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The Engineering Manager will be an integral leader at my client's manufacturing shop near Brookfield, managing production from customer contact all the way to final product. This role will report directly to the President and will be heavily involved in organizational decision making.
The Quality Systems Manager for this client oversees all aspects of quality management systems, ensuring compliance with regulatory standards such as ISO and coordinating internal and external audits. They drive continuous improvement initiatives, manage corrective and preventive actions, and foster a culture of quality excellence throughout the organization.
The Quality Systems Manager oversees all aspects of the organization's quality management and improvement efforts, ensuring compliance with relevant standards and regulations such as ISO 9001, IATF 16949, AS9100D, and ISO 13485, while also driving continuous improvement and adherence to customer requirements. They act as the Management Representative for QMS, coordinating internal audits, external assessments, and corrective/preventive actions.
The Quality Engineer 3 position with my client involves ensuring adherence to quality standards and regulatory requirements in the production of medical devices and pharmaceutical products. Responsibilities include conducting quality assessments, implementing corrective actions, and collaborating cross-functionally to drive continuous improvement in product quality and reliability.
Step into the role of Senior Quality Assurance Specialist, where you'll leverage your extensive experience to ensure adherence to the highest quality standards and regulatory compliance within the dynamic field of medical devices. As a key player, you'll spearhead initiatives aimed at driving innovation and advancing patient care through meticulous attention to detail and a commitment to excellence.
Making sure componenet and finished products and proccesses are approved. Leading MRB activities.
In this role you will be focused on ensuring the quality and regulatory compliance of product designs. Responsibilities may include overseeing design control processes, conducting risk assessments, and collaborating with cross-functional teams to develop and implement quality management systems.
The Senior Quality Engineer will enhance awareness, visibility, and communication regarding quality initiatives while supporting departmental, functional, and corporate quality goals within a medical device manufacturing space. The ideal candidate will possess a robust understanding of FDA/ISO 13485 Quality System requirements, GxP standards, and other pertinent regulations.
Your role as a Quality ambassador in the Specialty Products division is centered on boosting awareness, visibility, and communication regarding quality, with a particular focus on aligning these efforts with the division's unique needs and objectives.
The Design Quality Engineer role involves ensuring the quality and compliance of medical device designs, particularly in organ preservation and transplantation. Candidates will apply expertise in quality management systems and regulatory standards to drive product safety and efficacy in this critical healthcare field.
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