NPD Manager

Group Compliance Manager – Food Manufacturing 12 Months Maternity Cover £55,000 - £60,000 Wrexham Are you an experienced Technical or Compliance leader in the Food Manufacturing sector with demonstrable internal auditing experience and looking for a role with an incredible amount of responsibility for multi-site compliance? This leading Food Manufacturer specialises in ready meal solutions for big supermarkets & foodservice providers, having over 100 years of history and a strong footprint in the UK. They operate several modern production facilities and have benefited from significant investment in recent years. In this role you will be responsible for leading and delivering audit programmes across the company’s UK manufacturing sites, ensuring they consistently meet internal, customer and regulatory standards. You’ll play a critical role in identifying risks, implementing improvements and strengthening overall performance. The ideal candidate will have experience working as a Lead or Group auditor – or will have held this responsibility in a Technical or Compliance leadership role – where they have overseen multiple audit programmes and continuous improvement activities in line with BRC and major retailer standards. This is a fantastic opportunity for someone looking to step into a high-impact role at the group level where they will be able to significantly influence standards and performance across multiple sites. Day-to-day of the role: Leading and delivering internal audit programmes across multiple sites while ensuring technical teams are capable of carrying out their own internal audits Assessing site compliance against food safety, quality, and regulatory standards Identifying risks, gaps, and improvement opportunities, and supporting sites in implementing corrective actions Collaborating with technical and operational teams to drive audit readiness and best practice Monitoring trends and performance data to inform continuous improvement initiatives The ideal person will have: Significant experience in the Food Manufacturing sector as a Technical or Compliance leader, with a proven track record in carrying out internal audits Excellent knowledge of BRC standards and those of major retailers Demonstrable experience implementing or improving FSQA or Technical Management systems Full UK driving license and comfortable with travel to sites near London when required BRC Lead Auditor certification If you are interested in this position, click apply or contact Stuart Goble at Reed.

Product Development Manager Location: West Yorkshire Job Type: Permanent Salary: £50,000 - £55,000 p/annum plus benefits We are seeking a Product Development Manager to lead our client's product formulation and development function. This role is crucial for delivering innovation projects from concept to completion, managing the R&D Technicians team, and driving formulation excellence in alignment with our commercial objectives and regulatory standards. Day-to-day of the role: Lead the development, optimisation, and commercialisation of product formulations in accordance with the Innovation Programme and business strategy. Translate customer, market, and commercial requirements into innovative and commercially viable product solutions. Oversee formulation projects from concept through laboratory development, scale-up, validation, and production handover. Generate, analyse, and apply technical data to support robust product design, process development, and successful manufacturing scale-up. Identify opportunities for product enhancement, cost optimisation, and innovation. Maintain product formulations, Bills of Materials (BOMs), recipes, specifications, and associated technical documentation for product ranges. Manage multiple product development projects, ensuring delivery against timelines, budgets, and quality standards. Ensure all formulations and product developments comply with relevant regulatory, industry, and customer requirements. Lead, mentor, and develop the R&D Technicians and wider laboratory team, fostering a collaborative and high-performance culture. Required Skills & Qualifications: Degree or qualification in Chemistry or a related subject Proven experience in product development, formulation, or R&D management. Strong project management and organisational skills. Minimum of 3 years' experience leading or supervising technical teams. Excellent communication and cross-functional collaboration skills. Strong analytical and problem-solving abilities. Ability to manage multiple projects and deadlines effectively. Desirable: Experience with water-based dispersions To apply for the Product Development Manager position, please submit your CV detailing your relevant experience and why you are interested in this role.

Process Development Technologist – 1 Year FTC £35,000 Wrexham Are you an experienced Process Development or NPD professional in the Food Manufacturing sector with a passion for turning concepts into success solutions and looking for a high-impact role where you can work on projects for major retailers? This leading Food Manufacturer specialises in ready meal solutions for big supermarkets & foodservice providers, having over 100 years of history and a strong footprint in the UK. They operate several modern production facilities and have benefited from significant investment in recent years. This is a key role supporting the development and scale-up of new and existing food products, ensuring they can be delivered efficiently within a manufacturing environment. You will be working cross-functionally to bring concepts to life while balancing quality, cost and capabilities. The ideal candidate will have experience in the Food Manufacturing sector in an NPD or Process Development role where they have worked cross-functionally and developed a competence in Recipe, Nutrition & Yield Calculations. This is a great opportunity for someone early into their career to enhance their experience and bolster their CV by joining a big name in the Food Manufacturing sector on a 1 year contract developing products for high-profile clients. Day-to-day of the role: Supporting the development and sale-up of new and existing products to meet customer and business requirements Translating kitchen and concept recipes into viable factory processes Working with production, technical and commercial teams to ensure successful product launches Identifying and implementing process improvements to enhance efficiency, quality and cost-effectiveness Assisting with trials, documentation and validation The ideal person will have: 2+ years’ experience in NPD or Process Development in the Food Manufacturing sector An understanding of factory processes, scale-up and food safety standards Strong organisational skills with the ability to manage multiple projects at once Preferable holding experience with chilled products If you are interested in this position, click apply or contact Stuart Goble at Reed.

Quality Manager - Immediate Start Required 6 Month FTC, Permanent Position also Available Salary Negotiable + Vehicle or Vehicle Allowance + Perks Scunthorpe Do you come from an FMCG background where you have overseen BRC audits in a Quality or Technical Management role? Are you looking for your next contract opportunity where you can support a new Packaging site in securing BRC accreditation alongside a well-established business that has good processes & systems in place? This rapidly growing international manufacturer of sustainable packaging solutions operates a number of sites supplying products to the likes of the NHS, PlayStation, Tesco and Sainsburys. They are committed to reducing environmental impact through the use of recycled materials and innovative products, positioning themselves as a market leader that is built for the future. As a Quality Manager you will be responsible for preparing 2 of the company’s sites for upcoming announced BRC audits; one site is already AA rated and the other is gaining accreditation for the first time in line with a new product launch. You will be supported by a Quality Coordinator and an external Technical Consultant, and you will be working with already-established systems & procedures. The ideal candidate will come from a strong Quality, Compliance or Technical Management background in the FMCG sector where they have led and coordinated BRC audits. Experience within the Packaging sector is highly advantageous but not essential. If you’re looking for your next challenge - one where you can take full ownership of Quality & Compliance for a brand new manufacturing site that will be one-of-a-kind in the UK – this is the perfect role for you! Key responsibilities: Owning the site’s Quality Management System, making sure all documentation is kept up-to-date Ensuring 2 sites are ready for upcoming BRC audits - one in August, one in October Actioning and non-conformances, carrying out RCA and CAPA Making sure all staff are trained to sufficient levels on relevant procedures and FSQA practices The ideal candidate: Available to start in 0-2 weeks Demonstrable experience in a Quality, Compliance or Technical Management role in FMCG Previous responsibility for BRC audit readiness Apply today by clicking the link or emailing your CV to james.eaton@reed.com

Nonclinical Scientific Writer Welwyn Garden City 12-month temporary contract (outside IR35) Full time working hours We are working with a global healthcare organisation driven by a mission to deliver life-changing medical solutions today while advancing innovations for the future. They are seeking a Nonclinical Scientific Writer to join their Nonclinical Submission & Documentation Management team. This team collaborates closely with scientific and regulatory stakeholders to prepare high-quality, compliant nonclinical documentation and support successful regulatory submissions globally. Key Responsibilities Manage the preparation, review, and submission of nonclinical regulatory documents supporting early development and marketing applications Collaborate with regulatory and scientific teams to ensure accurate and comprehensive nonclinical dossiers for health authorities Partner with nonclinical project leaders and scientists to develop study reports, submission documents, and research-related materials Ensure documents meet internal standards and global regulatory guidelines (including ICH standards) Develop and maintain processes, tools, and best practices for high-quality document production About You Degree in a life sciences discipline Proven experience in scientific writing and editing within a nonclinical regulatory environment Strong proficiency with writing and document management tools, and an interest in adopting new technologies Excellent stakeholder management skills, with the ability to build trust across diverse teams Detail-oriented, with a strong commitment to producing high-quality documentation Proactive, accountable, and solution-focused in your approach to work If you are looking for new opportunities and possess the required skills and experience then please follow the link to apply.

Nonclinical Scientific Writer Welwyn Garden City 12-month temporary contract (outside IR35) Full time working hours We are working with a global healthcare organisation driven by a mission to deliver life-changing medical solutions today while advancing innovations for the future. They are seeking a Nonclinical Scientific Writer to join their Nonclinical Submission & Documentation Management team. This team collaborates closely with scientific and regulatory stakeholders to prepare high-quality, compliant nonclinical documentation and support successful regulatory submissions globally. Key Responsibilities Manage the preparation, review, and submission of nonclinical regulatory documents supporting early development and marketing applications Collaborate with regulatory and scientific teams to ensure accurate and comprehensive nonclinical dossiers for health authorities Partner with nonclinical project leaders and scientists to develop study reports, submission documents, and research-related materials Ensure documents meet internal standards and global regulatory guidelines (including ICH standards) Develop and maintain processes, tools, and best practices for high-quality document production About You Degree in a life sciences discipline Proven experience in scientific writing and editing within a nonclinical regulatory environment Strong proficiency with writing and document management tools, and an interest in adopting new technologies Excellent stakeholder management skills, with the ability to build trust across diverse teams Detail-oriented, with a strong commitment to producing high-quality documentation Proactive, accountable, and solution-focused in your approach to work If you are looking for new opportunities and possess the required skills and experience then please follow the link to apply.

Quality Assurance Assistant (Laboratory / Technical Environment) Aylesbury, Buckinghamshire Temporary – 6 months Full time working hours Role Overview We are looking for a detail-oriented Quality Assurance Assistant to support laboratory-based testing and customer projects within a fast-paced technical environment. This role will involve coordinating testing activities, maintaining high-quality documentation, and supporting the delivery of packaging and validation studies to meet customer and regulatory requirements. You will act as a key link between internal teams, external laboratories, and stakeholders, ensuring work is completed accurately, safely, and on time. Key Responsibilities Support the coordination and delivery of customer-driven technical projects in line with internal processes and timelines Create and maintain project documentation, including plans, reports, and test records Coordinate with internal teams and external laboratories to ensure testing activities are completed efficiently Review laboratory reports and support the preparation of final documentation in line with Good Documentation Practice (GDP) Maintain accurate records and ensure documentation is complete, consistent, and audit-ready Skills & Experience Required Previous experience in a QA, laboratory, or technical support role Experience within pharmaceutical, medical device, packaging, or cold chain environments Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint) Strong attention to detail, particularly in written documentation Ability to interpret technical specifications and quality requirements Familiarity with testing or quality standards (e.g. ISTA, ASTM, ISO) If you are looking for work, available to start within the next couple of weeks and possess the required skills and experience, then please follow the link to apply.

Quality Assurance Assistant (Laboratory / Technical Environment) Aylesbury, Buckinghamshire Temporary – 6 months Full time working hours Role Overview We are looking for a detail-oriented Quality Assurance Assistant to support laboratory-based testing and customer projects within a fast-paced technical environment. This role will involve coordinating testing activities, maintaining high-quality documentation, and supporting the delivery of packaging and validation studies to meet customer and regulatory requirements. You will act as a key link between internal teams, external laboratories, and stakeholders, ensuring work is completed accurately, safely, and on time. Key Responsibilities Support the coordination and delivery of customer-driven technical projects in line with internal processes and timelines Create and maintain project documentation, including plans, reports, and test records Coordinate with internal teams and external laboratories to ensure testing activities are completed efficiently Review laboratory reports and support the preparation of final documentation in line with Good Documentation Practice (GDP) Maintain accurate records and ensure documentation is complete, consistent, and audit-ready Skills & Experience Required Previous experience in a QA, laboratory, or technical support role Experience within pharmaceutical, medical device, packaging, or cold chain environments Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint) Strong attention to detail, particularly in written documentation Ability to interpret technical specifications and quality requirements Familiarity with testing or quality standards (e.g. ISTA, ASTM, ISO) If you are looking for work, available to start within the next couple of weeks and possess the required skills and experience, then please follow the link to apply.

Quality Assurance Assistant (Laboratory / Technical Environment) Aylesbury, Buckinghamshire Temporary – 6 months Full time working hours Role Overview We are looking for a detail-oriented Quality Assurance Assistant to support laboratory-based testing and customer projects within a fast-paced technical environment. This role will involve coordinating testing activities, maintaining high-quality documentation, and supporting the delivery of packaging and validation studies to meet customer and regulatory requirements. You will act as a key link between internal teams, external laboratories, and stakeholders, ensuring work is completed accurately, safely, and on time. Key Responsibilities Support the coordination and delivery of customer-driven technical projects in line with internal processes and timelines Create and maintain project documentation, including plans, reports, and test records Coordinate with internal teams and external laboratories to ensure testing activities are completed efficiently Review laboratory reports and support the preparation of final documentation in line with Good Documentation Practice (GDP) Maintain accurate records and ensure documentation is complete, consistent, and audit-ready Skills & Experience Required Previous experience in a QA, laboratory, or technical support role Experience within pharmaceutical, medical device, packaging, or cold chain environments Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint) Strong attention to detail, particularly in written documentation Ability to interpret technical specifications and quality requirements Familiarity with testing or quality standards (e.g. ISTA, ASTM, ISO) If you are looking for work, available to start within the next couple of weeks and possess the required skills and experience, then please follow the link to apply.

Process Development Scientist Location: Oxford Job Type: Full-time, Monday - Friday Join our innovative team as a Process Development Scientist, where you will play a crucial role in performing process development experiments to optimize manufacturing processes for solid dose delivery of vaccines and medicines. This position reports directly to the Head of Process Development and is pivotal in contributing to our mission of advancing healthcare solutions. Day-to-day of the role: Carry out laboratory-based experimentation to establish a robust, efficient, and scalable manufacturing process. Plan, execute, record, and report on scientific work accurately and efficiently. Perform analysis and interpretation of data, generating protocols, technical, and status reports. Support batch manufacturing activities in the laboratory for assigned internal and external projects. Coordinate activities with other team members both within and outside the immediate group. Proactively share experimental and scientific findings with colleagues. Work within a quality system to maintain traceable documentation. Adhere to company health and safety rules and promote safe practices. Required Skills & Qualifications: BSc/BEng degree in relevant material science, pharmaceutical engineering, or a related field. Minimum of 2 years’ lab-based experience in an R&D environment. Essential - Relevant experience in the formulation and process development of solid dosage forms. GMP experience is desirable. Experience in manufacturing processes such as powder blending and tableting is highly desirable. Benefits: 25 days holiday plus bank holidays 5% pension contribution Bonus scheme Company shares Private medical insurance Cash benefits Life assurance To apply for the Process Development Scientist position, please submit your CV and a cover letter detailing your relevant experience and why you are interested in this role.