Manager, Quality Salary at Tarmac Llc BETA

Join a dynamic team where your expertise in food safety and quality will drive innovation and excellence in a collaborative and supportive environment. Qualifications Proven Leadership: Minimum of 5 years of management experience in food safety and quality within a high-risk environment. Educational Background: Bachelor's degree in Food Safety, Microbiology, Chemistry, Food Science, Engineering, or a related field. Industry Experience: Over 5 years in food processing, including at least 2 years in a manufacturing environment under USDA and/or FDA regulations. Responsibilities Compliance Management: Ensure adherence to FDA requirements and oversee plant compliance with regulatory bodies. Quality Assurance Integration: Lead the integration of quality assurance and food safety processes to align with business objectives, including certifications and audits. Team Leadership: Develop and coach a high-performance team, focusing on communication, development, and succession planning. Benefits

Job Description Job Description Hemostasis, LLC designs, develops, manufactures, and markets advanced hemostat, wound healing technologies, and advanced medical devices for use in the healthcare industry. Our business is growing and we are seeking a Manufacturing / Process Development Engineer to support our increasing demand and implementation of new medical device products to market. The qualified candidate will provide a leadership role in identifying and implementing improvements across several product manufacturing areas as well as provide a supporting role in manufacturing transfer projects. This role will interface in a collaborative team-based environment with research & development, operations, quality, regulatory, sales, and marketing teams to support and drive the successful implementation & launch of new medical devices. There is a great amount of growth opportunity within the organization and the right candidate will have exposure to a large variety of internally manufactu

A medical device manufacturing client is looking to hire a Quality Technician to join their engineering team! This person needs to be able to work Monday through Thursday, 3:30 PM until 2 AM, 100% onsite in Eden Prairie. This direct hire employee will perform materials and product assessment testing in support of medical device development and manufacturing in compliance with GMP. This individual is responsible for receiving and in-process inspections, material release in support of medical device manufacturing. This Quality Technician may be called upon for reviewing and approving job travelers prior to product release and should have experience supporting administration of quality systems within the electronic QMS. Must Haves: At least 2 years of relevant medical device/ISO 13485 experience Knowledge and experience with electronics manufacturing Knowledge of quality systems including use of electronic quality management systems software Knowledge of electrical and mechanical testing

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

Job Description Job Description BIOLYPH is seeking an experienced, team-oriented, and responsive Quality Systems Manager. This full-time position offers your choice of a 4 or 5 day work week, competitive benefits, growth opportunities, and a culture of life-work balance. The Quality Systems Manager is primarily responsible for developing, implementing, and monitoring the required sub-systems of BIOLYPH’s Quality Management System (QMS). In doing this, they serve as the back-up Quality System Representative and help monitor the health of the QMS. This will be done in alignment with BIOLYPH’s business model of producing our Clients’ IVD/RUO products Effectively, Efficiently, and Economically. Essential Functions: Quality Management System: Implement and maintain all necessary systems and procedures to satisfy applicable regulations and/or expressed Client needs Analyze quality data and provide insights for decision-making and continuous improvement projects Work closely with cross-functi

Russell Tobin has an Instrumentation Engineer opening in Mendota Heights, MN. This is a direct-hire position! Shift: 1st on-site Compensation $85,000-160,00/year based on experience Relocation will be considered. Work includes support for all project phases, with particular focus in front-end engineering and detailed engineering. Position will be assigned as the instrumentation and controls engineering lead for projects and will be responsible for coordination and ensuring effective communication with other engineering disciplines Responsibilities Responsible for preparing instruments and control system specifications, instrument data sheets Responsible for review of instrument and control systems vendor drawings and data. Interface with suppliers, clients, other engineering disciplines, and designers. Participates in the development of P&IDs, equipment/material specifications, logic diagrams, cause & effect diagrams, control narratives, functional specifications and related instrument

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

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. 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 employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a g