Regulatory affairs jobs in RochdaleCreate 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

With expanding development programmes, evolving regulatory expectations and increased operational complexity, this is an exciting opportunity to step into a pivotal role that blends Regulatory Affairs and Quality Assurance. Minimum 5 years’ Regulatory Affairs experience, including IMP and clinical

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

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

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

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

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.

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

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

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. Title : Regulatory Affairs Associate - Regulatory Operations - Publishing. We partner with leading pharmaceutical, biotechnology, and medic

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

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

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

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

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

A growing medical device organisation near Watford is seeking a Regulatory Affairs Manager for Class I wound-care devices. Ideal candidates have over 5 years in regulatory affairs with expertise in UKCE marking and ISO 13485. The role entails leading regulatory compliance efforts, managing Technical

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

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

Arxada is seeking a Regulatory Affair Specialist accountable to the Senior Manager Regulatory Affairs for supporting the Professional Hygiene and Home Care regulatory programme. Regulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: UK - Manchester: PL - Warsawtim

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

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;. The key objective of the UK FM Regulation & Non-Financial Risk team is to m

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

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

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. Manage a Regulatory Affairs team supporting all brands in UK&I. J

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

Who you are*** Strong analytical capability: Demonstrated ability to develop clear, practical, and business relevant regulatory advice in complex and sometimes ambiguous legal, regulatory, and political environments. Manager Regulatory Affairs #J-18808-Ljbffr. Regulatory Affairs ManagerLondon, Unite

Author and/or review compliant digital device documentation for Health Authority submissions, applying agreed digital device global regulatory strategies, current regulatory standards and guidelines. Regulatory Affairs and other functional areas. Demonstrated practical experience in digital device r

Keep the heartbeat of innovation running and join our client in this Regulatory Affairs Labelling position and ensure cutting-edge pharma operations never miss a beat!. Proclinical is seeking a Regulatory Labelling Manager to support the development, optimization, and implementation of regulatory la

A global entertainment leader is seeking a Director for Litigation, Competition & Regulatory Affairs in the EMEA region. Candidates should possess a Juris Doctorate, excellent collaboration and communication skills, and substantial experience in regulatory environments. The role involves advising on

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. You will handle a wide range of litigation matters, working c

A global leader in innovative solutions is seeking a Regulatory Affairs Specialist to support their Professional Hygiene and Home Care regulatory programmes. The role involves leading regulatory strategy, ensuring products meet regulatory requirements, and providing expertise to the business.

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

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

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 bringing innovative medical devices to market? Join our growing, dynamic team where your work directly impacts patient safety and heal

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

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 financial services group is looking for a Head of Regulatory Affairs in Greater London. The role involves maintaining relationships with UK regulators, providing strategic advice, and ensuring compliance with regulatory requirements.

A governmental energy regulator in the UK seeks a confident leader to play a central role in protecting energy consumers and supporting the transition to a sustainable energy system.The successful candidate will lead multidisciplinary teams to deliver high-quality work in compliance, enforcement, an

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

The individual will lead projects, collaborate with cross-functional teams, and ensure compliance with regulatory standards.

A leading employment agency is looking for a Senior Regulatory Affairs Specialist to lead high-impact regulatory activities for IVDR Companion Diagnostics. This remote or hybrid role requires expertise in EU submissions and at least 3 years' experience in Regulatory Affairs. The successful candidate

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.