Regulatory affairs jobs in GraysCreate job alerts

Cancer Research UK is looking for an experienced regulatory affairs professional to join our Centre for Drug Development as a Regulatory Affairs Manager. Ability to apply specialist regulatory knowledge and experience to support the regulatory aspects of early phase drug development in the Charity.

The Regulatory Affairs Specialist role provides. Regulatory Affairs Department,. Notified Bodies and Regulatory Agencies.

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 Specialist (IVDR / CDx Performance Studies) Location: Warrington/UK-based (Remote or Hybrid) Contract: 12 months Hours: 37. You will play a key role in shaping regulatory strategies, driving timely submission packages, and ensuring the successful execution of complex reg

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

Monday-Friday (flexible) Start date: ASAP Salary: £60 per hour Are you an experienced Regulatory Affairs professional with deep expertise in IVD or Medical Device regulations across EMEA? This is an exciting opportunity to take a leading role in supporting regional regulatory strategies, en

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. We partner with leading pharmaceutical, biotechnology, and medic

You’ve built experience in a regulatory or quality-focused admin role, and you take pride in keeping things accurate, organised, and audit-ready. You’ll support the quality and regulatory teams with keeping their processes and procedure in good shape. Ensuring processes related to quality/regula

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

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

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

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

Associate Director – Regulatory Affairs CMC. CMC regulatory strategy across development and lifecycle programs. CMC regulatory documentation and CTD Module 3.

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

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

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.

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. Global Regulatory S

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

Halianis currently recruitingfor an experienced Reg affairs Risk Management specialist for a manufacturing client in theCotsworlds. Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experien

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

A major financial institution is seeking a Head of Regulatory Affairs for a 12-month fixed term contract. The ideal candidate will have strong knowledge of the PRA and FCA, excellent communication skills, and experience in regulatory affairs. The role involves leading regulatory engagement with UK r

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.

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

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

We are seeking an experienced Senior Regulatory Manager with strong expertise in EMA regulatory affairs to join their dynamic team. Strong regulatory affairs experience with a focus on EMA submissions. This role offers the opportunity to lead regulatory strategy, manage submissions, and act as a key

The Regional Regulatory Affairs Lead will provide sound regulatory advice, support the launch & re‑launch of products efficiently, ensuring all formulations and product claims meet legal requirements and align with company policies. Job Title: Regional Regulatory Affairs Lead. Manage a Regulatory

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 international energy and infrastructure business is seeking an experienced Head of Public Affairs for a 12-month fixed-term role in London. This position is integral to managing political and regulatory engagement vital for navigating the UK's complex energy transition. Candidates should h

We are looking for a Head of Regulatory Affairs (Director) to join our team! The role will help lead and maintain effective relationships with UK regulators. Strong communication and coordination skills in order to achieve a consistent approach to engaging with the regulators in the UK and as necess

A leading investment firm in London is seeking an individual to support its Public Affairs team in achieving regulatory objectives.

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

With an expanding product portfolio and a commitment to quality, safety, and regulatory excellence, the business is seeking an experienced Regulatory Manager to lead and strengthen regulatory operations. Regulatory Affairs Manager (Wound Care). As the Regulatory Manager, you will take ownership of a

A global staffing firm is seeking a Senior Regulatory Affairs Specialist for their EMEA team in Warrington. Candidates should hold a Bachelor's degree in Life Sciences and have over 3 years of experience in Regulatory Affairs.

Job Description:Job Title: Senior Manager, Regulatory Affairs CMCReports to: Executive Director, Regulatory Affairs CMCDepartment: Regulatory AffairsHours: Full timeLocation: UKAbout Autolus**Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial s

Head of Spectrum & Regulatory Affairs. Head of Spectrum & Regulatory Affairs. Act as the key regulatory interface for Mission Operations, Ground Segment and engineering teams.

We’re looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group. Coordinating responses to regulatory consultations and analysing publications from key regulatory bodies. Understanding of current regulatory priorities across the sectors in wh

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. Responsible for the provision of full regulatory input and su

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

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

As Head of Regulatory Affairs for the UK and Ireland, you will play a pivotal role on the Leadership Team, shaping and executing bold, forward-looking regulatory strategies across the entire pharmaceutical portfolio. Head of Regulatory Affairs – UK & Ireland. Advanced qualifications such as a PhD,

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

The Regulatory Affairs Lead provides expert telecoms and digital regulatory guidance across these lines of business, and acts as a key subject‑matter expert (SME) in implementing the Group Telecom Regulatory Compliance Policy. Accountable for Group Regulatory Compliance Policy Framework. Responsib

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

G&L have multiple positions available for Regulatory Affairs Manager. Regulatory Affairs within the pharmaceutical industry. Technical regulatory documentation.

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