16 Manufacturing Companies jobs in Lakeville

Job Description

Job Description

Position: Quality Control Manager

Key Responsibilities and Accountabilities:

• Read and interpret specifications, plans, and resource documents to determine

requirements and planning procedures.

• Document and update appropriate logs.

• Conduct, attend and participate in project meetings.

• Obtain, review and submit required submittals and maintain submittal register.

• Obtain, review, write, and submit RFI’s,

• Coordinate Three Phase of Control plan Preparatory, Initial and Final Phases.

• Maintain quality control by frequent and regular inspection of work and work-in-progress.

• Complete all reports and records in an accurate and timely manner.

• Maintain an orderly and clean presence on the jobsite.

• Complete job close-out procedures.

Minimum Qualifications:

• Working knowledge of field construction including systems, practices, general

engineering principals and construction techniques, materials, methods, and

sequencing.

• Familiarity with requirements of USACE EM 385-1-1.

• Experienced with RMS

• Detailed experience with quality control systems.

• Experience in the areas of hazard identification and safety compliance.

• Strong work ethic with a passion to fulfill commitments.

• Sincere obligation to client satisfaction.

• Strong analytical, problem solving, organizational, multi-tasking, communication,

and conflict management skills.

• Computer knowledge in sending emails, daily reports, construction look-ahead

schedules, RFI’s etc.• Degree in Engineering, Architecture, Construction Management, Engineering

Technology, Building Construction or Building Science.

• Combined experience as a Superintendent, QC Manager, Project Manager and/or

Assistant PM.

• Engineer on a similar size and type of construction contract.

• Partnership approach to working with architects and engineers.

• MS Office Suite and Bluebeam knowledge and good computer skills.

• Demonstrated ability to be a team player.

• Self-motivation and time management skills.

• Must be willing to travel.

Previous Experience

Minimum 3 years’ experience as a quality control manager, with a minimum of 3 projects

completed with magnitudes of $1M and up. USACE Experience required. Federal clients (VA,

Military) and working in occupied medical facilities is a plus.

If Interested Email your resume to

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.**
Pay Range:
$40,300.00 - $66,250.00
Position Summary:
Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern. This position is responsible for planning, executing, and managing activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure that all applicable objectives are met, and the product functions as expected. To be successful in this role candidate needs to be skilled in analytical techniques for analysis of biological assays. This position interfaces with Manufacturing, Process Engineering, Product Support, Assay Development and Quality Assurance.
Key Responsibilities:
+ Run QC assays for reagents and consumables.
+ Precise and meticulous observation and recording of all details of QC assay, which are not limited to but including: lot numbers, and physical observations of materials
+ Keep a clean and organized workspace
+ Maintain inventory of reagents and consumables needed to perform QC assays
+ Participate in continuous process improvements efforts
+ Understand and follow appropriate lab protocols
+ Chemical handling and hazards
+ Labeling
+ Safety procedures
+ Department specific SOP's
+ Proper use and maintaining equipment
+ Follow guidelines and comply with all company safety, quality, and training procedures and regulations
+ Perform additional duties as assigned
Education and Experience:
+ Bachelor's degree in Biology, Chemistry, or Engineering with laboratory experience.
+ Associates degree or non- scientific bachelor's with 2+ years' relevant experience working in a quality position for a GMP or life science related industry.
Knowledge, Skills and Abilities:
+ Ability to pipette and maintain records with a high degree of accuracy
+ Work independently with minimal supervision on routine tasks
+ Experience with MS Word, MS PowerPoint, MS Outlook
+ Flexibility to work on multiple tasks with increased effectiveness
+ Strong organizational skills with an attention to detail and quality
+ Ability to support and help others in the team
+ Manages time well and will put in extended time as needed
+ Understanding of basic statistical principles
**Why Join Bio-Techne:**
**We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.**
**We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.**
**We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.**
**We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.**
**We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.**
**We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.**
**Bio-Techne is an E-Verify Employer in the United States.**
**All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.**
**To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.**
Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.
Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**Job Description:**
Sharecare is the leading digital health company that helps people - no matter where they are in their health journey - unify and manage all their health in one place. Our comprehensive and data-driven virtual health platform is designed to help people, providers, employers, health plans, government organizations, and communities optimize individual and population-wide well-being by driving positive behavior change. Driven by our philosophy that we are all together better, at Sharecare, we are committed to supporting each individual through the lens of their personal health and making high-quality care more accessible and affordable for everyone. To learn more, visit  .
Job Summary:
The Quality Control Specialist is responsible for reviewing electronic medical records and conducting quality control on each record to ensure we are within HIPAA (Heath Insurance Portability and Accountability) guidelines. This position requires a high attention to detail, while producing quality work at all times.
Essential Job Functions:
+ Ability to check electronic records for HIPAA compliance, compliance with request and authorization limits
+ Ability to review a document and determine if we have the legal right to release medical records based on HIPAA rules and regulations
+ Communicate questions/issues to Lead/Supervisor
+ Work as a mentor to new employees
+ Adhere to state and Federal Laws for Release of Information (ROI)
Specific Skills/ Attributes:
+ High attention to detail
+ Strong time management skills
+ Ability to work in a fast-paced, production-oriented environment
+ Ability to work well with others within a team environment
+ High level of reliability and productivity
+ Must be computer literate; able to use MS Outlook and other Windows-based programs
+ Excellent communication skills
Qualifications:
+ Minimum of 6 months previous experience in a medical record setting
+ Required to pass an industry related course and exam within six months of hire
HIPAA/Compliance:
+ Maintain privacy of all patient, employee, and volunteer information and access such information only on a need to know basis for business purposes.
+ Comply with all regulations regarding corporate integrity and security obligations
+ Report unethical, fraudulent, or unlawful behavior or activity
+ Maintain current and yearly HIPAA certification.
Information Governance Accountabilities:
+ A high-level understanding of the organization's information governance program and role-specific accountabilities
+ A thorough understanding of role requirements, including policies, procedures and processes, to include how individual work impacts the organization and its strategic and financial goals; and how tasks and projects affect the integrity of the organization's data and information
+ Commitment to discuss questions and recommendations about processes and any observed variations in performing tasks in order to ensure a standardized approach to work and services provided
+ Participation in education as required for corporate compliance and role-specific functions and tasks
Physical Requirements:
+ Ability to sit or stand for long periods of time
+ Physical ability to lift and carry 25 lbs. of materials
+ Manual dexterity and strength sufficient enough to enter information via computer keyboard for long periods of time, to write notes and information needed, and to pick up and hold paperwork, supplies and other items.
+ Eyesight sufficient to effectively read documents and to accurately view information on a computer monitor
+ Speaking and hearing ability sufficient to effectively communicate.
+ Eye/hand coordination, hearing and visual acuity necessary for day-to-day tasks
Sharecare and its subsidiaries are Equal Opportunity Employers and E-Verify users. Qualified applicants will receive consideration for employment without regard to race, color, sex, national origin, sexual orientation, gender identity, religion, age, equal pay, disability, genetic information, protected veteran status, or other status protected under applicable law.
Sharecare is an Equal Opportunity Employer and doesn't discriminate on the basis of race, color, sex, national origin, sexual orientation, gender identity, religion, age, disability, genetic information, protected veteran status,or other non-merit factor.

Quality Control Technician I
Location:
Eden Prairie, MN, US
Job ID:
54495
Category:
Manufacturing & Operations
**Stratasys is a world leader in 3D printing!**
**Stratasys** is leading the global shift to additive manufacturing with innovative 3D printing solutions for industries such as aerospace, automotive, consumer products and healthcare. Through smart and connected 3D printers, polymer materials, a software ecosystem, and parts on demand, Stratasys solutions deliver competitive advantages at every stage in the product value chain. The world's leading organizations turn to Stratasys to transform product design, bring agility to manufacturing and supply chains, and improve patient care.
The **Quality Control Technician I** supports Manufacturing and Engineering by inspecting and testing materials, in-process items, and finished products. Responsibilities include verifying compliance with drawings, specifications, and applicable standards, documenting results, and reporting any deviations or concerns.
**What you will be doing:**
+ Complete mechanical, functional, visual inspection per customer requirements and to demonstrate capability across all stages incoming, in-process, final as trained and directed
+ Initiate and close detailed inspection records of test results in a detail-oriented manner that is easily interpreted and communicated
+ Prepare reports, data as directed, noting any relevant deviations from existing standards
+ Communicate quality or compliance concerns with urgency
+ Support Engineering in conducting experiments as directed
+ Responsible for working in compliance with all Quality Management Systems
+ Ensure test equipment is calibrated and working correctly at each use
+ Generate, update and maintain documentation relating to quality and processes
+ Record data and information required to identity a product, traceability throughout as required by specifications, work instructions etc.
+ Diligently abide by Good Documentation Practices
+ Follow all company safety policies and procedures
+ Attend all required company training
+ Demonstrate commitments to Stratasys Behaviors by leading, acting, and modeling these values
+ Other responsibilities as assigned by the department or manager
**Must have for this role:**
+ Associate's degree (concentration in manufacturing or computer sciences strongly preferred)
+ 2-5 years inspection experience in a production environment
+ Working knowledge of various mathematical concepts including fractions, ratios, and proportions
**Nice to have:**
+ Testing certifications
**Travel required:** 5% between MN Stratasys facilities
**What you will be part of:**
+ **Company Overview -** **Our Culture and Values -** **Our Sustainability "3D Printing a Better Tomorrow"** **_-_** **Our Locations** **_-_** **Check out our Video -** Information:**
At Stratasys we have designed a comprehensive Total Rewards program that goes beyond the basics and supports our People First strategy. When you join Stratasys, you'll gain access to benefits and perks that will support you and your family both inside and outside of work.
For this position, the typical annual starting base salary is from $47,756 to $60,792, which does not include variable incentive pay. This range represents a good faith estimate for this position. Your individual base pay will depend on your skills, qualifications, geographical location, and/or experiences.
In addition to a competitive salary, we offer a comprehensive total rewards package (e.g., Medical, Dental & Vision, Health Savings Accounts, Mental Health Resources etc.), recognition programs, employee stock purchase plan, and 401(k) with company match.
**To perform this job successfully** , an individual must be able to perform each essential duty satisfactorily. Stratasys will provide reasonable accommodations for qualified individuals with disabilities. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
**Stratasys** is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to their protected Veteran or disabled status and will not be discriminated against for their race, color, religion, sex, age, disability, military status, or national origin or any other characteristic protected under federal, state, or applicable local law. Please view Equal Employment Opportunity Posters provided by OFCCP here ( .

Job Description

Job Description

We are seeking a Seasonal Quality Technician to join our team and support the Quality Manager and Quality Technician with day-to-day quality assurance tasks. This role will assist with inspections, documentation, sample collection, and other responsibilities outlined in the job description. When not assisting with quality tasks, this team member will be asked to work in production as a Candy Technician to help support operational needs. It’s a great opportunity to gain hands-on experience in both quality and production within a fast-paced environment. This is a seasonal position expected to last through October 31, 2025.

1. Monitors quality and food safety at each step of manufacture and assembly of finished product by verifying against Maud Borup Product Specification Sheets and pertaining SOPs and programs.
2. Directs Assemblers with positive motivation to produce quality and safe products. Conveys pertinent information to personnel so production continues to flow smoothly and efficiently.
3. Contacts support staff when manufacturing issues arise.
4. In conjunction with Line Leads and Food Safety Manager, directs personnel on startup of new jobs and ensures that special instructions, packing, and quality control requirements are understood and followed.
5. Promotes teamwork and positive relations among all contacts by setting positive examples to their staff.
6. Conducts quality and food safety checks and ensures employees are taking responsibility for making quality decisions.
7. Responsible for working safely and maintaining a safe work environment: attends required training, identifies and reports hazards; wears required PPE for position; and is accountable for self as well as co-worker safety.
8. Understands allergen guidelines and how to properly clean and segregate to keep from cross contamination.
9. Contributes to team effort by accomplishing tasks as needed. Provides strong leadership to production personnel. Maintains a professional appearance and attitude at all times.
10. Ensures food quality and food safety standards are adhered to, understood, and employees know what to do if quality is not within specs or if food safety concerns arise.
11. Is familiar with and complies with SQF Food Safety standards and ensures all product produced meets assigned quality standards.
12. Conducts allergen, ATP and microbial testing as needed.
13. Conducts daily, weekly, and monthly audits as assigned by Food Safety Manager, including but not limited to allergen, organic, GMP, chemical inventory, glass and brittle plastics audits, temperature and humidity monitoring.
14. Responsible for collecting retain samples, cataloging them and assisting Food Safety Manager in reviewing samples upon reaching assigned shelf life.
15. Responsible for scale calibrations and weekly cleaning.
16. Assist Food Safety Manager with preparation for, and provides support during SQF, QAI, GFCO, and other external audits.
17. Back up to Quality Assurance Technician as needed.

7am - 3:30pm M-F

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

Our client, a leading automotive manufacturing company renowned for its commitment to quality and innovation, is seeking a highly skilled and experienced Senior Automotive Quality Control Manager to oversee their quality assurance operations in Minneapolis, Minnesota, US . This critical leadership position will be responsible for establishing and maintaining rigorous quality standards throughout the manufacturing process, ensuring that all vehicles meet or exceed customer expectations and regulatory requirements. The ideal candidate will possess a deep understanding of automotive manufacturing processes, quality management systems, and statistical process control.

Key Responsibilities:

• Develop, implement, and manage comprehensive quality control plans and procedures for automotive production.
• Supervise and mentor a team of quality control inspectors, technicians, and engineers.
• Establish and monitor key quality metrics and performance indicators (KPIs).
• Conduct regular audits of manufacturing processes to ensure compliance with quality standards and certifications (e.g., ISO/TS 16949, IATF 16949).
• Analyze production data to identify root causes of quality issues and implement corrective and preventive actions (CAPA).
• Oversee the inspection and testing of raw materials, in-process components, and finished vehicles.
• Collaborate with engineering, production, and supply chain teams to resolve quality-related problems.
• Manage supplier quality and performance, working to ensure the quality of supplied components.
• Develop and deliver quality training programs for production personnel.
• Lead continuous improvement initiatives to enhance product quality and manufacturing efficiency.
• Manage customer feedback and warranty claims related to quality issues.
• Ensure adherence to all safety regulations and promote a safe working environment.
• Prepare reports for senior management on quality performance and improvement initiatives.

Qualifications:

• Bachelor's degree in Engineering (Mechanical, Electrical, Industrial), Quality Management, or a related field.
• Minimum of 7 years of experience in quality control or quality assurance within the automotive manufacturing industry.
• At least 3 years of experience in a management or supervisory role.
• Proven experience with quality management systems (QMS) such as IATF 16949.
• Strong knowledge of statistical process control (SPC), Six Sigma, and Lean Manufacturing principles.
• Experience with various quality inspection tools and techniques.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong leadership, team management, and communication abilities.
• Proficiency in quality management software and Microsoft Office Suite.
• Ability to interpret technical specifications, blueprints, and quality standards.
• Familiarity with automotive components and assembly processes.
• Six Sigma Green Belt or Black Belt certification is a plus.

Join our client's team in Minneapolis, Minnesota, US , and contribute to building vehicles of the highest quality.

Our client is looking for a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in **Minneapolis, Minnesota, US**. This role is essential in ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and analysis. The ideal candidate will have a strong background in analytical chemistry, pharmaceutical sciences, and a deep understanding of quality control methodologies and regulatory requirements (e.g., cGMP, FDA). Responsibilities include performing a variety of analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, spectroscopy, and wet chemistry. You will be responsible for maintaining laboratory equipment, calibrating instruments, preparing analytical reagents, and documenting all testing procedures and results accurately in compliance with regulatory standards. The successful candidate will also participate in method validation, troubleshoot analytical issues, and contribute to the development and improvement of quality control processes. This position demands excellent attention to detail, strong critical thinking and problem-solving skills, and the ability to work effectively both independently and collaboratively within a team environment. A bachelor's degree in Chemistry, Pharmacy, or a related life science field, coupled with significant experience in pharmaceutical quality control, is required. Experience with Good Manufacturing Practices (GMP) is essential. Come contribute your expertise to the pharmaceutical industry in **Minneapolis, Minnesota, US**, ensuring the highest standards of product quality and patient safety.