1 to 2 of 2 Permanent Market Surveillance Jobs in the South East

which has a focus on quality, compliance and ISO standards. [ The role ] Leading and project managing the entire product development process from concept to market launch. Sourcing products from suppliers to ensure suitability Ensuring compliance with all relevant regulations and standards for medical devices. Collaborating with cross-functional teams … including R&D, marketing, and quality assurance to develop and enhance products. Conducting market research to identify new opportunities and improvements for existing products. Developing and maintaining product documentation, including technical files and submissions. Providing regulatory guidance and support to internal teams and external partners. Monitoring and interpreting regulatory … changes to ensure company products remain compliant. Managing product lifecycle and post-market surveillance activities. Requirements Bachelors degree in Engineering, Life Sciences, or a related field would be advantageous but not essential Extensive experience in product development and sourcing relevant products Excellent project management and organisational skills Ability more »

IVD Directive (98/79/EC). Lead strategies for a large product portfolio including supporting new registrations, authoring technical files, and post-market surveillance. A minimum of 8 years post-qualification experience in regulatory affairs in the medical device and/or pharmaceutical industry in product registration more »