Average Development Scientist salary in Cambridge

The Senior Product/Process Development Scientist will play a pivotal role in advancing our mission to make healthcare more accessible and effective through innovative Point of Care (PoC) diagnostic solutions. This position is ideal for a driven scientist with a strong background in diagnostics or medical devices who thrives on optimizing processes, leading product enhancements, and collaborating across teams. Key Responsibilities: Process Analysis & Optimization: Conduct detailed evaluations of existing manufacturing processes to identify bottlenecks and areas for improvement. Develop and implement upgrades to enhance efficiency, reduce costs, and boost product quality. Product Performance Enhancement: Assess current products for performance, quality, and user satisfaction, implementing strategic upgrades that align with user needs and regulatory standards. Research & Development: Innovate and develop new methodologies or technologies for product and process improvement. You'll be at the forefront of R&D initiatives, bringing new ideas to enhance product functionality and scalability. Data-Driven Decision Making: Collect, analyze, and interpret data to track performance metrics, support process improvements, and measure the impact of product changes. Cross-Functional Collaboration: Collaborate closely with engineering, manufacturing, and quality assurance teams to implement and validate process changes. Ensure alignment of all improvements with company goals and customer needs. Testing & Validation: Design and execute experiments for new processes and product modifications. Conduct validation studies to ensure modifications meet rigorous performance and compliance standards. Documentation & Reporting: Maintain comprehensive records of research, methodologies, and findings. Prepare reports to communicate results and recommendations to stakeholders. Training & Support: Support and train team members on new processes, methodologies, and product updates, fostering knowledge-sharing and smooth transitions. Regulatory Compliance: Ensure that all process and product improvements comply with industry standards and regulations, including ISO 13485, IVDD, and IVDR. Continuous Improvement Initiatives: Lead and participate in projects that promote ongoing improvement in product quality and process efficiency, contributing to a culture of innovation and growth. Qualifications & Experience: Educational Background: Degree in Chemistry, Life Sciences, or a related field. Knowledge of surface chemistry is a plus. Industry Experience: 5+ years in manufacturing for diagnostics or medical devices, with a focus on PoC diagnostics or lateral flow devices. Technical Expertise: Strong knowledge in microfluidics, immunoassays, and affinity/colorimetric sensing systems. Familiarity with handling biomolecules, such as proteins, antibodies, and metabolites. Regulatory Knowledge: Proficiency with quality systems (ISO 13485) and understanding of in-vitro diagnostic regulations (IVDD, IVDR). Tech Transfer: At least 3 years of experience in transferring technology from R&D to production, with a demonstrated ability to adapt laboratory processes for scalable manufacturing. Soft Skills: Excellent communication skills, ability to work effectively within cross-functional teams, and a proactive, organized approach to problem-solving. This role provides a unique opportunity to join a growing start-up at an exciting stage of development. If you're passionate about making a tangible impact in healthcare, let's discuss how your experience can help us reach new heights in diagnostic innovation. To learn more or apply, contact me at: ?? ??

Downstream Process Development Scientist Location - Cambridge Sector - Biotechnology Salary- £28,000 - £35,000 (depending on interview performance & experience) Full time, permanent role Do you have experience in chromatographic process development (e.g. with AKTA systems)? Do you have hands on experience in downstream processing within a biotech setting? We have an exciting opportunity available with a biotechnology company in Cambridge. Our client is looking to onboard an experienced scientist with prior R&D experience who can hit the ground running in a process development role. Applicants must have current UK work eligibility. The Role As a scientist within the downstream process development team, you will be responsible for: Developing and optimising processes to ensure the successful manufacturing of DNA products,Scaling up R&D downstream processes into larger scale manufacturing,Maintaining QMS documentation and creating / updating SOPs,Independently carrying out experimental troubleshooting. Skills and Experience Needed The ideal candidate will have the following: At least 1-2 years of relevant downstream processing experience within a biotech / R&D setting (essential).Experience with chromatographic process development using AKTA systems (essential).Comfortable working independently with AKTA Pure / Avant or Tangential Flow Filtration (TFF) (essential).Existing UK work eligibility (essential).Hands on experience or knowledge of working in compliance with GMP regulations (essential).Experience with tech transfer of chromatographic processes from R&D to GMP / Analytics (desirable).Comfortable working within a QMS and writing / updating SOPs (desirable).Experience working with Design of Experiments (DoE) software (desirable). The Package As an up-and-coming Cambridge Biotech, our client can offer a competitive salary and benefits package including private pension and private health insurance.

Production Scientist - IVD Cambridge Permanent £ Competitive depending on skills, background and experience Role profile: This is a newly created role working for a flourishing biotech organisation based near to Cambridge, UK. You will report to the Senior Production Scientist and support with key duties in the manufacture and QC of specialist reagents. Core duties: Preparation of reagents, lyophilisation and quality control and production of small-medium scale batches.Handling receipt of reagents and chemicals -including aliquoting, storage and uploading onto the QMS as necessary.Working alongside CMO's and in-house specialists to support the production scaling activities.Create and implement QC and validation protocols, ensuring that regulatory processes are followed meticulously.Report any QC pass and fails, monitoring any non-conformance closely and taking corrective action.Strictly adhere to all ISO 13485/FDA regulations.Follow SOP's, maintaining accurate records and document all production activities in accordance with company policy. Your background: BSc or equivalent in a Biological discipline (or related).Background in an IVD development setting, working to ISO 13485 standards in a production or QC team.Proven industry/commercial lab experience, ideally where there are devices in development.Good proficiency with RT-PCR along with other classic molecular skills such as reagent and/or chemical handling.Must have a good command of operating within a QMS.Exemplary attention to detail, methodical approach and accustomed to working in a busy and demanding environment.Strong communication and organisational skills; able to collaborate well within a multidisciplinary environment. Does this sound like you? Apply here by attaching your CV in Word or reach out for more information. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.