
Report inspection and test data
Detailed focused to identify flaws and/or deviations from design specifications
Ensure clean work area through good housekeeping practices throughout shift
Assess and verify the accuracy and functional statues of measuring equipment.
Proficiency in quality control and corrective action, non-conforming products, processes, and equipment.
COMPETENCIES:
Initiative: Dealing with situations and issues proactively and persistently, seizing opportunities that arise.
Brings issues to the attention of appropriate personnel as needed
Offers ideas or suggests modified approaches to address current situations or issues.
Undertakes straightforward tasks that go beyond the job's routine demands (e.g., helps others when own work is completed), without being prompted.
Problem Solving: Identifying problems and the solutions to them.
Identifies alternate solutions, considering applicable precedents.
Identifies optimal solutions based on weighing the advantages and disadvantages of alternative approaches.
Evaluates the effectiveness and efficiency of solutions after implementation.
Attention to Detail: Working in a conscientious, consistent and thorough manner.
Seeks out others to check or review own work for accuracy and completeness.
Verifies assumptions and information before accepting them.
Review all relevant information or aspects of a situation before taking action or making a decision.
Teamwork: Working collaboratively with others to achieve organizational goals.
Initiates collaboration with others.
Assumes additional responsibilities to facilitate the achievement of team goals.
Seeking input from other team members on matters that affect them.
POSITION REQUIREMENTS:
Three plus years of Quality Control experience or relevant experience preferred
Five plus years of manufacturing, or light electrical assembly is preferred
Strong attention to detail
Ability to identify colors, and strong eye-hand coordination.
Operating testing instruments preferred
General assembly experience,
Basic electric testing concept
Ability to work with a wide variety of part sizes and weights
Extensive dexterity and hand, wrist, and arm movement
Ability to work in a fast-paced environment.
Ability to read and understand written instructions, basic arithmetic skill and electrical schematics.
Strong communication and problem-solving skills.
Intermediate skill level in both Microsoft Office Suites and computer navigation
Continuous improvement mindset, Lean Sig Sigma training, yellow belt preferred.
Change Management mindset
Safety mindset
Role requires standing or walking for extended periods of time
Able to lift up to 50 lbs.
Forklift Certified, is a plus
BENEFITS for full time:
Comprehensive Medical, Dental, and Vision benefits.
100% company paid Short-term and Long-term disability insurance coverage.
100% company paid Basic Life and Accidental Death and Dismemberment (AD&D) insurance coverage.
100% company paid Business Travel Accident (BTA) insurance.
100% company paid Employee Assistance Program (EAP).
Additional voluntary benefits are offered.
401K plan: Maximum match is 4.5% of the first 6% of contribution.
Employee Stock Purchase Plan:
Clearfield's Time Off Policy includes Personal Time Off (PTO) beginning at three weeks annually. PTO is accrued on the first of the month starting on day of hire. In addition, nine paid holidays per year.
Hourly Salary Range: Starting rate $ 26.00 per hour, Retention Bonus, and Semi-Annual Production Bonus
An Offer of employment will be extended at a level consistent with the experience and qualifications of the candidate. This information reflects the anticipated salary range for this position at the time of posting. The salary range may be modified in the future and actual compensation may vary from the posting based on various factors such as geographic location, work experience, education and/or skill level.
Quality Control Technician 3
Quality control analyst job in Saint Paul, MN
The Quality Control Technician is responsible for laboratory and field testing of materials primarily focusing on asphalt mixes and aggregates. This role is critical to the successful execution of the Airfield Projects and involves frequent travel to job sites across the Pacific and continental U.S and any other location as business dictates. The position requires experience in laboratory procedures, equipment calibration, data integrity, and field test coordination. This individual serves as a key technical contributor within a high-stakes, federally governed infrastructure project.
Essential Duties and Responsibilities
Reasonable accommodations or workable solutions may be made to enable individuals with disabilities to perform essential functions.
• Perform asphalt laboratory testing including extraction, gradation, compaction, and performance assessments in accordance with ASTM, AASHTO, and/or USACE procedures.
• Coordinate daily with project engineers and other technical staff to ensure accurate scheduling, execution, and documentation of test results.
• Operate and maintain laboratory and field testing equipment.
• Produce accurate, legible, and timely testing documentation that supports client reporting and project requirements.
• Contribute to troubleshooting, quality assurance, and process improvement for large-scale material testing programs.
• Represent AET with professionalism and technical integrity while embedded on federal or client job sites.
• Travel frequently and maintain readiness for long-duration field assignments in remote or high-security locations.
• Adhere to all federal, site-specific, and AET safety protocols with a zero-tolerance approach to noncompliance.
Supervisory Responsibility
This position may informally guide or mentor junior technicians on specific assignments but does not include formal supervisory authority.
Qualifications and Education Requirements
Associate degree or higher in Construction Technology, Civil Engineering, Materials Science, or a related field and a minimum of 1 year of direct asphalt laboratory or field testing experience. Or High school diploma or equivalent and a minimum of 3 years of progressive asphalt laboratory or field testing experience.
Must be eligible to work in high-security environments (e.g., military bases) and pass background screening.
Valid driver's license with clean driving record and ability to travel extensively.
Ability to work extended shifts, including nights and weekends, in remote field environments.
Preferred Skills
Airfield Asphalt Lab Technician Certification from NCAT
ACI Aggregate Testing Technician Level I and/or Level II
FAA or Department of Defense project experience.
Strong familiarity with MS-2 Asphalt Institute Asphalt Mix Design Methods/FAA P-401/P-403 mix designs and testing protocols.
Demonstrated ability to work independently in remote locations with minimal supervision.
Experience collaborating with diverse project teams across geographic regions.
Pay Transparency
At AET, we value transparency-from expectations to compensation. This Field Technician role offers a base hourly wage of $28.00 to $34.00, based on skill set and experience. With guaranteed overtime, bonuses, incentives, and travel per diems, total annual compensation can reach up to $146,000.
We provide a comprehensive benefits package that includes health insurance, ESOP, 401(k) with match, life insurance, disability coverage, PTO, and professional development opportunities.
Ideal candidates bring technical field experience, are reliable and safety-focused, and work well in teams. You must be authorized to work in the U.S. without visa sponsorship.
Join AET and be part of a company that values your contributions, supports your growth, and rewards your impact.
Work Environment
This job primarily operates in both laboratory and field environments. The role includes working in temporary field labs, airport job sites, and secure federal locations with tight operational windows and strict compliance oversight.
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands or fingers, handle or feel; and reach with hands and arms. The employee is occasionally required to sit; climb or balance, and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.
AAP/EEO Statement
It is the policy of AET to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.
Auto-ApplyResearch & Development (R&D) Technician
Quality control analyst job in Eagan, MN
Full-time Description
The R&D Technician will support the formulation and development of cosmetic and OTC personal care products, with a focus on skincare and suncare. This role involves preparing and modifying formulations under the guidance of R&D Chemists, performing lab tests, documenting processes, and supporting scale-up activities. The technician must adhere to lab protocols, ensure compliance with regulatory guidelines, and maintain a clean and safe laboratory environment. This position reports directly to the VP of R & D and plays a key role in bringing innovative, high-quality products from concept to launch.
Key Responsibilities:
Prepare lab batches based on new or modified formulations according to directions from R&D Chemists and Management.
Assist in formulation adjustments to meet product performance, stability, and regulatory requirements.
Conduct routine testing of lab batches, including pH, viscosity, specific gravity, appearance, texture, and odor.
Maintain accurate and organized records of all formulation work, testing data, and observations.
Ensure all samples and documentation meet internal standards and are archived appropriately.
Gain familiarity with regulations related to OTC and cosmetic products, including FDA monograph requirements.
Support scale-up and pilot batching processes, and assist in the transfer of formulas to the production floor as requested by the chemists and R & D management
Learn and follow proper procedures for weighing, mixing, and batching raw materials in accordance with Good Manufacturing Practices (cGMP).
Identify and communicate any issues during batching, testing, or stability evaluations to the chemists
Maintain cleanliness, safety, and organization in the lab environment, including routine maintenance of lab equipment.
Work on multiple development projects simultaneously and manage shifting priorities as needed.
Requirements
Required Skills/Abilities
Hands-on experience with laboratory equipment and processes
Knowledge of safe chemical handling procedures.
Ability to accurately perform calculations for batching and scaling.
Strong attention to detail, organizational skills, and commitment to documentation accuracy.
Effective written and verbal communication skills.
High level of initiative and problem-solving ability in a fast-paced environment.
Ability to work both independently and collaboratively as part of a cross-functional team.
Proficient in Microsoft Office (Excel, Word, Outlook).
Willingness to learn and adapt quickly to new methods, regulations, and technologies.
Required Education and Experience
Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related scientific discipline.
Preferred Education and Experience
Experience working within cosmetic or OTC product environment under FDA regulations (e.g., sunscreens, acne treatments, antiperspirants).
Familiarity with GMP documentation practices and regulatory compliance requirements.
Bachelor's degree in Chemistry or Cosmetic Science or advanced training in formulation chemistry.
Salary Description $20/hr - $29/hr
Quality Control
Quality control analyst job in Andover, MN
Journey Auto Repair is looking to add the right "someone" to our growing team!
You will be playing an essential role in the day-to-day operations with opportunities to learn skills in the Automotive Repair Trade. You are the last line of defense for us to ensure continued, high-quality service and support to our amazing customers. You will be able to help us catch preventative situations and provide a "leave it better than you found it" service before customers pick up their vehicles from our shop. Minor interactions with customers will occur and people will know your name!
You will start as a shop porter/assistant/helper.
Job Duties:
Completion of Quality Control process on Repaired vehicles
Conduct Test Drives Perform Mini-detailing service
Shuttle Customers
Help with shop cleanliness
Other Duties as assigned
Hours and Compensation:
Monday-Friday 7:30am-5:30pm
$14-$18
Job Type: Full-time
Pay: $14.00 - $18.00 per hour
Education:
High school or equivalent (Preferred)
License/Certification:
Driver's License (Required)
Proficient operation of manual and automatic transmission vehicles
Work Location: In person
Job Type: Full-time
Work Location: In person
QC Chemist
Quality control analyst job in Eden Prairie, MN
The Quality Control Chemist will perform testing and evaluations of raw material, bulk, and finished products in accordance with written procedures. This role requires ensuring current standard operating and test procedures are utilized, maintaining accurate documentation records in compliance with GMP requirements, and developing an understanding of various testing methodologies. The position is crucial in maintaining product quality specifications and customer standards, ensuring test results meet specifications, and performing batch adjustments as needed.
Responsibilities
* Conduct testing and evaluations of raw materials, bulk, and finished products according to written procedures.
* Ensure utilization of current standard operating and test procedures.
* Maintain accurate documentation records in compliance with GMP requirements.
* Develop and maintain understanding of testing methodologies, techniques, and potential errors.
* Ensure product quality specifications and customer standards are met and maintained.
* Perform batch adjustments and troubleshoot out of specification situations.
* Update test procedures and specifications as needed.
* Utilize data to focus improvement efforts to meet customer requirements and regulatory regulations.
* Accurately record all data and pertinent information.
* Document Key Quality Incidents and out of specification situations, determine root cause, and suggest solutions.
* Maintain compliance with regulatory expectations and practices.
* Promote a culture of 'lean action' within the department.
Essential Skills
* Laboratory skills
* Chemistry degree
* 0-6 months of industry experience
* Wet chemistry
* FTIR
* Quality control
Additional Skills & Qualifications
* 4 year degree in chemistry
* 0-2 years of QC industry experience in pharma, cosmetics, or food
* Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus
Work Environment
The Quality Control Chemist will work at the Eden Prairie site, primarily indoors, with exposure to various fragrances. The position requires 12-hour shifts on Friday, Saturday, and Sunday, with potential opportunities to extend to full 40-hour weeks based on workload. Candidates need to be comfortable working independently, as they will be the sole person in the lab but can collaborate with a counterpart at the Chaska facility. The role demands moderate to high physical activity and adaptability to changes in a high-paced work environment. Available shifts include 6pm - 6am (preferred), 7pm - 7am, and 8pm - 8am. Benefits include 2 days of billable accruable vacation, 6 days of billable holiday pay, and billable sick pay.
Pay and Benefits
The pay range for this position is $25.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Eden Prairie,MN.
Application Deadline
This position is anticipated to close on May 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.