CY Partners

Senior Scientist Bioanalysis Permanent Position Paying up to £48,000 + Bonus + Benefits Based in North London Are you an experienced scientist with expertise in bioanalytical methods, with a particular focus on plate based assays e.g. ELISA? Would you like to work within the Research and Development (R&D) team of a reputable scientific organisation, making a direct difference to patients lives across the globe? My client, a leader in delivering high quality, biological pharmaceutical products is seeking a Senior Scientist Bioanalysis to join their successful R&D team in London. In this role you will lead R&D projects focused on advancing biological therapies, whilst also providing technical expertise and managing a small team of scientists. This is an exciting opportunity to join a knowledgeable team of scientists striving to make a positive and long lasting impact on patients lives across the globe. Key Responsibilities of the Senior Scientist Bioanalysis include: Lead Research and Development projects through acting as the project lead and point of contact. Deliver R&D projects in line with agreed timelines, updating internal and external stakeholders on study progress. Develop and optimise Bioanalytical methods. Design, execute and analyse experiments in line with R&D deliverables. Act as a technical expert within Bioanalysis, providing guidance and advice to colleagues as needed. Manage a small team of scientists, identifying development opportunities and driving career progression. Ensure compliance with Health and Safety guidelines, SOP s and regulatory requirements e.g. GLP and GMP. Accurately record and present scientific results through the completion of laboratory records, written reports and presentations. To be considered for the Senior Scientist Bioanalysis , you will need the following skills and experience; PhD, MSc or BSc in a relevant life science discipline e.g. Biochemistry, Biological Science, Molecular Biology etc., or equivalent working experience. Significant experience with bioanalytical methods e.g. plate based assays such as ELISA, gel electrophoresis, SDS-Page, protein analysers etc. including method optimisation and development. Strong foundation of scientific knowledge across protein purification and characterisation / analysis methods. Prior experience in managing and/or leading a team, including supporting personal development. Prior experience delivering R&D projects within an industry (pharma / biopharma) environment would be highly advantageous. An agile mind-set, happy working within a fast-moving R&D environment with evolving priorities. The ability to deliver to deadlines and take a proactive approach to problem solving. Excellent communication skills, a collaborative approach and a personable nature to support relationship building within the broader team and key stakeholders. Please apply online or contact Katie-May Kress at CY Partners for more information. Key Words Senior Scientist, Scientist, Senior Research Scientist, Research Scientist, Laboratory Study Lead, Study Lead, Laboratory Project Lead, Project Lead, R&D, Research and Development, Pharmaceutical, Biopharmaceutical, Biologicals, Large Molecule, London, North London 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 Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

Head of Quality Location: Newcastle Monday Friday (35.5 hours/week) Salary: From £57,825 per annum (dependent on experience) + Excellent Benefits CY Partners looking for an experienced and forward-thinking Head of Quality to lead a Quality Control Department. This is a pivotal leadership role with responsibility for driving a shift in quality culture, moving from compliance-focused practices to capability-led processes with a Quality Technician as a direct report. Key Responsibilities: Lead and embed a capability-driven quality culture across operations. Develop and implement quality strategies focused on prevention and process improvement. Define, monitor, and report on key quality KPIs to track process capability, performance trends, and external performance. Partner with Operations, Process Engineering, and R&D to integrate quality into product design. Manage inspection plans in line with regulatory standards and product specifications. Champion best practice in Quality Improvement, coaching and developing internal teams. Ensure compliance with all quality standards and manage non-conformance processes. Support Operational Excellence initiatives across the business. Skills & Experience: Degree in Engineering or Chemistry. Lean Six Sigma Black Belt certified. Hands-on experience with SPC, FMEA, Six Sigma, and Lean tools. Proven track record in a manufacturing or engineering environment polymer experience is advantageous. If you re a quality-driven leader ready to make a real impact in manufacturing, we d love to hear from you apply now!

Microbiology Analyst Location: North London Permanent - Full Time - Mon-Fri Salary: £26,000 Do you have experience testing pharmaceutical samples using microbiology techniques? Are you looking for an exciting new role in the pharmaceutical industry? Our client, a leader in delivering high quality, processed biological materials is seeking an experienced Microbiology Analyst to join their dynamic team. If successful, you will be responsible for performing and validating a variety of microbiological tests, as well as reporting any deviations for investigation. Key responsibilities of the Microbiology Analyst include: Conducting microbiological testing and validation, including but not limited to: Bioburden Testing, Sterility Testing, and Microbial Identification. Following Standard Operating Procedures (SOPs) and GMP policies. Analysing results and conducting trend and statistical analysis. Reporting any deviations and assist with investigations. Maintaining calibration, functionality, and cleanliness of laboratory equipment. Prepare reagents, standards, and samples, ensuring good stock control. Participating in internal and external audits to ensure compliance with GMP, laboratory safety protocols, and record keeping practices. Maintaining accurate laboratory records organising assigned work activities, ensuring any delays are reported in a timely manner. To be considered as a Microbiology Analyst , you will need the following skills or experience: A BSc/MSc in Biochemistry, Microbiology, Biomedical Science, Biology, Pharmacology, or another relevant scientific discipline, or equivalent work experience. Previous experience working in a microbiology laboratory environment, ideally within the pharmaceutical industry. Strong understanding of microbiological principles and aseptic techniques. Experience performing routine microbiology techniques, including but not limited to: Sterility Testing, Endotoxin Testing, Bioburden Testing, Microbial Enumeration, Microscopy, and Microbial Identification. Excellent analytical and problem-solving skills to interpret data and troubleshoot issues within the laboratory. Strong communication and interpersonal skills to collaborate with colleagues and report scientific results. This is an excellent opportunity for a passionate Microbiologist to join an enthusiastic team and make a significant impact in a growing company. Please apply online or contact Katie-May Kress at CY Partners for more information. 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 Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

CY Partners Recruitment is delighted to be partnering with growing Biotechnology company based in Newcastle with their search for a Quality Assurance/Regulatory Affairs (QARA) Officer. Reporting to the QARA Manager in this key role you will ensure compliance with quality standards, regulatory requirements and best practice within the organisation. This is an exceptional role for someone who is looking to take a step into a dynamic environment, with projected significant growth for the organisation and the post-holder. Main Duties and Responsibilities - Document Control responsible for the document control system ensuring accurate and up to date records of procedures and quality related documents. - Corrective and Preventative Actions (CAPA) overseeing the CAPA process which involves identifying and addressing issues, deviations and non-conformities to improve product quality and compliance. - Change Management coordinating changes to processes, products or systems while maintaining quality standards. - Technical Files working with the quality team to create and update product technical files. - Develop, implement, and manage quality systems designed to ensure continuous production/service that meets established standards and customer specifications. - Perform routine inspections to verify compliance with company and regulatory requirements. - Analyse data to identify areas for improvement in the quality system including troubleshooting product or process failures. - Coordinate with operations and development teams to ensure quality standards are understood and integrated in all areas. - Facilitate corrective actions and improvement strategies for non-conformances and quality issues identified during internal and external audits - Lead training sessions for staff on quality assurance processes, tools and standards to foster a quality-centric culture within the organisation. - Support the internal audit process and preparation for notified body audits. - Follow company quality procedures and promote quality practises within the organisation. - Support update of QMS for IVDR - Be proactive and show initiative regarding time management, work prioritisation and committing to time-critical tasks - Work cross functionally with other teams and functions across the business - Involvement in risk management To be considered for the role of QA/RA Officer, you ll need the following qualifications, skills and experience: - Bachelor s degree or equivalent experience in a Life Science subject. - Experience in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry. - Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar. - Knowledge of NC/CAPA investigations. - Excellent attention to detail regarding existing and new documentation. - Experience or knowledge of IVD medical devices and Quality Systems. - Positive, team-focused approach to working and problem-solving. - Competent with Microsoft Word, Excel, PowerPoint and SharePoint. Location The role is to be primarily based at the site in the Newcastle upon Tyne. Application Instructions: Please apply online here - CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

Permanent Position Competitive Salary + Excellent Benefits Based in London Do you have experience in molecular biology techniques such as DNA / RNA extraction, PCR, qPCR, ddPCR, capillary / agarose gel electrophoresis or magnetic bead-based techniques? Would you like to work for a ground-breaking diagnostics company in London? My client is developing a revolutionary new NGS-based diagnostic platform in an easy-to-use, sample-to-answer, cartridge-based system designed to generate actionable results direct from clinical specimens in a matter of hours. Due to continued growth, they are looking to hire outstanding scientific talent, including a Senior Research Assistant - Molecular Biology, to join the existing multi-disciplinary NGS platform development team, filling key roles in the rapidly expanding program. This role would suit an experienced molecular biologist looking to work for a revolutionary company with a solid technology foundation. Key Responsibilities of the Senior Research Assistant - Molecular Biology : Support NGS technology development, including development of molecular biology and biochemistry modules and transfer to cartridge-based workflow. Design and execute laboratory experiments in a timely manner. Provide detailed descriptions of experiments and complete analysis of data, suggesting next steps. Identify technical issues as they occur and troubleshoot. Effective management of required documentation in accordance with company quality management system and ISO 13485 standards. Support the resolution of technical problems encountered during experiments. To be considered for the Senior Research Assistant - Molecular Biology , you'll need the following skills and experience; A BSc or MSc in a relevant life science discipline such as Molecular Biology, Biochemistry, Genetics, or have equivalent working experience Proficiency with Molecular Biology and/or Biochemistry techniques including DNA/RNA extraction, PCR, qPCR, ddPCR, capillary/agarose gel electrophoresis or magnetic bead-based techniques. Ability to design, troubleshoot, perform and analyse experiments to generate high quality experimental output and analysis. Knowledge of Next Generation Sequencing (NGS) workflows, primarily on sample prep and NGS library prep. Ability to design, perform, troubleshoot and analyse experiments The capability to deliver to deadlines and take a proactive approach to problem solving. This is a great opportunity to join a leading Biotechnology company in London, who offer great career development and an innovative working environment. Key Words "NGS, Next Generation Sequencing, Molecular Assay, Molecular Biology, PCR, Polymerase Chain Reaction, qPCR, rtPCR, Senior Research Assistant, Senior Research Associate, Research Assistant, Research Associate, Scientist, London" Please apply online or contact Katie-May Kress at CY Partners for more information. 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 Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

Permanent Position Competitive Salary + Excellent Benefits Based in London Are you an experienced molecular biologist with industry experience in techniques such as DNA / RNA extraction, PCR, qPCR, ddPCR, isothermal amplification, capillary / agarose gel electrophoresis or magnetic bead-based techniques? Would you like to work for a ground-breaking diagnostics company in London? My client is developing a revolutionary new NGS-based diagnostic platform in an easy-to-use, sample-to-answer, cartridge-based system designed to generate actionable results direct from clinical specimens in a matter of hours. Due to continued growth, they are looking to hire outstanding scientific talent, including a Scientist - Molecular Biology, to join the existing multi-disciplinary NGS platform development team, filling key roles in the rapidly expanding program. This role would suit an experienced industry based molecular biologist looking to work for a revolutionary company with a solid technology foundation. Key Responsibilities of the Scientist - Molecular Biology : Perform laboratory based NGS technology development, including development of molecular biology and biochemistry modules and transfer to cartridge-based workflow. Design and execute laboratory experiments in a timely manner, with minimal supervision. Analyse experimental results, providing detailed conclusions ahead of suggesting next steps. Identify technical issues and work collaboratively with other teams to troubleshoot and resolve these. Effective management of required documentation in accordance with company quality management system and ISO 13485 standards. Support technical and scientific advancements through researching novel methodologies and approaches e.g. literature reviews and attending conferences etc. To be considered for the Scientist - Molecular Biology , you'll need the following skills and experience; A BSc, MSc or PhD in a relevant life science discipline such as Molecular Biology, Biochemistry, Genetics, or equivalent working experience Proficiency with Molecular Biology and/or Biochemistry techniques including DNA / RNA extraction, PCR, qPCR, ddPCR, isothermal amplification, capillary/agarose gel electrophoresis or magnetic bead-based techniques. Previous demonstrable experience in designing, troubleshooting, performing and analysing experiments to generate high quality experimental output and analysis. Knowledge of Next Generation Sequencing (NGS) workflows, primarily on sample prep and NGS library prep is highly beneficial. The capability to deliver to deadlines and take a proactive approach to problem solving. Excellent communication skills and a personable nature to support relationship building and delivery of scientific information. This is a great opportunity to join a leading Biotechnology organisation in London, who offer great career development and an innovative working environment. Key Words "NGS, Next Generation Sequencing, Molecular Assay, Molecular Biology, PCR, Polymerase Chain Reaction, qPCR, rtPCR, isothermal amplification, Scientist, Associate Scientist, Senior Research Assistant, Senior Research Associate, London" Please apply online or contact Katie-May Kress at CY Partners for more information. 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 Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

Chemical Process Engineer Cheshire Full time & Permanent CY Partners is recruiting for a Process Engineer to join a specialist manufacturer of chemical products located in Cheshire. Supplying unique products to the Chemical and Pharmaceutical Industry, they are in the process of major upgrades & renovations to the plant, are seeking to hire a Process Engineer to manage ongoing plant modifications. This position will be well suited to an experienced Engineer who is eager to take ownership of varied projects and make meaningful & impactive changes. The role: As the Process Engineer, you will be responsible for ensuring the safe, & efficient processing of materials, alongside managing plant changes & installations. Key duties will include: Design & implement safe & efficient changes to Plant & equipment. Leading the management of change process Assist process safety studies and deliver process safety improvements. Support the process safety engineering expert for new product development projects. Lead HAZOP & LAZOP coordination. Requirements Relevant qualifications in Chemical / Process Engineering or similar relevant field. Previous process / Chemical engineering experience on a COMAH site. Good understanding of process safety and process hazard identification and risk control methods (LOPA, ALARP, HAZID, HAZOP) Working knowledge of electrical, mechanical, and hydraulic systems If you are interested in this position, please apply using the link below. Alternatively, call Nathan Fairhurst on / for more information.

Chemistry Lab Technician Location: Gateshead Salary: £18,500 - £23,000 DOE We are delighted to be supporting an expanding pharmaceutical organisation in Gateshead in their search for Chemistry Lab Technicians . Due to continued high demand for their services positions are available for enthusiastic and talented individuals who have a passion for Chemistry and progressing their career in the pharmaceutical sector. The purpose of the Chemistry Lab Technician is to assist the Chemists to carry out the synthesis of pharmaceutical products. Other responsibilities include : Assist with the cleaning of equipment and work areasEnsure a high standard of housekeeping is maintained at all times and cleaning records for areas and equipment are completed on timeCompliance to the quality systems ensuring procedures are followed at all times and new issues of procedures are signed off within the required time scaleDevelop a basic understanding of Quality AssuranceEnsure Training Records are updated as applicable and are always available for review during audits The ideal candidate for this role would be someone with a qualification in Chemistry or a similar field. They will have good communication and organisational skills and be able to work effectively within a team. Full training will be provided by the organisation but a background and a passion for Chemistry is required. If this sounds interesting to you why not apply now with a copy of your CV Tagged as: Chemistry, Lab Tech, Organic Chemistry, Organic Synthesis 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 Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.