Manager, Quality Salary at Pjf Inc BETA

Overview: Our growing company is seeking to hire a Quality Manager for our Byron Center Michigan facilities. This is an incredible opportunity to work with a world class team! In this role, you will provide leadership of MECs Quality Systems and team. This is a great position for a change agent who has passion for driving quality improvements to achieve the highest level of customer satisfaction. MECs Quality Manager will take an active role in leading the Quality Engineering activities that meet and exceed our customer requirements. Responsibilities: Lead and support the activities of the Performance Structures Division in the development and improvement of MEC Quality Management system that meets IATF16949 requirements Plan, develop, implement, train, and assess the effectiveness of MECs quality systems to improve internal and outgoing product quality that will achieve higher levels of customer satisfaction. Interact with all functional areas in the company to assure seamless process

Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day. Overview of this Position: The Quality Assurance Specialist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. The Quality Assurance Specialist provides oversight and general support for the manufacturing of aseptic processes, deviation and CAPA systems, batch record review, SOP creation and revision, review of quality documents, and supports the Quality Management System. Non-Negotiable Requirements: •Bachelor's degree in Life Sciences or related field, and 2-5 years related work experienc

About the Organization RENK America is a leading supplier in the defense, marine and industry sector with superior mobility, propulsion and drive train solutions. Our tradition is centered on precision-engineered systems for maximum impact, efficiency and endurance. RENK's ambition is to support each and every one of its customers to exceed standards in harsh conditions and combat situations. RENK America employs over 500 employees at our US locations in Muskegon, Michigan, Cincinnati, Ohio, Camby, Indiana and Roseville, Michigan. RENK America is driven by this sense of pride and purpose in our country and our community. Description The Supplier Quality Specialist (SQA) is responsible for driving quality for assigned suppliers, including quality plan implementation. As a key member of the Source Selection team, the SQA evaluates, selects, develops and qualifies suppliers, and drives continuous improvement utilizing supplier scorecards, supplier audits, and improvement plans where neede

Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day. Overview of this Position: The Quality Assurance Specialist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. The Quality Assurance Specialist provides oversight and general support for the manufacturing of aseptic processes, deviation and CAPA systems, batch record review, SOP creation and revision, review of quality documents, and supports the Quality Management System. Non-Negotiable Requirements: •Bachelor's degree in Life Sciences or related field, and 2-5 years related work experienc

Join a team that improves patient outcomes, through innovative and flexible solutions to the acute care market! When you work for Skytron, you get so much more than a job, including: Comprehensive benefits package, beginning on day one Annual Pool Bonus Paid vacation, personal days, and holidays 401(k) and Profit sharing Tuition reimbursement program Onsite gym Family-owned and operated business As the Quality Assurance Specialist, you will: Facilitate the investigation and closure of complaints Facilitate and close internal and supplier corrective action reports Work with Skytron's internal audit team to schedule and execute audits, report findings, and ensure any resulting corrective actions are appropriately implemented Initiate nonconforming product process, according to established procedures Assist in the management of recalls and field corrections, ensuring timelines are met and activities are properly documented Maintain document control within the Quality Management System Per

Join BAMF Health, where you're not just part of a team; you're at the forefront of a revolution in Theranostics, changing lives for the better. As a member of our global team, you'll contribute to pioneering technology and deliver top-tier patient care. Located in the heart of downtown Grand Rapids, our cutting-edge global headquarters resides within the state-of-the-art Doug Meijer Medical Innovation Building. Step into our modern and spacious facilities, where innovation thrives and collaboration knows no bounds. Join us in our mission to make Theranostics accessible and affordable for all, and be part of something truly remarkable at BAMF Health. The Quality Assurance Specialist is responsible for providing oversight and general support to the manufacturing/production of radiopharmaceuticals, deviation and CAPA systems, batch record review, SOP creation and revision, review of quality documents, and supports the Quality Management System. Duties and Responsibilities, including but n

Description Autocam Medical is a global contract manufacturer of orthopedic implants, spinal implants, precision instruments and orthopedic cutting tools. We offer a value-added approach to high-precision manufacturing, with specialties in CNC milling, turning and cutter grinding. We are seeking a Quality Manager with a passion to make a meaningful contribution to the medical device industry. Reporting to the Director of Quality and the Site General Manager, the Quality Manager is responsible for developing and maintaining a quality system that ensures all products meet customer specifications and comply with ISO 13485 and regulatory requirements. This role aims to achieve superior quality, reliability, and value for customers while providing guidance and leadership to meet quality goals. The manager will promote the Autocam Medical Production System and uphold the company's high standards for quality and continuous improvement. Responsibilities Provide leadership, direction, and mento

Overview: Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive. Position Summary: Versiti was founded with the belief that together, our blood