CY Partners

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.

e-QMS Implementation Specialist A great opportunity has become available within an exciting medical devices organisation. The company is transferring paper records to an electronic QMS (eQMS) system. As an experienced Quality Assurance (QA) professional, you ll be knowledgeable of medical device regulations, and quality system implementation. The role focuses on migrating paper documents (SOPs, records, etc.) into a compliant electronic system while ensuring data integrity and adherence to ISO 13485 standards. Key responsibilities would include document review, data conversion, validation, and training, with a core requirement to maintain regulatory compliance throughout the transition. Working within a cross functional team, you ll project manage the implementation, including training to teams within the organisation. Key Responsibilities: Document Analysis and Migration: System Configuration: Work with the eQMS to establish appropriate document control and workflow templates, ensuring the system supports the company's quality processes. Validation and Quality Control: Implement validation procedures to confirm the correct migration and functionality of migrated documents and data within the eQMS. Regulatory Compliance: Ensure all migrated content and new processes comply with relevant regulatory standards, particularly ISO13485, for medical device quality management. Training and Support: Train personnel on how to use the eQMS for new document management processes and provide ongoing support. Audit Readiness: Prepare the eQMS for internal and external audits, demonstrating that all quality processes and records meet regulatory requirements. Required Skills and Qualifications: Regulatory Knowledge: Strong understanding of ISO 13485 and other relevant medical device regulations (e.g., FDA regulations). Technical Proficiency: Familiarity with eQMS software platforms and data entry tools. Document Control Expertise: Experience in managing and controlling documents, including their review, approval, and archiving. Problem-Solving Skills: Ability to identify and resolve issues that arise during the data migration and eQMS implementation process. This is an exciting role with labs based in Oxfordshire. The company has parcking on site and good public transport links. We look forward to receiving your application.

Microbiological Technologist Location: Barnard Castle Salary: £16.92 p/h (£33K per annum) Job Type: Full-time, 12 Month Contract Are you passionate about microbiology and looking to take the next step in your scientific career? CY Partners are excited to be supporting a global pharmaceutical company in their search for a Microbiological Technologist to join their dynamic team based in Barnard Castle . In this role, you'll play a key part in delivering high-quality microbiological testing and support across a variety of projects and routine operations. Working within a fast-paced GMP/GLP-regulated environment, you ll demonstrate your technical expertise across multiple microbiological disciplines while contributing to a culture of continuous improvement and scientific excellence. Key Responsibilities: Carry out a wide range of microbiological activities with a strong focus on Good Laboratory Practice (GLP) . Demonstrate multi-disciplinary skills and specialism in at least one core area of microbiology. Operate independently within your specialism, supporting site activities both at Barnard Castle and, if required, at other locations. Develop and validate new or modified techniques, including authoring of SOPs and Method Documents . Train and mentor other team members in specific technical procedures as directed by the Team Manager. Produce high-quality documentation, procedures, reports, and protocols within agreed timelines. Provide technical input and support for investigations and projects across the microbiology team. Analyse data and prepare reports for internal stakeholders and regulatory bodies. Participate in routine and non-routine environmental and product monitoring activities. About You: To be successful in this role, you ll need to bring a mix of practical lab experience, and a proactive attitude. We re looking for someone who is: Experienced in microbiological techniques. Confident working independently and taking initiative in solving problems. Strong communicator, both written and verbal, with excellent attention to detail. Comfortable managing priorities in a dynamic, collaborative setting. Why Apply? This is a fantastic opportunity to join a forward-thinking, science-led team within a global organisation that offers excellent career development opportunities. Whether you're looking to build on your current lab skills or grow into a more specialist role, this position offers the support and structure to help you thrive. CY Partners is acting as an employment agency/business in relation to this vacancy.

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.