Manager, Quality Salary at Welly BETA

🌟 Now Hiring: Senior Manager – Quality Systems🌟 📍 Minnetonka, MN | On-Site | 55343 💼 Contract Duration: 1 Year 💵 Pay Rate: $75–$78/hr (W2) 📍 Location: Minnetonka, Minnesota 55343 (On-Site) Join a mission-driven team making a real difference in healthcare! We’re seeking a Senior Manager – Quality Systems to lead quality initiatives at the forefront of the life sciences industry. This is a high-impact role within a dynamic organization committed to product excellence, patient safety, and regulatory compliance. 🔍 Position Overview As the Senior Manager – Quality Systems, you will oversee and enhance our Quality Management System (QMS), ensuring compliance with FDA and international standards. You’ll lead audits, drive system harmonization, manage product release processes, and oversee equipment administration across cross-functional teams. You’ll thrive here if you're strategic, detail-oriented, and passionate about advancing healthcare through quality systems excellence. ✅ Key Res

Job Title: Engineer Sr, Manufacturing Job Location: Plymouth MN 55442 Job Duration: 12 Months Job Responsibilities: Briefly state the main purpose and scope of the position. This position will design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality. Essential Functions: List the significant/essential duties, tasks or responsibilities which employees in this position are actually required to perform. Manage projects which include new production equipment, process improvements and cost reductions while supporting new product introductions. Provide guidance to other engineers and technicians. Provide technical mentorship to engineers and technicians Conduct Process FMEAs and Process Validations Improve product quality, labor efficiency, and throughput through the use of Lean manufacturing concepts Coordinate the design, procurement, build and debug of tooling, machinery and test equipmen

Quality Assurance Specialist – Plymouth, MN The role is responsible for providing Quality Assurance support and collaborates closely with other departments on investigations and Corrective Action Preventative Action (CAPA). It also involves assisting in regulatory, customer, and certification audits, as well as data collection and participating in external and internal audits. Responsibilities: Facilitate annual GMP training alongside department liaisons. Investigate and communicate customer complaint resolutions. Conduct monthly facility walkthroughs and report findings. Address process failures via the company deviation process. Oversee the internal audit program, ensuring documentation, procedures, data, facilities, and systems comply with dietary supplement regulations (CFR Title 21, Part 111, NSF/ANSI 173-2003). Promote Safety policies and address/report hazards. Ensure timely review/closure of open CAPAs. Act as back-up contact for the Gluten Intolerance Group (GFCO). Aid in regu

Job Description Job Description About the Role: The Quality Inspection - Team Lead will play a crucial role in ensuring that all products meet the highest standards of quality and safety before they reach our customers. This position involves overseeing a team of quality inspectors, providing guidance and support to ensure compliance with industry regulations and company policies. The Team Lead will be responsible for developing and implementing quality control processes that enhance product reliability and performance. Additionally, this role requires collaboration with other departments to address quality issues and drive continuous improvement initiatives. Ultimately, the Team Lead will contribute to the overall success of the manufacturing process by ensuring that only the best products are delivered to the market. This is a working lead role. Minimum Qualifications: High school diploma or equivalent; a degree in a related field is preferred. Proven experience in quality inspection

Innovia Medical combines the experience and expertise of Summit Medical, Network Medical, DTR and Eagle Labs to help our medical professional partners elevate the delivery of care to improve patient outcomes. We develop products not just for our customers, but with our customers. Our collaborative approach cultivates innovative medical solutions for the global healthcare industry. Through excellence in design, supply chain management, manufacturing and customer service we put Quality at the forefront in all aspects of our business. Job Summary The Director of Quality is responsible for managing the Quality Management System (QMS) for Summit Medical and Eagle Labs in compliance with the requirements of ISO13485:2016, 21 CFR Part 820, EU MDD, EU MDR and UK MDR. Job Purpose To ensure the respective QMSs and Quality practices remain compliant with appropriate standards and regulations including but not limited to ISO13485:2016, and 21 CFR Part 820. To promote best Quality practice in all a

Position Overview: The Senior Quality Engineer ensures compliance with regulatory requirements (FDA QSR, ISO 13485, ISO 14971) and company procedures, contributing to both development and production teams to meet customer, company, and regulatory standards. The role includes process development, quality support, risk assessments, root cause analysis, and continuous improvement efforts. Key Responsibilities: Ensure adherence to Quality Management System (QMS) and regulatory standards. Provide support to either the Development or Production teams, ensuring product manufacturability, process qualification, and regulatory compliance. Develop, validate, and execute test methods, standard work, and process controls for new and existing products. Conduct risk assessments, quality plans, control plans, and root cause analyses to resolve issues and improve processes. Support process improvement, nonconformance investigations, customer complaints, and supplier quality issues. Lead or participate

Senior Manufacturing Engineer Note: We do not hire C2C Position Summary: The Senior Manufacturing Engineer will design and develop manufacturing processes, tooling, and fixtures to meet daily production schedules while enhancing productivity and product quality. This role involves managing projects that include new production equipment, process improvements, and cost reductions while supporting new product introductions. The ideal candidate must have expertise in process validation, or their resume will be rejected. Essential Functions: Manage projects involving new production equipment, process improvements, and cost reductions. Provide technical mentorship to engineers and technicians. Conduct Process Failure Modes and Effects Analysis (FMEAs) and Process Validations. Improve product quality, labor efficiency, and throughput using Lean manufacturing concepts. Coordinate the design, procurement, build, and debug of tooling, machinery, and test equipment. Work with Product Development

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of . Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high e