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A Health, Beauty and Cosmetic Manufacturing Client is looking for a direct hire, Quality Engineer onsite in Eagan, Minnesota. The objective of this role is to improve quality within production to meet our customer’s needs and expectations. This Quality Engineer will focus on process and equipment improvements, develop quality control systems and processes, and attack quality system failures using effective root cause analysis methods. Additionally, this role will concentrate on continuous improvement through the implementation of effective Corrective and Preventive Actions (CAPA). The Quality Engineer will play a key role in ensuring that products meet industry standards, regulatory requirements, and internal quality objectives, while promoting a culture of compliance and continuous improvement across the organization. Responsibilities Lead quality-related problem-solving and root cause analysis in manufacturing to prevent recurrences. Lead process validation, equipment qualification,

A contract manufacturer and injection molding client is looking to hire a Senior Quality Engineer in Forest Lake, Minnesota. This quality professional would sit 100% onsite and ideally comes from a plastic injection molding background. Skills Needed: Bachelor’s degree in engineering or related field, or equivalent experience in a contract manufacturing environment, preferably in regulated industries. 8 years of experience in quality engineering Experience with med devices, plastic injection molding and/or contract manufacturing Duties of Position: Work cooperatively with all employees in a team environment Serve as the quality representative on cross-functional new product development teams. Review all documents and specifications referenced on the drawing or purchase orders, identify concerns and communicate to the cross-functional new product development team. Drive drawing and specification changes needed to effectively transfer projects to production. Proactively lead and anticipat

Colder Products Company (CPC) is the leading provider of quick disconnect couplings, fittings and connectors for plastic tubing. At CPC, we believe that fluid handling should be safe and easy. We engineer our connection solutions to improve the overall functionality and design of equipment and processes for the life sciences, industrial, and chemical handling markets. Special features of our products include precise hose barbs for superior grip, built-in shutoff valves for preventing spills, and easy-to-use, push-button thumb latches for quick connecting and disconnecting. CPC is a Dover company based in Minnesota (Minneapolis/St. Paul metro) with global offices and operations in Europe and Asia. Summary: The Customer Quality Engineer is responsible for resolving released product quality issues. This role will collaborate across CPC Quality, Product Management, Operations and Engineering to investigate and resolve customer complaints. This individual will work with the Customer Quality

Job Description Job Description The objective of this role is to improve quality within production to meet our customers’ needs and expectations. The Quality Engineer will focus on process and equipment improvements, develop quality control systems and processes, and attack quality system failures using effective root cause analysis methods. Additionally, this role will concentrate on continuous improvement through the implementation of effective Corrective and Preventive Actions (CAPA). The Quality Engineer will play a key role in ensuring that products meet industry standards, regulatory requirements, and internal quality objectives, while promoting a culture of compliance and continuous improvement across the organization. The Quality Engineer will lead the process validation, equipment qualification, and cleaning validation activities for the Quality Assurance Department. Responsibilities Lead quality-related problem-solving and root cause analysis in manufacturing to prevent recur

Job Description Job Description Primary Objective of Position To support the Engineering job functions of Quality Assurance to meet customer and organizational objectives in one of Intek’s three major value streams. Develops Quality Systems and processes; collaboratively supports value stream team; resolves quality problems; evaluates quality systems applications and equipment; assures product quality; prepares technical performance reports. Provide technical leadership and direction to Associate QE’s, Supervisors, Leads and Operators to foster learning and growth for potential future assignments. Collaborates with company personnel to ensure compliance to company and customer speci-fications and expectations; and assists with the overall implementation and ongoing support of the Intek Plastics, Inc. Quality Management System (QMS). Major Areas of Responsibility To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accomm

Manufacturing Engineer (Contract) RESPONSIBILITIES Developing, implementing, and continuously improving manufacturing processes to enhance yield, reduce costs, and improve productivity. Representing Process Engineering in R&D and Project Team meetings, providing technical expertise in technology transfers, analytical method development, validation, and process scale-up. Conducting or managing process validations (IQ/OQ, OQ, PQ). Troubleshooting production line issues related to yield, quality, and throughput. Leading scaling up processes from development to full-scale manufacturing. Supporting evaluation of NCMR, CAPA, SCAR, Failure Investigation, and Deviation requests from Contract Manufacturers/Suppliers. Creating/updating manufacturing instructions, routings, bills of materials, and SOPs. QUALIFICATIONS Minimum 4-5+ years of experience of medical device manufacturing. Experience with Design Transfer and Process Validations at external suppliers (CMO). Write and execute associated v

About the Company - Our client is a leader in the Plastic Injection Molding industry specializing in Medical Device and other custom manufactured parts. About the Role - We are currently looking for a Quality Engineer to lead development activities, including supporting part validation, qualification, and sustaining programs. This position will also act as a primary contact for customer quality concerns and supports the production and engineering departments in resolving these concerns. Salary: $85k - $100k Responsibilities Participates in the organization’s overall Stage-Gate approach to product realization. Has Responsibility for APQP and PPAP activities for new and changed programs as directed by the Quality & Regulatory Manager. Conducts training as requested and/or needed pertaining to the Quality Management System. Carries out Quality Planning: Process Flow Diagrams, Process FMEA, and Process Control Plan. Prepare work instructions and Inspection instructions. PPAP / validation f

TOMZ Corporation, a leader in manufacturing of devices and components for major medical device companies, is looking for a driven and highly motivated Quality Engineering Technician to join our organization. TOMZ offers competitive compensation and excellent benefits, including 401k, health/dental, vision and paid time off. TOMZ maintains a modern, clean, and safe facility with state-of-the-art equipment and dedication to continuous process improvement. TOMZ is registered with the FDA as a Class 2 and Class 3 Medical Device Manufacturer and is certified to ISO 13485. SUMMARY OF POSITION: This position will be responsible for the activities associated with Inspection/Test Method development and improvement. This role will be expected to collaborate with Quality Engineering to support sustaining manufacturing and product development. ESSENTIAL FUNCTIONS: Must be knowledgeable of, and adhere to, the TOMZ Quality Management System. Programming automated metrology systems such as CMM’s and