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

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

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.

You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. This is a dedicated Regulatory Affairs Manager role supporting Colonis, a Clinigen Group company. To support our growth, we are seeking a dynamic, detail orientated and

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. Represent clients in interactions with regulatory agencies and provide solutions to regulatory challenges and objections.

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

Freyr's client is seeking a Regulatory Affairs Manager to fill a critical role in supporting development and execution of global regulatory strategies for investigational submissions, with a focus on EU and UK CTR. Provide critical support in developing global regulatory strategy, planning, and exec

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

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

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.

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

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

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 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

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

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

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

Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. In depth knowledge of UK and European regulatory affairs legislation and guidance. Ensure regulatory submissions are made on time and any delays

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

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.

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.

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

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

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. Document and track regulatory submissions and regulatory authority license approvals for the EU market, part

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

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

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

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

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

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.

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

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.

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

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

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

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

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.

Are you an experienced regulatory professional looking to shape global strategy and influence product development at an international level? This is an exciting opportunity to a global Pharmaceutical Manufacturing organisation as an Associate Director, Global Regulatory Strategy. Associate Director,

The successful candidate will have the freedom to shape regulatory strategy, influence business decisions, and represent the organization at regulatory and industry events. You will act as a key point of contact for global and regional regulatory authorities, lead submissions (CTA/MAA), and contribu

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

As the Senior Regulatory Affairs Manager, you will be accountable for providing regulatory leadership, strategy, and operational oversight for assigned marketed products and development projects. You will lead the UK & Ireland Regulatory Affairs team and act as the primary liaison with Health Author

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’ll support the quality and regulatory teams with keeping their processes and procedure in good shape. Ensuring processes related to quality/regulatory compliance are maintained. Updating policies, procedures and forms relating to QMS and regulatory compliance.