CY Partners

Test Engineer Diagnostics / Medical Devices Permanent, Full-Time Based in Bristol £ Competitive salary + Benefits Are you a hands-on Engineer with a passion for testing and validating complex diagnostic systems? Would you like to play a key role in developing next-generation molecular diagnostics with real-world clinical impact? My client is a pioneering biotech organisation developing cutting-edge diagnostic technologies that combine machine learning, DNA sequencing, and advanced engineering to revolutionise the detection of disease. As part of their continued growth, they are looking to bring onboard a Test Engineer to support the integration, testing, and optimisation of highly specialised instrumentation within their R&D team. Working in close collaboration with engineers and scientists across disciplines, you ll contribute directly to the validation and verification of novel medical technologies - ensuring high performance, reliability, and compliance across every stage of product development. Key Responsibilities of the Test Engineer Diagnostics / Medical Devices will include: Testing complex instrument systems including electromechanical, software, thermal, and optical subsystems. Developing and optimising test protocols in collaboration with mechanical and manufacturing engineers. Providing technical insights and feedback from testing to guide design decisions and product improvements. Collaborating cross-functionally to drive verification and validation (V&V), troubleshooting and design control activities. Building, troubleshooting, and maintaining specialised instrumentation, including deployment and support at partner sites. Managing and delivering your own projects from concept through to completion. Supporting the implementation of ISO 13485 compliant quality processes. Drafting and maintaining detailed test documentation, procedures, and reports. To be considered for the Test Engineer Diagnostics / Medical Devices role, you ll need: BEng / MEng / PhD in a relevant discipline (e.g. Engineering, Biomedical Engineering, Physics etc.) or equivalent working experience. Hands-on experience with testing and validation of complex systems e.g. combining fluidic, mechanical, optical, and thermal subsystems. Proven experience working on complex medical diagnostic systems or related electromechanical instruments. Proven ability to design and execute verification and validation (V&V) test plans and author associated SOPs. Skilled in interpreting technical drawings, circuit diagrams, and design documentation. Strong proficiency with CAD software (e.g. Fusion360, SolidWorks). Clear communication skills with the ability to present technical findings to varied stakeholders. Highly organised, self-driven, and adaptable to dynamic, fast-paced R&D environments. Beneficial: Experience within the Medical Device, Biotechnology or Life Sciences sectors. Experience testing and maintaining early prototype stage systems. Experience developing products under Design Controls within an ISO 13485 or ISO 14971 compliant environment. Whether you re currently working in test and verification within MedTech or looking to step into a role with greater technical variety, this Bristol-based opportunity offers a chance to be part of a growing, mission-driven organisation creating life-saving diagnostic solutions. For further information, please apply online or contact Katie-May Kress at CY Partners for further information. Key Words: Test Engineer, Validation Engineer, Systems Engineer, Instrumentation, Electromechanical, Diagnostics, Medical Devices, IVD, Biotech, V&V, Verification and Validation, ISO 13485, Design Controls, CAD, Fusion360, SolidWorks, Fluidics, Optical Systems, DNA Sequencing, Biosensing, Biotechnology, Bristol The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

Microfluidics Engineer IVD / Diagnostics Permanent, Full-Time Based in Bristol £ Competitive salary + Benefits Are you a Microfluidics Engineer with a passion for developing innovative diagnostic technologies? Would you like to play a key role in bringing life-saving molecular diagnostics closer to patients? My client is a pioneering biotech organisation developing next-generation diagnostic solutions that harness DNA sequencing and machine learning to rapidly detect disease. As they continue to expand, they re looking to bring onboard an experienced Microfluidics Engineer to design, prototype, and optimise advanced microfluidic systems that form the core of their cutting-edge diagnostic platform. Working within a multidisciplinary team of engineers and scientists, this is a hands-on opportunity to apply your technical creativity to real-world medical challenges - from concept through to device fabrication and performance validation. Key Responsibilities of the Microfluidics Engineer IVD / Diagnostics will include: Designing and developing microfluidic systems for diagnostic applications, using CAD software, fabrication methods and test equipment. Fabricating microfluidic devices using techniques such as laser micromachining, CNC machining, 3D printing, and diffusion bonding. Building test rigs to optimise and enhance device performance. Conducting experiments to validate and improve microfluidic systems. Collaborating with scientists and engineers to integrate fluidic systems with other diagnostic technologies. Managing projects from concept to completion, delivering robust technical outcomes in a fast-paced R&D environment. Maintaining accurate documentation in line with internal quality and ISO 13485 standards. To be considered for the Microfluidics Engineer IVD / Diagnostics position, you ll need: PhD / MSc in a relevant discipline (e.g. Engineering, Biomedical Engineering, Physics etc.) or equivalent working experience. Proven experience within microfluidics, including design, fabrication and testing of microfluidic systems. Engineering experience gained within industry, in particular within Medical Devices / Diagnostics / Biotech would be advantageous. Strong proficiency in CAD software such as Fusion360 or SolidWorks. Ability to independently plan, execute, and communicate experimental work and project outcomes. Excellent communication skills and a proactive, adaptable approach to problem-solving. Beneficial: Experience with fluidic systems, electrical circuit design and robotics. Knowledge of molecular biology, Next Generation Sequencing (NGS), or genomics. Programming experience (e.g. Python). Experience working under Design Controls in an ISO 13485 environment. Whether you re currently in industry or transitioning from academia, this Bristol-based opportunity offers the chance to apply your microfluidics expertise to truly impactful healthcare innovation. For further information, please apply online or contact Katie-May Kress at CY Partners for further information. Key Words: Microfluidics, Microfluidic Engineer, Diagnostics, Med Tech, Medical Device, Biotech, Lab-on-a-Chip, Fluidics, CAD, Fusion360, SolidWorks, Device Fabrication, R&D, Biosensing, Point-of-Care, Instrumentation, DNA Sequencing, ISO 13485, Biotechnology, Molecular Diagnostics, Bristol The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

Warehouse Operator Location: Harlow Contract Length: 12 Months Pay Rate: £15.00 CY Partners are recruiting for a Warehouse Operator to join a global pharmaceutical manufacturer based at their site in Harlow. Here you'll play a key role in receiving, warehousing, sampling, dispensing, picking, packing, and shipping materials that support global clinical studies. This hands-on role ensures timely and compliant supply of clinical trial materials and investigational products. What you ll do: Execute end-to-end logistics operations to cGxP standards Support pilot plant, packaging ops, clinical sites & depots Collaborate cross-functionally to meet patient supply needs Contribute to safety, compliance, audit readiness, and process improvement Flex across roles to support capacity and business continuity What you ll need: Knowledge of logistics systems (e.g., Comet, Xpress) Understanding of cGxP and SOP compliance Strong communication and prioritisation skills Awareness of cross-border shipping & cold chain processes A proactive, detail-oriented, team-focused mindset If this role sounds interesting to you apply now with a copy of your CV or email (url removed) with any questions.

CY Partners are working with a leading UK research organisation, based in York, who specialise in environmental science. They re seeking an experienced Senior Scientist to join their Animal Health Monitoring team In this position, you ll take ownership of scientific delivery, contribute to new project development within a highly regarded organisation known for its technical excellence. Key Responsibilities: Lead and deliver high-quality diagnostic and screening services in animal health monitoring, ensuring projects are completed accurately, efficiently and to strict timelines. Oversee and support scientists and assistant scientists, ensuring adherence to quality systems, licensing requirements, and health & safety standards. Contribute to the development of new proposals, products, and service improvements. Engage in scientific publication, presentation and collaboration opportunities to enhance both your own and the organisation s scientific reputation. Requirements: Degree-qualified (BSc or higher) in a relevant biological or veterinary science discipline, with significant experience in veterinary diagnostics. Strong technical expertise across areas such as molecular diagnostics, bacteriology, parasitology, serology, and necropsy. Strong understanding of quality standards, H&S requirements, and regulatory frameworks (including FELASA recommendations). Excellent organisational and communication skills, with the ability to manage multiple projects, report effectively, and represent your work at meetings or conferences. This is an exciting opportunity for a driven Scientist who wants to take ownership of impactful animal health research within a highly respected organisation. If you re ready to apply today, get in touch with Graham at CY Partners to discuss.

QC Analyst Location: Worthing, West Sussex Salary: £15.64 p/h Employment Type: 6 Month Contract CY Partners have an exciting contract opportunity for a QC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment. This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products. Key Responsibilities: Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards. Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques. Calibrate, verify, and maintain analytical instruments and systems. Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP. Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed. Contribute to the validation of analytical methods and equipment. About You: You ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry. Requirements: HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline. Proven experience in a GMP-regulated lab, with hands-on experience using HPLC. Strong documentation and data reporting skills. Detail-oriented, methodical, and safety-conscious. Able to communicate clearly and work effectively as part of a multidisciplinary team. A proactive, flexible approach to working in a fast-moving manufacturing environment. Whether you re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.