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Regulatory Specialist I’m currently recruiting for a Regulatory Specialist to join an innovative and growing organisation within the animal nutrition sector. This role offers the opportunity to support regulatory activities for a global product portfolio while collaborating closely with technical and R&D teams. It would suit someone with a scientific background and early career experience in food or feed environments who is keen to develop their expertise in regulatory affairs. The Role As a Regulatory Specialist, you will help ensure products meet regulatory requirements across global markets while supporting both existing products and new product development. Working within a collaborative technical team, you will contribute to regulatory strategies, maintain product documentation, and assist with compliance across the product lifecycle. This is a hybrid role offering the opportunity to work closely with cross-functional teams including R&D, quality, production, procurement and supply chain. Key Responsibilities • Support regulatory activities for an established animal nutrition product portfolio, • Assist with preparation and submission of regulatory dossiers for product registrations and renewals, • Maintain product certifications and accreditations, including organic standards, • Prepare, review and manage technical documentation such as labels and data sheets, • Provide regulatory input during new product development activities, • Work with R&D teams on trials and regulatory requirements linked to product approval, • Respond to technical and regulatory queries from internal teams, • Contribute to internal reports and regulatory documentation as required Skills & Experience Essential • Bachelor’s degree in a scientific discipline (such as Animal Science, Biological Sciences or similar), • Around 1–2 years’ experience within a food, feed or nutrition environment, • Knowledge or interest in food safety or feed safety regulations, • Strong attention to detail and organisational skills, • Experience with regulatory processes in food or feed sectors, • Self-motivated with a proactive approach to problem solving, • Comfortable working within an international and multidisciplinary team, • Strong attention to detail and accuracy, • Flexible and adaptable, • A collaborative team player who communicates effectively with colleagues across functions Salary & Benefits • Salary: £36,000 – £40,000, • Bonus: Up to 10% performance bonus, • Pension: 7% employer contribution / minimum 1% employee contribution (with option to increase), • Life Assurance: 4x salary, • Health Cash Plan, • Holiday: 25 days annual leave + bank holidays (increasing to 28 days with long service), • Cycle to Work Scheme (after probation), • Employee Assistance Programme (EAP), • Location: Hybrid working Apply If you’re looking to develop your career in regulatory affairs within a collaborative and science-driven environment, this role offers a great opportunity to gain exposure to global regulatory processes and contribute to innovative animal nutrition products.

Regulatory Specialist I’m currently recruiting for a Regulatory Specialist to join an innovative and growing organisation within the animal nutrition sector. This role offers the opportunity to support regulatory activities for a global product portfolio while collaborating closely with technical and R&D teams. It would suit someone with a scientific background and early career experience in food or feed environments who is keen to develop their expertise in regulatory affairs. The Role As a Regulatory Specialist, you will help ensure products meet regulatory requirements across global markets while supporting both existing products and new product development. Working within a collaborative technical team, you will contribute to regulatory strategies, maintain product documentation, and assist with compliance across the product lifecycle. This is a hybrid role offering the opportunity to work closely with cross-functional teams including R&D, quality, production, procurement and supply chain. Key Responsibilities Support regulatory activities for an established animal nutrition product portfolio Assist with preparation and submission of regulatory dossiers for product registrations and renewals Maintain product certifications and accreditations, including organic standards Prepare, review and manage technical documentation such as labels and data sheets Provide regulatory input during new product development activities Work with R&D teams on trials and regulatory requirements linked to product approval Respond to technical and regulatory queries from internal teams Contribute to internal reports and regulatory documentation as required Skills & Experience Essential Bachelor’s degree in a scientific discipline (such as Animal Science, Biological Sciences or similar) Around 1–2 years’ experience within a food, feed or nutrition environment Knowledge or interest in food safety or feed safety regulations Strong attention to detail and organisational skills Confident communication skills and the ability to work collaboratively Desirable Experience with regulatory processes in food or feed sectors Knowledge of fermentation processes, silage inoculants or related microbiological manufacturing processes Personal Attributes Self-motivated with a proactive approach to problem solving Comfortable working within an international and multidisciplinary team Strong attention to detail and accuracy Flexible and adaptable A collaborative team player who communicates effectively with colleagues across functions Salary & Benefits Salary: £36,000 – £40,000 Bonus: Up to 10% performance bonus Pension: 7% employer contribution / minimum 1% employee contribution (with option to increase) Life Assurance: 4x salary Health Cash Plan Holiday: 25 days annual leave + bank holidays (increasing to 28 days with long service) Cycle to Work Scheme (after probation) Employee Assistance Programme (EAP) Location: Hybrid working Apply If you’re looking to develop your career in regulatory affairs within a collaborative and science-driven environment, this role offers a great opportunity to gain exposure to global regulatory processes and contribute to innovative animal nutrition products

You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. While the role is not primarily client-facing, you will engage directly with regulatory authorities, including participation in agency meetings The role requires someone

As a Principal or Senior Regulatory Affairs CMC Consultant, you will play a key leadership role, providing high-level regulatory and technical guidance for complex therapeutics. Principal / Senior Regulatory Affairs CMC Consultant. This role is with a rapidly growing international regulatory consult

Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for complex global requirements and regulatory challenges. Provide critical support in developing global regulatory strategy, planning, and execution of global investi

Associate Director – Regulatory Affairs CMC. CMC development and regulatory submissions. EU and/or US CMC regulatory requirements and ICH guidelines.

Title : Regulatory Affairs Associate - Regulatory Operations - Publishing. Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. Experience 2 to 5 years in Regulatory Affairs.

We're looking for an experienced Regulatory Affairs Manager to focus on financial crime related regulatory engagements, ensuring communication with external regulators is transparent, compliant, and efficient. The Regulatory Affairs team builds transparent relationships with regulators to keep Revol

The Regulatory Affairs Specialist reports into RA leadership and is responsible for regulatory compliance, regulatory submissions, and supporting regulatory planning and execution across the organisation. We are seeking a Regulatory Affairs Specialist with hands-on experience in software medical dev

It serves as the primary point of contact for regulatory and product safety matters, supports business decisions through impact assessments, and drives harmonization of stewardship processes, SDS, labeling, and regulatory proje. This role provides product stewardship and regulatory support for the C

Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experienced Risk Management Specialist to join its Quality & Regulatory team. Halianis currently recruitingfor an experienced Reg affairs Ri

For this reason, we’re looking for a Director of Regulatory Affairs to work closely with the existing regulatory team, internal and external experts, and contribute to the successful execution of our pivotal clinical program and commercialization. Maintain links with external regulatory network, p

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphas

Strong analytical strength for establishing effective and business relevant advice in the context of sometimes ambiguous legal, regulatory and political environments.

The Director, Regulatory Affairs leads a team responsible for developing and executing regulatory strategies for new and revised products in global markets. Minimum 15 years in medical device regulatory affairs and quality assurance. Lead, coach, and develop a high-performing NPI Regulatory Affairs

Provide ongoing regulatory support to the regulatory affairs team lead and project teams to ensure regulatory concerns are addressed and relevant data is generated to meet project objectives. Review tasks, support, and mentor Regulatory Affairs associates. Contribute to regulatory documents and repo

Maintain and organize regulatory documentation including job descriptions and resumes regulatory submissions correspondence with regulatory agencies and regulatory tracking databases. Collaborate with regulatory affairs teams to ensure alignment of training programs with current regulatory expectati

Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory affairs strategies for our Tether Data business vertical. Expertise in preparing complex regulatory documents and other major regulatory submissions, including the preparation and execut

Maintain and organize regulatory documentation including job descriptions and resumes regulatory submissions correspondence with regulatory agencies and regulatory tracking databases. Collaborate with regulatory affairs teams to ensure alignment of training programs with current regulatory expectati

You’ll be the go-to expert for regulatory and sustainability issues, driving advocacy and shaping the future of coatings.

A leading medical device firm in the United Kingdom is seeking a skilled Regulatory Affairs Manager. In this role, you will lead the Regulatory Affairs team and be responsible for managing registrations, certifications, and compliance. This position requires a strong background in medical device reg

A leading digital finance company is seeking an experienced Head of Regulatory Affairs to design and execute global regulatory strategies for their Tether Data business. Applicants should have a strong background in regulatory affairs and excellent communication skills. This role requires expertise

In depth knowledge of UK and European regulatory affairs legislation and guidance. Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. Solid understanding of pharmaceutical manufacturing processes

A prominent pharmaceutical company in the United Kingdom seeks a Regulatory Affairs Specialist to provide full regulatory support for products. The ideal candidate will have significant experience across the product lifecycle, particularly with CMC regulatory submissions.

An established industry player is seeking a Regulatory Affairs professional to join their dynamic team. In this role, you will contribute to regulatory documents and reports, manage submissions, and provide essential support to ensure compliance with EU regulations.

In depth knowledge of UK and European regulatory affairs legislation and guidance. Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. Solid understanding of pharmaceutical manufacturing processes

An established industry player is seeking a dedicated and experienced professional to lead a national approval team in the pharmaceutical sector.This role involves supervising team operations, ensuring compliance with quality standards, and fostering a collaborative environment.The ideal candidate w

A leading regulatory consulting firm in the United Kingdom seeks a motivated Senior Consultant. You will provide high-quality regulatory advice on human medicinal products, lead multi-country projects, and mentor team members. The position requires at least 5 years of drug development and regulatory

Graduation in pharmacy background or any relevant degree.Supervision and motivation of national approval team members.Contact person for all team members.Proactively ensuring smooth team operations and effective collaboration.Creating an inspiring team environment with an open communication culture.

The ideal candidate will have at least 8 years of experience in regulatory affairs within biotech and expertise in clinical trial applications and international regulatory dossier preparation. A leading biotech firm in the UK is seeking a Regulatory Affairs Director to transform the treatment of neu

This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands‑on experience with raw material data management. As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data wh

Lead multi-country projects and represent clients in regulatory interactions. Minimum 5 years of regulatory experience (FDA, EMA, MHRA or national authority). Experience authoring CMC sections of regulatory submissions; MAA/BLA experience preferred.

The ideal candidate should have a degree in a scientific field and substantial experience in regulatory affairs. A recruitment agency in pharmaceuticals is seeking a professional for a mid-senior level role focusing on regulatory input for product submissions. You will manage complex regulatory subm

Lead and inspire our Regulatory Affairs team, helping everyone thrive while managing registrations, certifications, and compliance. Experience in medical device regulatory affairs (MDD, MDR, IVDD, IVDR, UK MDR, ISO 13485). Are you passionate about regulatory affairs and want to play a key role in br

A leading regulatory solutions provider in the United Kingdom is seeking a Regulatory Affairs Manager to enhance quality management systems. The ideal candidate will have a Bachelor's degree, 2 years of experience in regulatory affairs, and knowledge of FDA and ISO standards. This position will ensu

An international medical device company based in the United Kingdom is seeking a Director of Regulatory Affairs. The ideal candidate will possess over 15 years of experience in regulatory affairs, preferably in the medical device sector, and have proven leadership abilities across multiple countries

A leading organization in regulatory affairs is seeking a Regulatory Affairs Manager based in the United Kingdom. Responsibilities include tracking employee training, maintaining regulatory documentation, and liaising with regulatory agencies.

A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. The successful candidate will leverage a minimum of 10 years of experience in Regulatory Affairs, involving detailed knowledge of large molecule biologics and FDA/EU regulations. This leaders

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Regulatory Affairs Manager (EU) | Leading Pharma. MAA, contributing to EU regional clinical regulatory st

Senior Regulatory Affairs Contractor / Consultant. Strong technical regulatory experience, particularly in Lifecycle Management (LCM). Broad exposure to end to end LCM across Europe, ranging from artwork implementation through to regulatory strategy.

You will oversee regulatory project management and act as a key partner to global Regulatory Affairs teams, R&D, Clinical Affairs, and wider cross‑functional groups. As Regulatory Affairs Manager, you will define and deliver UK/EU regulatory strategy across a diverse portfolio of products, includi

G&L have multiple positions available for Regulatory Affairs Manager. Regulatory Affairs within the pharmaceutical industry. Regulatory Information Management (RIM) systems.

Experience in Regulatory Affairs within the pharmaceutical industry. This role suits experienced regulatory professionals. Support regulatory capability and process development.