Manager, Quality Salary at Dicastal North America Inc BETA

Summary The Manufacturing Supervisor is responsible for supervising operations to ensure production is operating in a safe, efficient, and timely manner. Responsible for productions schedules and posting of daily work assignments based upon production needs and individual strengths. Must be shop floor orientated and provide “hands-on” product/process support for all reports on a daily basis. This individual will be the driver behind product/process safety, quality, delivery and morale. Accountable for continuous improvement of assigned department as well as training and development of direct reports. Job Duties All work must be performed in a safe, efficient manner in compliance with Company Policy, Local, Provincial and/or Federal rules and regulations and if applicable Collective Agreement. Communicates, trains, guides and coaches employees to achieve operational initiatives that optimize team efforts in the manufacturing of high quality products. Evaluates interpersonal skills, prov

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

Quality Manager - Manufacturing Our client is a growing manufacturing company and they are seeking an experienced Quality Manager to lead their quality department and drive continuous improvement initiatives. This role will oversee ISO 9001:2015 compliance, manage quality systems, and support new product launches while fostering a culture of excellence and collaboration. What You'll Do: Lead and develop the quality team, ensuring strong performance and professional growth. Maintain and improve quality control and document management systems to meet industry standards. Drive continuous improvement initiatives, root cause analysis, and corrective action plans. Support new product launches, overseeing APQP, PPAP, and validation processes. Collaborate with cross-functional teams to enhance quality standards and production efficiency. Implement data-driven quality systems, ensuring accurate tracking and reporting. What You Bring: 7+ years of experience in a manufacturing environment, with a

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

Summary The Manufacturing Supervisor is responsible for supervising operations to ensure production is operating in a safe, efficient, and timely manner. Responsible for productions schedules and posting of daily work assignments based upon production needs and individual strengths. Must be shop floor orientated and provide “hands-on” product/process support for all reports on a daily basis. This individual will be the driver behind product/process safety, quality, delivery and morale. Accountable for continuous improvement of assigned department as well as training and development of direct reports. Job Duties All work must be performed in a safe, efficient manner in compliance with Company Policy, Local, Provincial and/or Federal rules and regulations and if applicable Collective Agreement. Communicates, trains, guides and coaches employees to achieve operational initiatives that optimize team efforts in the manufacturing of high quality products. Evaluates interpersonal skills, prov

Summary The Manufacturing Supervisor is responsible for supervising operations to ensure production is operating in a safe, efficient, and timely manner. Responsible for productions schedules and posting of daily work assignments based upon production needs and individual strengths. Must be shop floor orientated and provide “hands-on” product/process support for all reports on a daily basis. This individual will be the driver behind product/process safety, quality, delivery and morale. Accountable for continuous improvement of assigned department as well as training and development of direct reports. Job Duties All work must be performed in a safe, efficient manner in compliance with Company Policy, Local, Provincial and/or Federal rules and regulations and if applicable Collective Agreement. Communicates, trains, guides and coaches employees to achieve operational initiatives that optimize team efforts in the manufacturing of high quality products. Evaluates interpersonal skills, prov