ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
Plum Personnel
West Molesey
REGULATORY QUALITY MANAGER SALARY CIRCA £50K DOE HERSHAM About the role Our Client is a highly successful leader in their field who have been trading for over 30 years and looking to maintain that status with an exciting and challenging growth plan for the next 5 years. With a mix of own label and branded products, they sell to c2000 customer
Job Source: Plum PersonnelMeet
united kingdom
Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device Associate Main Purpose of Job and Objectives: Perform Regulatory tasks to ensure compliance with regulations. Prepare regulatory documentation and submissions for product approvals. Develop regulatory plans/strategies for new products and changes to existing produ
Job Source: MeetMeet
London
Job Description I am seeking a highly motivated and experienced Regulatory Affairs Specialist with expertise within OTC/Cosmetics experience to join us on a contracted basis for a period of 6 to 12 months. As a key member of the Regulatory Affairs team, you will play a crucial role in ensuring our products comply with all relevant regulations and
Job Source: MeetLife Science People
London
Job DescriptionTitle: Senior Regulatory Affairs Specialist Location: London Hybrid working Purpose of Job:Support the business with regulatory advice and activities to ensure that timely approval and maintenance activities are carried out on time, that all Regulatory and Quality systems are updated and correct, to identify and flag any potential/ac
Job Source: Life Science PeopleMeet
united kingdom
I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers. They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company in the pharmaceutical industry..... Position Overvi
Job Source: MeetMedicareplus International Ltd
Wembley
Job Description Job Summary RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities · Responsible for maintaining
Job Source: Medicareplus International LtdMeet
London
I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers. They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company in the pharmaceutical industry..... Position Overvie
Job Source: MeetApsida Life Science
united kingdom
Regulatory Affairs Specialist - Lifecycle Maintenance Location: Remote We are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and en
Job Source: Apsida Life ScienceLondon
TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives.
Quality and Regulatory Specialist
As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking solutions in global diagnostics. Your key responsibilities will include document control and the ability to implement robust document control processes while working closely with the Head of Quality and Regulatory Affairs establish the QMS aligned with ISO 13485 requirements, driving continuous improvement and operation excellence.
The successful candidate will also compile technical files with comprehensive documentation to support regulatory submission and product certification while conducting risk management activities in accordance with ISO 14971, identifying potential hazards, assessing risks and implementing effective mitigation strategies.
Quality and Regulatory Specialist Key Responsibilities:
Manage and organize quality and regulatory documentation
Ensure timely and accurate filing per industry standards
Maintain compliance with regulatory requirements
Collaborate with teams for regulatory compliance training
Implement robust document control processes
Maintain compliance throughout the product lifecycle
Assist with the development of comprehensive technical files for CE marking
Collaborate with stakeholders to establish a QMS
Quality and Regulatory Specialist Requirements:
Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences, Regulatory Affairs)
2 years' experience in quality and regulatory affairs within the medical device industry, preferably with exposure to software (IEC 62304) and Software as a Medical Device (SaMD)
Strong understanding of ISO 13485, ISO 14971, and other relevant regulatory standards
Excellent communication skills with the ability to collaborate effectively across multidisciplinary teams
Detail-oriented mindset with a commitment to maintaining the highest standards of quality and compliance
Experience with CE marking processes and regulatory submissions is highly desirable
This is an exciting opportunity to be part of a dynamic and innovative company dedicated to making a meaningful impact on the lives of millions affected by diabetes. If you are driven by excellence, passionate about regulatory compliance, and eager to contribute to the future of healthcare, the Head of Quality and Regulatory Affairs is driven to help you develop your career with a clear pathway set to develop up to a managerial level.
If you're interested, please apply with an up to date CV as this role will not be available for long.
Quality & Regulatory Specialist jobs in London
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.