We are aware of a global phishing scam with employees from companies impersonated across email, WhatsApp, and Telegram.We are confident that no PageGroup system has been breached. Find out how to protect yourself and the signs to look out for
Browse our jobs and apply for your next role.
Reach out to us or discover some great insights that could help you fill your next vacancy.
PageGroup changes lives for people through creating opportunity to reach potential.
We find the best talent for our clients and match candidates to their ideal jobs.
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 Assurance Engineer will play a pivotal role in ensuring top-notch hardware, software, and process quality throughout the product life cycle. This dynamic role involves developing and implementing cutting-edge quality initiatives and delivering results that surpass industry standards while continuously championing customer satisfaction and regulatory compliance.
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.
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.
Making sure componenet and finished products and proccesses are approved. Leading MRB activities.
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 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.
Create Job alert to receive Quality Technical Essex jobs via email the minute they become available
Submit your resume to register with us and we will contact you if a suitable role becomes available