Regulatory affairs jobs in RedditchCreate job alerts

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

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

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across g

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

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

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

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. Provide strategic i

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’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

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

Senior Regulatory Affairs Contractor / Consultant. Broad exposure to end to end LCM across Europe, ranging from artwork implementation through to regulatory strategy. Strong focus on process development, documentation, and regulatory compliance standards.

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 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

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

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

Regulatory Affairs within the pharmaceutical industry. G&L have multiple positions available for Regulatory Affairs Manager. Identify potential regulatory challenges early and implement strategies to keep projects on track.

This role assists in creating, developing, and implementing global regulatory affairs procedures and educating others on global regulatory expectations and requirements. Represent Regulatory Affairs on project teams by attending team meetings and providing the required plans, procedures and regulato

A global entertainment leader is seeking a Director for Litigation, Competition & Regulatory Affairs in the EMEA region. The role involves advising on litigation and regulatory matters, representing the company before authorities, and ensuring compliance with laws. Candidates should possess a Juris

A leading pharmaceutical organization is seeking a Regulatory Affairs Manager to support product development and lifecycle activities. The role involves leading EU regulatory submissions, contributing to clinical regulatory strategies, and ensuring compliance.

As Director, Litigation, Competition & Regulatory Affairs, EMEA, you will be the primary litigation, competition and regulatory counsel for the Sony Interactive Entertainment (SIE) business in the EMEA region, including Europe and the UK. Director - Litigation, Competition & Regulatory Affairs, EMEA

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

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 telecommunications company is seeking a Regulatory Affairs Lead in Greater London.

The role will lead the regulatory team, interfacing with regulatory agencies like the MHRA, EMA, FDA, preparing and submitting regulatory documents, and managing risk. Lead training and mentorship initiatives within the regulatory affairs team, fostering regulatory expertise and growth within the or

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.

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

Demonstrated practical experience in digital device regulatory affairs (e. Author and/or review compliant digital device documentation for Health Authority submissions, applying agreed digital device global regulatory strategies, current regulatory standards and guidelines. Experience leading regula

Manager Regulatory Affairs #J-18808-Ljbffr. Regulatory Affairs ManagerLondon, United Kingdom## Join UsAt Vodafone, we’re not just shaping the future of connectivity for our customers – we’re shaping the future for everyone who joins our team. Who you are*** Strong analytical capability: De

We are seeking a Senior Regulatory Affairs Specialist to join the Life Sciences Group (LSG) EMEA Regulatory Affairs team. Regulatory Affairs or Clinical Regulatory experience (IVD, medical device, or pharma). Senior Regulatory Affairs Specialist.

A leading international telecommunications firm in London is seeking a Regulatory Affairs Manager.

A leading fintech company is seeking a Head of Legal to provide practical legal guidance and support across corporate governance, commercial contracting, and regulatory compliance. This role requires a qualified solicitor with significant experience in financial services and expertise in technology

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

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. Responsible for the delivery of telco regulatory compliance advice to t

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

At least 3 years' experience in Regulatory Affairs, Clinical Regulatory, or a related discipline within the IVD, medical device, or pharmaceutical sectors. Senior Regulatory Affairs Specialist (IVDR / CDx Performance Studies). You will play a key role in shaping regulatory strategies, driving timely

A leading nutritional health company is seeking a Regulatory Affairs & Quality Control Executive to join their Technical & Quality Control Department. Key responsibilities include compiling regulatory dossiers and managing product development.

A leading nutritional healthcare company located in Greater London is seeking a Regulatory Affairs & Quality Control Executive. Responsibilities include following standard operating procedures, compiling regulatory dossiers, and managing New Product Development projects.

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.

Regulatory Affairs & Quality Control Executive. Quality Control and Regulatory Affairs experience preferred but not essential. Compiling Regulatory dossiers for worldwide submission and liaising with Export customers.

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

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

At least 6 years of relevant experience in a Financial Markets Front Office environment, preferably in a Market structure or Regulatory affairs role, or a hands-on, delivery-oriented Financial Markets Regulatory Legal role;. Delivering on the core regulatory expertise required of the role in accorda

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