Technical Coordinator

Technical Coordinator - Food Manufacturing Salary Negotiable DOE + 24 Days Holiday + Health Plan + Professional Development Support South Manchester Do you come from a Technical or Specifications background in the Food & Beverage sector and want to progress into a more varied role, providing you with a platform to take on new responsibilities and work cross-functionally with a wide range of customers and departments? This rapidly growing family-owned Food Manufacturing company has received multimillion-pound investments and won numerous awards in recent years as a result of their focus on building a great work environment and a positive company culture. They supply to a variety of high-profile retailers and foodservice clients and have achieved BRC AA+ rating. As a Technical Coordinator, you will lead on specifications, ensuring accurate customer specs & retailer portals meet requirements. You will support NPD through spec sign-off, artwork approval and label compliance, while handling technical queries. You will also support audits, traceability and the wider Food Safety and Quality system. The ideal candidate will have strong specifications & customer-facing experience in a Food or Beverage Manufacturing environment and will have a good understanding of food legislation, labelling/artwork and BRC standards. If you’re looking to progress in your career as a Technical specialist by joining a growing business that invests in its staff, this is the role for you. Key responsibilities: Generate and manage customer specifications and retailer portals, ensuring full legal and compliance accuracy Support NPD by completing spec sign-off, artwork approval and label compliance checks Respond to technical customer queries and support key accounts with accurate information Assist with audits, including traceability and mass balance, maintaining compliance standards Support the food safety and quality management system, including non-conformance investigations and continuous improvement Ideal candidates will have: Strong experience managing customer specifications and retailer portals within a food or beverage manufacturing environment Solid knowledge of food legislation, labelling requirements and BRC standards Ideally holding relevant qualifications such as HACCP/Food Safety Level 3, Internal Auditor Training or a Food Science degree Apply today by clicking the link or emailing your CV to stuart.goble@reed.com

Operations Manager Location: Staffordshire, fully site based Salary: £50k to £60k per annum with £6k car allowanceOther benefits: 5% pension contribution, 3% employee, 5% annual bonus based on company performance, 25 days holiday plus Bank Holidays and Christmas New Year closure, private healthcare The Role We are seeking a technically capable and detail driven Operations Manager for a specialist pharmaceutical organisation focused on quality-of-life therapies. This role is responsible for the oversight, integration, and continuous improvement of core operational systems, ensuring all business activities are delivered efficiently, securely, and in full compliance with ISO 9001:2015 standards. You will take ownership of operational governance, quality systems, and infrastructure, ensuring alignment across finance, IT, HR, and facilities. This is a hands-on role with significant autonomy, requiring a structured and systems led approach to managing a highly regulated environment. Key Responsibilities Operational Governance and Compliance Develop, implement, and maintain company policies, procedures, and operational frameworks Ensure ongoing compliance with legal, regulatory, and industry specific requirements Act as the central point of coordination with external advisors including legal, regulatory, and compliance specialists Quality Management Systems, ISO 9001 Maintain and continuously improve the Quality Management System in line with ISO 9001:2015 standards Lead internal and external audit processes, ensuring documentation, controls, and corrective actions are robust and traceable Drive continuous improvement initiatives Facilities and Site Operations Oversee day to day site operations, ensuring facilities meet health, safety, and regulatory standards Manage supplier relationships, contracts, and maintenance schedules to maintain operational continuity IT Infrastructure and Systems Management Own relationships with outsourced IT providers, ensuring service delivery, system performance, and security compliance Support implementation and optimisation of business systems including Microsoft 365 and associated platforms Lead IT and security initiatives such as Cyber Essentials, system upgrades, and infrastructure improvements Finance Systems and Controls Manage financial operations including accounts payable and receivable, payroll processing, and pension administration Oversee financial reporting processes and internal controls, working closely with external accountants to ensure compliance and accuracy HR Systems and People Operations Manage HR systems and employee data, ensuring accuracy, compliance, and reporting capability Oversee structured recruitment, onboarding, and training processes Support employee relations About You Comfortable working autonomously while managing cross functional systems and processes Strong attention to detail, particularly in compliance, documentation, and process control Commercially aware with a focus on efficiency, scalability, and risk mitigation Skills and Experience Experience within pharmaceutical or similarly regulated environments Background in operations, business, or office management with exposure to systems and compliance frameworks Understanding of IT infrastructure, service delivery models, and cyber security principles Experience working with ISO 9001 or equivalent quality management systems

Calibration Laboratory Technician (UV-VIS Spectroscopy) Annual Salary: £24,500 - £27,000 Location: Essex, IG6 Job Type: Full-time, Mon-Fri Join a leading scientific company as a Calibration Laboratory Technician specialising in spectroscopy, particularly UV-VIS, and analytical chemistry. This pivotal role involves the preparation and certification of Certified Reference Materials (CRMs), enhancing the accuracy and reliability of laboratory standards globally. You will work within ISO 17025 and ISO 17034 accredited frameworks under the guidance of the Calibration Laboratory Manager. Day-to-day of the role: Prepare and certify Certified Reference Materials (CRMs) to meet international standards. Utilise advanced UV-VIS spectroscopy techniques and analytical chemistry expertise in daily operations. Collaborate with the Calibration Laboratory Manager and team to meet departmental goals. Manage multiple tasks and prioritise effectively in a busy laboratory environment. Maintain accurate job cards and documentation, support audit activities, and keep rigorous records. Support team members and contribute to a collaborative, high-performing work culture. Required Skills & Qualifications: BSc in Chemistry, Analytical Science, or a related field, or equivalent professional qualification in laboratory sciences. Strong experience or knowledge in spectroscopy, particularly UV-VIS, and skilled in calibration measurements, with meticulous attention to detail. Ability to manage time effectively and adapt to shifting priorities. Team-oriented with a proactive and flexible approach. A willingness to learn and follow protocols to maintain a compliance culture. The position offers a competitive salary and benefits package, along with opportunities for professional development in a supportive team environment. To apply for the Calibration Laboratory Technician position, please submit your CV detailing your relevant experience and how you meet the qualifications outlined above.

Field Applications Scientist (South UK / London Region) 12-month FTC Are you looking for an exciting opportunity to work with a highly skilled technical team supporting customers across the UK? Are you passionate about delivering training in a laboratory environment? Do you enjoy learning and supporting advanced analytical platforms and technologies? Are you motivated by providing outstanding customer support and technical expertise? The Opportunity We are seeking an experienced Biomedical Scientist or Applications Specialist to join a Field Applications team as a Field Applications Scientist. This role sits within a dynamic field-based group responsible for delivering high-quality technical and applications support across centralised laboratory solutions, with a strong focus on biochemistry platforms. You will join a collaborative and experienced team supporting primarily the Greater London area, with occasional travel across the wider South region. The team plays a critical role in ensuring successful system implementation, delivering expert customer training, resolving complex technical issues, and building strong, lasting customer relationships. Key Responsibilities As a Field Applications Scientist, you will: Support the installation, configuration, and validation of analytical systems Deliver high-quality customer training tailored to laboratory users Provide expert troubleshooting and applications support Assist with software updates, system optimisation, and product maintenance Support sales activities through demonstrations, technical input, and tender responses Build strong relationships with laboratory stakeholders, ensuring a high standard of customer satisfaction About You To be successful in this role, you will: Have a strong understanding of the IVD/diagnostics industry Bring experience from a hospital laboratory or a diagnostics/applications support environment Demonstrate excellent troubleshooting and problem-solving skills Be confident delivering training and engaging with laboratory professionals Be highly self-motivated, with the ability to work independently and manage your own schedule Take pride in delivering exceptional customer service and exceeding expectations Maintain and continuously develop your technical expertise Why Apply? This is an excellent opportunity to join a forward-thinking organisation with a strong reputation for innovation and quality, where you can further develop your technical expertise while working closely with customers and cutting-edge laboratory technologies.

Field Applications Scientist (South UK / London Region) 12-month FTC Are you looking for an exciting opportunity to work with a highly skilled technical team supporting customers across the UK? Are you passionate about delivering training in a laboratory environment? Do you enjoy learning and supporting advanced analytical platforms and technologies? Are you motivated by providing outstanding customer support and technical expertise? The Opportunity We are seeking an experienced Biomedical Scientist or Applications Specialist to join a Field Applications team as a Field Applications Scientist. This role sits within a dynamic field-based group responsible for delivering high-quality technical and applications support across centralised laboratory solutions, with a strong focus on biochemistry platforms. You will join a collaborative and experienced team supporting primarily the Greater London area, with occasional travel across the wider South region. The team plays a critical role in ensuring successful system implementation, delivering expert customer training, resolving complex technical issues, and building strong, lasting customer relationships. Key Responsibilities As a Field Applications Scientist, you will: Support the installation, configuration, and validation of analytical systems Deliver high-quality customer training tailored to laboratory users Provide expert troubleshooting and applications support Assist with software updates, system optimisation, and product maintenance Support sales activities through demonstrations, technical input, and tender responses Build strong relationships with laboratory stakeholders, ensuring a high standard of customer satisfaction About You To be successful in this role, you will: Have a strong understanding of the IVD/diagnostics industry Bring experience from a hospital laboratory or a diagnostics/applications support environment Demonstrate excellent troubleshooting and problem-solving skills Be confident delivering training and engaging with laboratory professionals Be highly self-motivated, with the ability to work independently and manage your own schedule Take pride in delivering exceptional customer service and exceeding expectations Maintain and continuously develop your technical expertise Why Apply? This is an excellent opportunity to join a forward-thinking organisation with a strong reputation for innovation and quality, where you can further develop your technical expertise while working closely with customers and cutting-edge laboratory technologies.

Field Applications Scientist (South UK / London Region) 12-month FTC Are you looking for an exciting opportunity to work with a highly skilled technical team supporting customers across the UK? Are you passionate about delivering training in a laboratory environment? Do you enjoy learning and supporting advanced analytical platforms and technologies? Are you motivated by providing outstanding customer support and technical expertise? The Opportunity We are seeking an experienced Biomedical Scientist or Applications Specialist to join a Field Applications team as a Field Applications Scientist. This role sits within a dynamic field-based group responsible for delivering high-quality technical and applications support across centralised laboratory solutions, with a strong focus on biochemistry platforms. You will join a collaborative and experienced team supporting primarily the Greater London area, with occasional travel across the wider South region. The team plays a critical role in ensuring successful system implementation, delivering expert customer training, resolving complex technical issues, and building strong, lasting customer relationships. Key Responsibilities As a Field Applications Scientist, you will: Support the installation, configuration, and validation of analytical systems Deliver high-quality customer training tailored to laboratory users Provide expert troubleshooting and applications support Assist with software updates, system optimisation, and product maintenance Support sales activities through demonstrations, technical input, and tender responses Build strong relationships with laboratory stakeholders, ensuring a high standard of customer satisfaction About You To be successful in this role, you will: Have a strong understanding of the IVD/diagnostics industry Bring experience from a hospital laboratory or a diagnostics/applications support environment Demonstrate excellent troubleshooting and problem-solving skills Be confident delivering training and engaging with laboratory professionals Be highly self-motivated, with the ability to work independently and manage your own schedule Take pride in delivering exceptional customer service and exceeding expectations Maintain and continuously develop your technical expertise Why Apply? This is an excellent opportunity to join a forward-thinking organisation with a strong reputation for innovation and quality, where you can further develop your technical expertise while working closely with customers and cutting-edge laboratory technologies.

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.