Post job

Explore jobs

Find specific jobs

Explore careers

Explore professions

Best companies

Explore companies

Quality control analyst jobs in Apple Valley, MN

- 83 jobs
All
Quality Control Analyst
Quality Control Technician
Quality Control Inspector
Research And Development Technician
Quality Control
Chemist, Development
Quality Control Chemist
Chemistry Laboratory Technician
Quality Control Associate
Quality Control Specialist
Chemical Laboratory Technician

  • Quality control Active Cabinet

    Clearfield Inc. 4.3company rating

    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 (SOPs) and WIOs * 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.
    $26 hourly 2d ago

  • Quality Control Technician 3

    American Engineering Testing Inc. 4.3company rating

    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.
    $28-34 hourly Auto-Apply 60d+ ago

  • Quality Control Analyst II

    Lancesoft 4.5company rating

    Quality control analyst job in Brooklyn Park, MN

    Job Title: Quality Control Analyst Microbiology Duration: 11 Months Schedule 8 AM to 5 PM Independently execute and review routine in-process, drug substance, and stability test methods in a timely manner. Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS, SoftmaxPro, Charles River Endoscan, MODA, and Empower). Maintain lab operations (including cleaning, ordering of supplies, reagent preparation, stocking, waste disposal). Conduct test methods including samples generated for facility monitoring (i.E., Environmental Monitoring and Critical Utilities), in-process, drug substance, and stability. Own and author quality system events (i.E., laboratory investigations, deviations, CAPA s and change controls). Responsibilities: Job Function and Description Demonstrate a functional and basic theoretical understanding of laboratory operations and Standard Operating Procedures (SOP s). Work within laboratory environment for extended periods of time, conducting facility monitoring (i.E., Environmental Monitoring and Critical Utility Monitoring) and product tests, reviewing data, maintaining laboratory materials and instruments and other laboratory functions as required. Complete all testing, including special project and protocol testing in a timely and appropriate manner. Maintain data integrity and ensure compliance with company SOP s, specifications, and cGMP regulations. Independently exercise judgment within generally defined Quality Control (QC) procedures and practices in selecting methods and techniques to troubleshoot problems and/or formulate solutions. Decisions have moderate impact on future QC processes and procedures that impact batch disposition. Initiate and own laboratory investigations, basic complexity low and medium risk deviations, CAPA s, and change controls of moderate scope within the electronic Quality Management System. Participate in cross-functional teams. Draft studies and investigations of moderate scope and work on problems where the situation or data requires a review of identifiable factors. Author new SOP s and initiate changes to existing procedures. Train new QC Analysts on routine procedures and practices. May be required to work overtime or be assigned to a different shift as needed. Perform equipment maintenance and calibrations as required. Complete mandatory training within required timeframe. Perform other duties as assigned. Education and Experience Requirements Bachelor s or master s degree in any Life Sciences with relevant laboratory coursework 3-6 years of relevant experience preferred. Previous experience in a regulated environment preferred. Must understand laboratory instrumentation. Must be able to communicate effectively with managers and peers. Must be able to read, write, and converse in English. Must have basic computer skills. General use of word processing, spreadsheets, databases, etc. For the purposes of work execution, training, performance management, and self-service. Good interpersonal skills and able to work effectively and efficiently in a team environment. Knowledge of cGMP manufacturing Knowledge of chemical, biological and/or microbiological safety procedures. Must display eagerness to learn and continuously improve. Key Skills, Abilities, and Competencie Additional skills include, but are not limited to: QC Micro Skill Set Contamination control, Endotoxin, Bioburden, Environmental Monitoring, Manufacturing Cleanrooms, Aseptic Technique, Critical Utility systems Complexity and Problem Solving Employee at this level is involved in routine tasks of moderate scope and complexity. Employee receives instructions on new work and refers to policies and procedures for guidance. Responsible for conducting independent work with minimal guidance from trainers and more senior staff. Responsible for contributing to moderate scope decisions founded on sound principles, international industry/regulatory standards, and robust scientific basis. Understand the needs of key collaborators (i.E., Manufacturing Operations, Quality Assurance, Validation and Quality Systems) to provide compliant and timely test results. Internal and External Contacts Participate in cross-functional collaboration with internal departments (i.E., Quality, Manufacturing, Engineering, Metrology, and Business Excellence). Other Job Requirements Physical Demands: Stand or sit -? Must be able to remain in a stationary or standing position for extended periods of time in both office and laboratory environment. In certain areas of QC, the following may apply: Carry weight, lifting - Frequently moves laboratory materials and portable instruments weighing up to 30 pounds. Climb - Occasionally ascends/descends step ladders to reach materials and/or stairs to collect samples. Dexterity/balance required to gown for cleanroom work, balance and dexterity are required. Other / Travel Requirements: May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection. May be required to participate in an on-call rotation for off-shift coverage or occasionally work off-shift hours to help support a 24-7 manufacturing department. Willingness to travel to various meetings or training, this could include overnight trips. Requires 0-5% travel.
    $63k-81k yearly est. 25d ago

  • Principal Research and Development Technician

    Freudenberg Medical 4.3company rating

    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
    $51k-73k yearly est. Auto-Apply 32d ago

  • Method Development Chemist

    Integrated Resources 4.5company rating

    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
    $62k-80k yearly est. 60d+ ago

  • Research & Development (R&D) Technician

    Bell International Laboratories 4.6company rating

    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
    $20 hourly 60d+ ago

  • QUALITY CONTROL TECH. I

    Wells 4.1company rating

    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 . ” 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
    $25-27 hourly 15d ago

  • Quality Control Technician

    Image First of Iowa

    Quality control analyst job in Bloomington, MN

    Job Details Archetype - Minnesota - BLOOMINGTON, MN $18.00 - $26.00 HourlyDescription We are looking for a meticulous and hands-on Quality Control Assembly Technician to join our sign manufacturing team. This role ensures that all fabricated and assembled signage meets company and client specifications for quality, durability, and visual appeal. The ideal candidate will have experience in inspecting custom signage components including electrical, structural, and aesthetic elements. Key Responsibilities: Inspect assembled signs for accuracy, quality, and compliance with design specifications and industry standards. Verify proper installation of lighting components (LEDs, transformers, wiring) and ensure electrical safety. Check alignment, finish, and structural integrity of sign components including frames, faces, vinyl, and mounting hardware. Use measuring tools and visual inspection techniques to confirm dimensions and tolerances. Document inspection results and report defects or deviations to production and engineering teams. Collaborate with fabricators, assemblers, and installers to resolve quality issues and improve processes. Maintain inspection records and contribute to continuous improvement initiatives. Ensure compliance with safety protocols and company quality standards. Qualifications High school diploma or equivalent; technical training in fabrication, electrical, or mechanical fields preferred. 1-3 years of experience in quality control or assembly in a sign manufacturing or related industry. Familiarity with sign materials (e.g., acrylic, aluminum, vinyl, LED systems) and fabrication techniques. Ability to read and interpret shop drawings, blueprints, and wiring diagrams. Strong attention to detail and problem-solving skills. Basic computer skills for documentation and reporting. Good communication and teamwork abilities. Working Conditions: Work performed in a fabrication shop and warehouse environment. May require standing, bending, and lifting up to 50 lbs. Use of PPE including safety glasses, gloves, and hearing protection as needed. EEO STATEMENT: Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, disability, age, marital status, or status with regard to public assistance.
    $37k-49k yearly est. 60d ago

  • QC Line Tech, 1st shift

    Reckitt Benckiser 4.2company rating

    Quality control analyst job in Wanamingo, MN

    We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role Quality technicians, also known as Quality Control Technicians, are junior-level employees who perform quality control checks on company products to ensure they meet required safety and quality standards. Quality technicians are provided with on-the-job training but require a keen eye for detail and the ability to focus for extended periods. Schedule - Monday - Friday 6:00 AM - 2:00 PM Your responsibilities * Understand and meet customer specifications, requirements, and expectations * Have good understanding of the processing procedures and sequence of event timing involved with manufacturing a given product * Obtain the ability to collect samples and perform required testing as necessary. * Understand and implement all elements of environmental program * Document test results for finished goods, raw material, environmental and all other tests * Ensure that equipment is properly calibrated and sample materials are prepared to meet scheduled requirements * Understand and follow Food Safety programs, GMP's, SOP's, HACCP (Hazard Analysis and Critical Control Points), sanitation and pest control programs and contact customer operating procedures * Notify all pertinent personnel of problems or potential problems * Understand and implement HOLD procedure to isolate product or raw material that deviates from specification * Maintain work area and equipment in clean and orderly manner * Make reagents necessary for lab procedures * Oversee immediate production issues, follow-up as necessary, HOLD product * Work efficiently with personnel in other departments * Support and assist Sanitation requirements to ensure compliance * Act as backup for other quality personnel during vacation, planned absence and sick time * Perform miscellaneous duties as assigned by Leadership. * Operate equipment as needed to support Operations. The experience we're looking for * Must have good verbal and written communication skills and the ability to read and understand instructions * Must be a self-starter capable of working without supervision * Must be detail oriented and to work accurately and precisely * Must be willing to take ownership and accept responsibilities of QA (Quality Assurance) functions * Must be able to multi-task * Possess a high degree of personal cleanliness * Possess well-developed sensory skills * Possess organization and prioritization skills and the ability to manage time well * Must be able to perform basic computer functions (Word/Excel) * Prefer experience in food manufacturing and /or quality control What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact ******************************* .Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Red Wing Job Segment: Nutrition, Counseling, Healthcare
    $56k-67k yearly est. 18d ago

  • Quality Control

    Journey Auto Repair

    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
    $14-18 hourly 8d ago

  • Quality Control Inspector I

    Anteris Tech

    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.
    $22-28 hourly 18d ago

  • Chemistry Laboratory Technician

    Actalent

    Quality control analyst job in Minneapolis, MN

    As a QC Laboratory Technician, you will play a crucial role in ensuring the quality of our products meets established standards and specifications. You will learn the fundamentals of coatings technology, conduct experiments, and compile test results and analyses. Your work will involve performing lab tests to assist scientists in material analysis and documenting findings. Additionally, you will actively participate in safety programs and audits to maintain a safe work environment. You will also be involved in mixing paint batches according to formulas or developing new experimental formulas, maintaining lab equipment, and performing some ICP-MS work as part of your training. Responsibilities + Ensure product quality meets standards and specifications. + Learn the basics of coatings technology and compile test results and analyses. + Conduct experiments and tests using standard paint procedures and techniques. + Perform lab tests to assist scientists in material analysis and document findings. + Participate in safety programs and audits to maintain a safe work environment. + Mix paint batches according to formulas or create new experimental formulas. + Maintain lab equipment and areas, including routine upkeep of specific rooms and cabinets. + Perform some ICP-MS work as part of training. Essential Skills + 1-3 years of related experience or a Bachelor's degree in Chemistry, Biochemistry, or similar. + Strong communication and interpersonal skills with proficiency in English. Job Type & Location This is a Contract to Hire position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $22.00 - $24.00/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 Minneapolis,MN. Application Deadline This position is anticipated to close on Dec 15, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.
    $22-24 hourly 11d ago

  • Quality Control Inspector PCB Manufacturing

    Advancedpcb

    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!*********************
    $34k-46k yearly est. 11d ago

  • Quality Control Inspector

    Kendall Howard

    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
    $34k-46k yearly est. 14d ago

  • Quality Control Inspector I

    Anteris Technologies Global Corp

    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.
    $34k-46k yearly est. 46d ago

  • Chemical lab tech

    Globalchannelmanagement

    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.
    $39k-49k yearly est. 60d+ ago

  • Quality Control Specialist

    Phillips Medisize 4.7company rating

    Quality control analyst job in Hudson, WI

    Your Job Phillips Medisize, a Molex company is seeking a Drug Logistics Material Specialist to join our team at our Hudson, WI site. In this role, you will play a vital role in maintaining the accuracy and compliance of drug product inventory within temperature-controlled environments. This role offers the opportunity to contribute innovative solutions to optimize drug logistics operations within a dynamic pharmaceutical manufacturing environment. Our Team Phillips Medisize is an end-to-end provider of innovation, development, and manufacturing solutions to the pharmaceutical, diagnostics and medical device industries. Our team at Hudson, WI is made up roughly of 300 employees that support our production, Engineering, Quality, Molding & Tooling departments. What You Will Do Ensure all drug products are accurately tracked entering and leaving storage areas, keeping records audit-ready and compliant with regulatory standards. Collaborate with project teams to complete all required documentation for new or updated products, including chemical reviews, hazard worksheets, inventory forms, and impact assessments. Work closely with project teams, warehouse, operations, and engineering to facilitate smooth product receipt, staging, and readiness for processing. Monitor inventory levels, fulfill drug requests promptly, and coordinate with purchasing to maintain optimal stock, including related materials such as data loggers and transport carts. Manage timely receipt and proper storage of drug products, prioritize urgent items to prevent delays, and prepare finished products for shipment following all compliance protocols. Perform regular temperature mapping and monitoring of drug storage locations (including coolers), ensuring adherence to temperature standards and coordinating with calibration teams. Conduct regular inventory cycle counts, investigate discrepancies, and execute ERP system transactions to maintain real-time inventory status and accurate labeling. Maintain organization and segregation of walk-in cold rooms and drug storage areas per FIFO, quarantine, rejected, and approved classifications. Ensure all procedures are standardized, consistently applied, and documented; develop innovative solutions to address operational challenges and unforeseen issues. Who You Are (Basic Qualifications) 3+ years of experience in quality within the pharmaceutical, medical device, or biotechnology industry 2+ years of direct experience in drug manufacturing Experience in quality management tools, methodologies (e.g. risk management, root cause analysis, FMEA), and software systems What Will Put You Ahead Ability to work effectively with cross-functional teams such as Quality Engineers, Manufacturing Engineers, and Operations. Experience with tracking TOR (Time Out of Refrigeration) for drug products. This position does not qualify for VISA Sponsorship. In order to comply with U.S. export control laws and regulations, this position requires applicants to either provide proof of U.S. citizenship or lawful permanent resident status or be eligible to receive an export authorization (a license) under the International Traffic in Arms Regulations and/or the Export Administration Regulations. At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy. Hiring Philosophy All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds. We are Military Ready and Second Chance employers. Learn more about our hiring philosophy here . Who We Are As a Molex company, Phillips-Medisize mobilizes and deploys specialized capabilities and services across highly regulated industries, including health care, regulated consumer, automotive and defense. We design, develop and create innovative and life-changing medical technologies for millions of people around the globe. At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company. Our Benefits Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most. Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance. Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region. If you have questions on what benefits apply to you, please speak to your recruiter. Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results. Equal Opportunities Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, some offers of employment are conditioned upon successfully passing a drug test. This employer uses E-Verify. Please click here for additional information. (For Illinois E-Verify information click here , aquí , or tu ).
    $25k-36k yearly est. 8d ago

  • Quality Control Inspector- 1st Shift

    Trelleborg Sealing Solutions 4.6company rating

    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.
    $19-24 hourly 23d ago

  • QC Chemist

    Actalent

    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.
    $25-26 hourly 60d+ ago

  • Quality Control

    Journey Auto Repair

    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
    $14-18 hourly 8d ago

Learn more about quality control analyst jobs

How much does a quality control analyst earn in Apple Valley, MN?

The average quality control analyst in Apple Valley, MN earns between $38,000 and $95,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.

Average quality control analyst salary in Apple Valley, MN

$60,000
Job type you want
Full Time
Part Time
Internship
Temporary
Quality Control Analyst jobs by location
Popular quality control analyst job locations
Quality Control Analyst related jobs
Related jobs nearby