Trabajos regulatory en DundeeCrear alertas

Our client is a leading financial hardware provider with a global presence delivering payment solutions to consumers. As they continue to grow their offering, they are looking for a Lead Security Engineer with experience of Operational Technology assets to join the team working on a hybrid basis ...

Digital Architecture Manager Location: Scotland (Central Belt) Salary: From £64,680 plus benefits such as car allowance, pension and 38 days annual leave Our client, a major public sector, is undergoing a major digital transformation to improve how essential public services are delivered across S...

Electrical Commissioning Manager Newport Data Centres We are currently partnering with a leading Contractor who are active across the UK and Europe. Demonstrating success in an array of sectors including but not limited to, Data Centres, Pharmaceutical, Healthcare, Energy and many more. Due to ...

Residential Conveyancer Leading Newport Firm Are you an experienced Residential Conveyancer looking to take the next step in your career? Join a well-established and highly regarded law firm in Newport known for its friendly, professional, and client-focused approach. The Firm: Our client is a...

Its Guernsey office has an opening for an experienced lawyer to take on a role that spans a diverse range of corporate matters, but with a primary focus on investment funds and related regulatory issues. You will need a strong track record from a good commercial law firm and will have expertise i...

The Regulatory Labelling Lead role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases. Guiding the labeling team to develop and maintain Core Date sheets, USPI, SmPC and associated Patient Labeling doc...

You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expec...

This position involves the development of high-quality, accurate, and compliant documentation to support global regulatory submissions. You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variet...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Minimum of 5 years' regulatory writing experience in a medical communications agency or pharma/biotech setting. Strong understanding of...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to inte...

Business Development Manager – FCA/PRA Regulatory Compliance Consulting. You’ve spent 5+ years in BD roles within UK regulatory compliance, and you’ve outperformed. You’ve annually closed £250k+ deals in the regulatory space.

Understand regulatory implications of product strategy with regards to the product label & assessment. Ability to interpret and apply global and local regulatory guidance around labeling and associated supportive documentation. The Regulatory Labelling Lead role is part of a project with a leadin...

Healthcare Regulatory Solicitor/Associate/Senior Associate - Top Tier Firm – Hybrid/Remote working. Healthcare Regulatory team with additional Solicitors to join at various different levels. Qualified Solicitors in regulatory/health/social care/education law, join from Solicitor level up to Senio...

Business Development Manager – FCA/PRA Regulatory Compliance Consulting. You’ve spent 5+ years in BD roles within UK regulatory compliance, and you’ve outperformed. You’ve annually closed £250k+ deals in the regulatory space.

Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Assisting with the preparation and submission of regulatory documents to regulatory agencies. Supporting the RA Manager with Regulatory review of new product technical file documentation.

Senior Regulatory Advice Manager. In this pivotal role, you will be responsible for leading the Regulatory Advice team in providing clear, pragmatic, and timely advice to EUI both in terms of its day-to-day activities and for any change initiatives e. Support the design and implementation of an e...

Provide critical support in developing global regulatory strategy, planning and execution of global investigational submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). Research and apply regulatory intelligence and knowledge of strategic opt...

The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of the client’s products in the UK. We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our consulting co...

To provide high-quality, concise, and accurate regulatory documentation that meets the expectations of both clients and regulatory authorities. Author regulatory documents across various therapeutic areas, ensuring outputs are clear, factual, scientifically accurate, and free from over-interpreta...

As we expand our footprint to Warsaw, Poland, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navig...

General financial services law knowledge;Experience in handling regulatory and enforcement agency requests;. Experience with legal and regulatory requirements in relation to anti-money laundering/terrorist financing, the UK Bribery Act, and the Proceeds of Crime Act. Leading international law fir...

In support of the RA role, this position involves managing regulatory submissions, ensuring adherence to regulatory guidelines, cGMPs, ICH, and regulatory compliance, and collaborating with internal teams to support and facilitate drug development, and ensuring successful regulatory approval proc...

Proven experience as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents. Lead the development of ...

Senior Regulatory Counsel - United Kingdom. Reporting to the VP & Deputy General Counsel for Litigation and Regulatory Compliance, you’ll shape and lead our legal engagement strategy across the. Lead Discord’s regulatory responses in the EU/UK and Australia, assessing risks/opportunities and dra

Senior Regulatory Affairs Associate – Class III Devices | PMA Submissions | Remote + Monthly Onsite in Oxford | Equity + £100M Backed Start-up. Senior Regulatory Affairs Associate. Regulatory team and help take a breakthrough neuromodulation device through PMA submission and into the market.

Regulatory Reporting Analyst – 12 month contract. Prepare the Bank’s regulatory reporting with weekly, monthly and quarterly frequencies. Conduct robust data analysis to identify and inform trends in the relevant regulatory metrics.

Regulatory responses and briefing documents. At Complete Regulatory, we offer. We specialise in delivering high-quality clinical and regulatory documentation across a wide range of therapy areas, including:.

Sales Executive – Regulatory IT Solutions (Life Sciences). Ennov’s cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management.

Proven leadership in EU/UK submissions and regulatory agency engagement. Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using...

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

Excellent opportunity for a lawyer with experience in regulatory, environmental and/or health and safety to join a FTSE 100 business based in the West Midlands. You will have a high profile role within an established and experienced team advising on a variety of regulatory, civil and criminal inv...

We are looking to expand our Technical Regulatory team and are currently looking for a Vice President (VP) Technical - Clinical Development Regulatory Consulting to join us on a permanent basis. The Vice President - Regulatory Affairs (Technical) is a senior strategic expert responsible for suppo...

Compile product information for the preparation of technical files and regulatory dossiers to support product license applications and product licence maintenance for worldwide Regulatory Authorities. Manage, prepare and maintain regulatory documentation to enable the Company to comply with ISO13...

Regulatory Affairs navigates the complex regulatory landscape, ensuring the success of diverse clinical trials. Experience with the regulatory process in the UK and/or under EU-CTR (Poland, Denmark). As subject matter experts, the team leads submissions to regulatory authorities, coordinates with...

Our work spans a wide range of high-quality clinical and regulatory documents, including:. We’re looking for experienced Regulatory Writers who are both clever and curious, with a passion for science and precision. Write, edit, and review regulatory documents in accordance with guidelines and cli...

Develop robust regulatory strategies to ensure compliant and timely access to products compliant with the destination country's regulatory requirements. Provide regulatory support to sites requiring specific regulatory guidance to facilitate product supply. Serve as the primary Regulatory Affairs...

Regulatory Consultant – Electronic Medical Devices (IEC 60601 Focus). This role requires in-depth experience in regulatory affairs within active (electronic) medical devices. Their product is a connected therapeutic device set to transform remote care, but they need help navigating the regulatory...

Conduct global regulatory impact assessmentsfor product and manufacturing changes through the document control process; prepare and submit required regulatory updates. Act as the regulatory representative on cross-functional teams, collaborating with product development and manufacturing to integ...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

Experience in the Life Sciences, particularly in Regulatory Affairs and Regulatory Information Management. Principal Business Consultant - R&D - Regulatory (Remote). Principal Business Consultant - R&D - Regulatory (Remote).

This position involves the development of high-quality, accurate, and compliant documentation to support global regulatory submissions. You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variet...

Experience in preparing regulatory submissions and supporting regulatory strategy development. The successful candidate will contribute to Velsera’s regulatory strategy and regulatory submissions. The Regulatory Affairs Specialist will be an integral part of Velsera's Regulatory team, focusing on...

The Regulatory Labelling Lead role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases. Guiding the labeling team to develop and maintain Core Date sheets, USPI, SmPC and associated Patient Labeling doc...

The followingduties and responsibilities are crucial for a Regulatory Scientist specializing in digital endpoints to ensure successful regulatory approval and compliance:. Advanced knowledge of the regulatory science of digital endpoints, including regulatory procedures and strategies. Prepare an...

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

Experience in providing regulatory consulting advice to both established companies and new entrants either in-house, at a regulatory body or a consultancy;. Manager - Associate Director - Regulatory Advisory for Banking & Capital Markets. Banking & Capital Markets Regulatory Advisory.

Business Development Manager – FCA/PRA Regulatory Compliance Consulting. You’ve spent 5+ years in BD roles within UK regulatory compliance, and you’ve outperformed. You’ve annually closed £250k+ deals in the regulatory space.

We are looking for a dynamic and experienced Regulatory Reporting & Assurance Lead to join our team and support our clients in delivering high-quality, transparent, and robust regulatory reporting to stakeholders, regulators, and the public. As our Regulatory Reporting & Assurance Lead, you will ...