Regulatory affairs jobs in WisbechCreate 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. Represent clients in interactions with regulatory agencies and provide solutions to regulatory challenges and objections.

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

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

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

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

Senior Regulatory Affairs Contractor / Consultant. Strong focus on process development, documentation, and regulatory compliance standards. Experience supporting organisations expanding beyond the UK/EU, with awareness of broader regulatory considerations.

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

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

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

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

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. Review regulatory d

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

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

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

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. A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. They will wo

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

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. BSc / MSc Degree in

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. Responsible for the provision of full regulatory input and su

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

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

This is a one‑year secondment opportunity as the Head of Regulatory Affairs in the UK. Strong communication and coordination skills in order to achieve a consistent approach to engaging with the regulators in the UK and as necessary across the EMEA Division including the preparation and/or review

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

Candidates should have significant public affairs experience, a strong understanding of governmental processes, and excellent communication skills. A leading international energy and infrastructure business is seeking an experienced Head of Public Affairs for a 12-month fixed-term role in London. Th

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

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

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

Where appropriate, to act as the CMC Regulatory Lead on CMC Teams, representing the CMC Regulatory viewpoint and expertise on the CMC Team;* To identify potential CMC regulatory risks to the strategic / operational plans and propose options to mitigate risks;* To plan, prepare, review CMC component

Head of Spectrum & Regulatory Affairs. Head of Spectrum & Regulatory Affairs. Own the lifecycle of Open Cosmos’ spectrum assets, including the management and protection of ITU filings and regulatory rights.

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. Provide regulatory input on artworks and ensure approval in t

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. Maintaining positive and transparent relationships with the PRA and FCA

As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data while collaborating with a skilled global regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining

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

The position requires at least 5 years of drug development and regulatory experience. 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 t

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. Vast experience in the life sciences and/or pharmaceutical industry, focused to Reg

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

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 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.

At least 3 years' experience in Regulatory Affairs, Clinical Regulatory, or a related discipline within the IVD, medical device, or pharmaceutical sectors. You will play a key role in shaping regulatory strategies, driving timely submission packages, and ensuring the successful execution of complex

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

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

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. Regulatory Affairs and ot