Laboratory Analyst

Radiopharmacy Technician Annual Salary: £45,000 Location: Oxford Job Type: Full-time, Night Shift (12-hour rotating shift pattern, occasional Saturday shifts) Join a leading nuclear medicine company as a Radiopharmacy Technician. This role offers the opportunity to be involved in groundbreaking work in the production and quality control of PET radiotracers for clinical use. If you have a passion for science and innovation, and a commitment to excellence, this position could be perfect for you. Day-to-day of the role: Participate in the project phase, including drafting and executing validation protocols for the production and quality control of radiopharmaceutical products. Manufacture PET radiopharmaceuticals using advanced technology in a GMP environment. Perform aseptic dispensing and ensure sanitation of the production suites. Conduct quality control procedures to analyze the radionuclide and radiochemical purity of radiopharmaceuticals. Maintain rigorous standards of cleanliness and compliance in the facility, adhering to environmental, health, and safety guidelines. Pack and dispatch radiopharmaceuticals, ensuring compliance with local guidelines and transport regulations. Engage in continuous training and development activities, sharing knowledge and training staff as required. Required Skills & Qualifications: Science-related degree preferred. Experience in aseptic dispensing or radiopharmacy is desirable. Strong understanding of pharmaceutical chemistry and GMP. Familiarity with Ionising Radiation Local Rules, COSSH, and Health & Safety procedures. Excellent communication skills and the ability to work effectively as part of a team. High level of attention to detail and competence in managing multiple tasks simultaneously. Willingness to work flexible hours in a rotating 12-hour shift pattern. Benefits: Competitive salary, comprehensive training, and a dynamic work environment are part of the package. To apply for the Radiopharmacy Technician position, please submit your CV and a cover letter detailing your relevant experience and why you are interested in this role.

Senior Pharmacovigilance Scientist Location: Welwyn Garden City (Hybrid) Contract: 12-Month Fixed-Term Contract We are seeking an experienced Senior Pharmacovigilance Scientist to join a central safety operations team, focused on ensuring high-quality, compliant ICSR processing and safety data management to support patient safety. Key Responsibilities Oversee ICSR case processing and ensure compliance with global regulations Manage and monitor service providers, using metrics and performance insights Act as a subject matter expert, supporting stakeholders and regulatory inspections Drive process improvements and identify/implement CAPAs Assess the impact of new or updated regulatory requirements Experience Required Strong background in pharmacovigilance and ICSR processing Knowledge of global safety regulations (ICH, EU GVP, FDA) Experience in regulatory affairs and vendor oversight Proven ability to manage complex projects and influence stakeholders Desirable: medical device safety reporting experience Profile Proactive, quality-driven, and solutions-focused Strong communicator with the ability to simplify complex topics Adaptable, collaborative, and comfortable working in a fast-paced environment Please follow the link below to apply.

Senior Pharmacovigilance Scientist Location: Welwyn Garden City (Hybrid) Contract: 12-Month Fixed-Term Contract We are seeking an experienced Senior Pharmacovigilance Scientist to join a central safety operations team, focused on ensuring high-quality, compliant ICSR processing and safety data management to support patient safety. Key Responsibilities Oversee ICSR case processing and ensure compliance with global regulations Manage and monitor service providers, using metrics and performance insights Act as a subject matter expert, supporting stakeholders and regulatory inspections Drive process improvements and identify/implement CAPAs Assess the impact of new or updated regulatory requirements Experience Required Strong background in pharmacovigilance and ICSR processing Knowledge of global safety regulations (ICH, EU GVP, FDA) Experience in regulatory affairs and vendor oversight Proven ability to manage complex projects and influence stakeholders Desirable: medical device safety reporting experience Profile Proactive, quality-driven, and solutions-focused Strong communicator with the ability to simplify complex topics Adaptable, collaborative, and comfortable working in a fast-paced environment Please follow the link below to apply.

Senior Pharmacovigilance Scientist Location: Welwyn Garden City (Hybrid) Contract: 12-Month Fixed-Term Contract We are seeking an experienced Senior Pharmacovigilance Scientist to join a central safety operations team, focused on ensuring high-quality, compliant ICSR processing and safety data management to support patient safety. Key Responsibilities Oversee ICSR case processing and ensure compliance with global regulations Manage and monitor service providers, using metrics and performance insights Act as a subject matter expert, supporting stakeholders and regulatory inspections Drive process improvements and identify/implement CAPAs Assess the impact of new or updated regulatory requirements Experience Required Strong background in pharmacovigilance and ICSR processing Knowledge of global safety regulations (ICH, EU GVP, FDA) Experience in regulatory affairs and vendor oversight Proven ability to manage complex projects and influence stakeholders Desirable: medical device safety reporting experience Profile Proactive, quality-driven, and solutions-focused Strong communicator with the ability to simplify complex topics Adaptable, collaborative, and comfortable working in a fast-paced environment Please follow the link below to apply.

Temporary Laboratory Analyst Huntingdon, Cambridgeshire Temporary Contract (Full-Time) We are currently seeking a Temporary Laboratory Analyst to join a busy and dynamic laboratory team based in Huntingdon, Cambridgeshire. This is an excellent opportunity for someone looking to gain hands-on laboratory experience or build on existing analytical chemistry skills. Key Responsibilities: Carry out routine analytical testing in accordance with established procedures Prepare samples and reagents for analysis Operate and maintain laboratory instrumentation (e.g. HPLC, GC, or similar) Accurately record and report results in line with quality standards Follow laboratory health & safety and quality protocols at all times Assist with general laboratory housekeeping and stock management Candidate Requirements: Some analytical chemistry experience – either gained during a degree or within an industrial laboratory A relevant scientific qualification (e.g. Chemistry, Analytical Chemistry, or similar) preferred Strong attention to detail and good organisational skills Ability to work both independently and as part of a team Good communication skills and a proactive approach What’s on Offer: Valuable experience in a professional laboratory environment Supportive team and structured training Opportunity to develop practical analytical techniques This role would suit a recent graduate, laboratory assistant, or someone with entry-level analytical chemistry experience looking for their next opportunity.