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The Quality Systems Engineer at plays a crucial role in developing and maintaining quality systems, ensuring compliance with industry standards and driving continuous improvement. They are responsible for implementing quality processes, conducting audits, and leading corrective actions to enhance overall product quality and customer satisfaction.
This role involves overseeing and managing the quality management system (QMS) to ensure compliance with regulatory standards and company requirements. Responsibilities include developing, implementing, and maintaining QMS processes, conducting audits, and driving continuous improvement initiatives.
This individual will be involved in overseeing and managing the analytical laboratory operations to support product development, reliability and quality assurance activities. Key responsibilities include managing lab resources, developing analytical methods, conducting tests, analyzing data, and ensuring compliance with quality standards and regulations.
Reporting into the General manager, The Director of Quality & Regulatory will direct the organisation's Regulatory Affairs and Quality Assurance functions in multiple areas including documentation, compliance, audits and regulatory submissions.
The quality engineer would be responsible for maintaining and continuously improving the Quality Management System (QMS) resulting in improved: safety, quality compliance, procedures, and processes. The quality engineer will report directly to the Quality Manager but will work closely and collaborate with all their peers on the management team and all employees. The quality engineer may also support inspection personnel when needed.
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 Engineer will join a dynamic aerospace manufacturing company responsible for maintaining and supporting the production of composite components for military contracts, including the US 60 Black Hawk helicopter. Manage Quality Management System (QMS) operations, internal audits, and root cause/corrective actions to ensure adherence to AS9100 standards and timely delivery of high-quality products.
The Supplier Quality Engineer will oversee the delivery of quality parts, components, and materials from suppliers, ensuring adherence to company standards. They will manage supplier selection and qualification, monitor component quality throughout the manufacturing cycle, and resolve any supplier-related issues, collaborating with internal design teams and suppliers during the component qualification process.
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 position with my client involves ensuring compliance with medical device regulations, particularly ISO 13485 and FDA standards, to maintain the highest quality standards in organ preservation and transplantation technologies. The role requires proactive problem-solving, collaboration with cross-functional teams, and a commitment to continuous improvement to uphold my clients' mission of advancing organ transplantation technology.
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.
A Quality Engineer will be responsible for ensuring product quality by applying statistical analysis and quality control methodologies in precision manufacturing. This candidate will collaborate with cross-functional teams to address and prevent quality issues, emphasizing continuous improvement and adherence to high-quality standards.
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.
As the Manufacturing Quality Engineer, you will be responsible for ensuring compliance with quality standards and regulations, conducting audits, and implementing effective quality management systems. You will play a vital role in driving continuous improvement and contributing to the company's cutting-edge technological advancements. The role will also have a heavy focus in aerospace.
Maintain and support production, work with the inspectors, make sure the production parts keep moving. Wear many hats and be able to move at a fast pace.
Making sure componenet and finished products and proccesses are approved. Leading MRB activities.
I am actively looking for a Quality Systems Compliance Specialist to join and help lead continuous improvement initiatives to the quality system.
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.
You will participate in selecting and qualifying suppliers and ensure that they deliver quality parts, components, and materials. You will also be evaluating suppliers' internal functions.
In this role you will be in charge of overseeing and managing quality control processes related to product design. You will ensure compliance with regulatory standards, conducting risk assessments, and leading cross-functional teams in the development and implementation of quality management systems.
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.
In this role you will focus on maintaining and improving product quality within the manufacturing process. Responsibilities include assisting in developing and implementing quality management systems, conducting risk assessments, and collaborating with cross-functional teams to address quality issues and drive continuous improvement.
In this role you will be overseeing and implementing quality control processes to ensure compliance with regulatory standards and maintain product excellence. Responsibilities include developing and implementing quality management systems, conducting risk assessments, and collaborating with cross-functional teams to address quality issues and drive continuous improvement.
Address quality process gaps, training needs, and performance issues in alignment with business goals, while ensuring effective communication with suppliers and customers for timely issue resolution.Collaborate internally to enhance quality systems, identify improvement areas, and achieve top-tier customer service.
This position is a highly visible and dynamic role with exponential growth opportunity. They are looking for individuals with ISO9001 & ISO13485, leadership and customer facing experience to help them in revamping their quality department.
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.
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.
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