10 Permanent ISO 13485 Jobs in Cambridgeshire

manufacturing. Maintain accurate documentation and lab records. Introduce innovative technologies and make informed recommendations. Manage project scopes, resources, and budgets effectively. Ensure compliance with ISO 13485 standards. Requirements: Essential: Bachelor's degree or higher in a biological-related discipline, with significant post-qualification experience. Minimum of 3 years … experience in people management. Proven ability to lead, motivate, and mentor a team of scientists. Thorough understanding of product design control and ISO 13485 regulations. Extensive experience in molecular biology techniques such as FISH, PCR, DNA manipulation, and fluorescent labelling. Previous work in a regulated, diagnostic environment. Strong … software tools such as BLAST/BLAT and sequence searching methods. Comprehensive knowledge of genomic principles and databases. Additional management experience preferred. Experience in ISO 9001 and ISO 13485 compliant environments, including participation in audits. If you are ready to make a significant impact in a research more »

oversight of GMP and compliance within company operations, providing guidance on GMP, GDP and GLP ensuring compliance with internal and external requirements with both ISO 13485 and ISO 9001 standards. Requirements for this role: Degree in relevant biological discipline Significant experience within industry in similar role, within … ISO 13485 and ISO 9001 environments Experience with internal auditing Experience in manufacturing equipment validation Interviews are imminent so please apply now or contact Chris Morris at Science Solutions for more information. more »

software development life cycle experience Microcontrollers (ARM STM32, M-Series, PIC, ESP32 etc.) Linux Non-Essential/Nice to have’s: Medical device standards (ISO13485, IEC 62304 etc.) Wireless technologies (Bluetooth/Wi-Fi etc.) Python/other programming languages Experience in a consultancy/start up environment Benefits: Profit more »

NeuroTech AIMDs. Understands the end-to-end process for Class III Medical Devices. Has worked with contract manufacturers or built an internal manufacturing capability. ISO understanding across ISO 13485 requirements. How do I apply? To apply for this outstanding opportunity, please contact Nathan Sasso at Pivotal via more »

Minimum of 5 years’ experience in developing software and troubleshooting hardware issues. Previous involvement in regulated In Vitro Diagnostic (IVD) development, including operating under ISO13485 and IEC62304. Significant experience in formal software verification Proficiency in C/C++ programming languages. Experience with Real-Time Operating Systems (RTOS) and bare-metal more »

op-amps, inductors etc.) Full product development life cycle experience from concept to release Non-Essential/Nice to have’s: Medical device standards (ISO13485, IEC 62304 etc.) Wireless technologies (Bluetooth/Wi-Fi etc.) Power Electronics Experience in a consultancy/start up environment Benefits: Profit share bonus more »

years’ experience in developing software and bringing regulated products to market. Previous involvement in regulated In Vitro Diagnostic (IVD) development, including operating under ISO13485 and IEC62304. Significant experience in formal software verification Proficiency in C/C++ programming languages. Experience with Real-Time Operating Systems (RTOS) and bare-metal development. more »

. Collaborate with the Engineering, Manufacturing and Biology teams working towards regulatory submission and product launch. Adhere to the requirements of working in an ISO 13485/FDA regulated environment. Experience … and skills required to be successful in this position: Practical experience in verification of In Vitro Diagnostic (IVD) devices or medical devices in an ISO13485/21CFR regulated environment. Previous experience in writing test protocols in line with Product Requirement Specifications. Degree in Science or Engineering or possess equivalent relevant more »

the following areas: Supplier & raw material controls, Process Validation, Equipment (Qualification, SOPs, Software Validation) 🔹 Your qualifications: Strong background in Software Validation Quality Management Systems ISO13485 GMP Experience working with IVD/Medical Devices ✉️ If you are interested in this exciting role, please send your application directly to ahmed@elemed.eu 📲 Would more »

We have an exciting opportunity for an R&D Manager to join a leading genetic research company based in the Cambridgeshire area. As the R&D Manager you will be responsible for managing and resourcing the development team for new more »