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What You’ll Be Doing: Manage compensation claims under the PFI agreement to maximise financial outcomes Draft, review, and negotiate contracts, ensuring legal and regulatory compliance Identify and manage commercial risks, minimising potential issues for the business Advise stakeholders on contra...

What Youll Be Doing Manage compensation claims under the PFI agreement to maximise financial outcomes Draft, review, and negotiate contracts, ensuring legal and regulatory compliance Identify and manage commercial risks, minimising potential issues for the business Advise stakeholders on contract...

Clinical Nurse Manager Deputy Manager When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order for your application to be reviewed. Position :Clinical Nurse Manager Care home :Springfield Vale Location :Barnsle...

About the Role As Manufacturing Engineer, you will play a critical role in supporting day-to-day production and driving continuous improvement across our manufacturing operations. Your focus will be on developing and refining processes that ensure product quality, operational efficiency, and on...

METTLER TOLEDO Safeline X-Ray provide premium product inspection technology to international customers who utilize our solutions to ensure public safety. We are committed to providing innovative and reliable solutions to our customers, and have a strong reputation for quality and expertise in ou...

Nursing Home Manager - Dementia Specialist Location: Barnsley Salary: £75,000 - £85,000 + up to £9k annual bonus Great Provider This is a fantastic opportunity to commission a brand new home with one of the best healthcare providers. This home will be a 30 bed dementia specialist home who are...

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. As a Regulatory leader, you will be responsible for leading the team and ensuring continuous imp...

Regulatory Finance Manager Salary £50,000 £74,000 per annum depending on experience Up to 10% bonus Permanent contract 40 hours per week Located in Leeds We have an amazing opportunity for a Regulatory Finance Manager to join our team based at Thorpe Park, Leeds on a permanent contract. What we

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.

Key Responsibilities: Serve as a member of the Regulatory and Quality Management Team for oversight and guidance of the entire organisation on RA and Quality strategy and activities Ensure that technical documentation and the EU declaration of conformity of the devices for which the business is t...

Previous experience producing regulatory documentation within a medical communications agency or pharmaceutical environment. Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety o...

Related duties include participation on design and risk management teams, initiation of regulatory plans for both new products and significant product modifications, documentation of regulatory impact from device modifications, assistance in creating and maintaining Technical Files, labeling/adve...

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. Independently produce hi...

What do we do? At Complete Regulatory, we provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory r...

Regulatory responses to health authorities. We’re looking for experienced Regulatory Writers who are both clever and curious, with a passion for science and precision. This is an opportunity to advance your career in regulatory writing within a highly specialised, supportive, and reputable team, ...

What do we do? At Complete Regulatory, we provide leading writing support and consultancy services to the pharmaceutical industry, producing high-quality clinical documentation such as clinical study reports, protocols, summaries, overviews, regulatory responses, and other supporting documents ac...

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...

What do we do? At Complete Regulatory, we provide top-tier writing support and consultancy services to the pharmaceutical industry, producing high-quality clinical documentation such as clinical study reports, protocols, summaries, overviews, regulatory responses, and other supporting documents a...

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...

Key Responsibilities Lead regulatory strategy and submissions across the UK, EU, and potentially the US Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment Advise internal stakeholders on regulatory risks and compliance Represent the company in external regulatory forums a...

Lead regulatory strategy and submissions across the UK, EU, and potentially the US. Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment. Advise internal stakeholders on regulatory risks and compliance.

Social network you want to login/join with: Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Liaise with regulat...

Reporting into our Head of Regulatory, Technical & Quality, you will spearhead the regulatory compliance team, managing the Regulatory & Technical compliance for all retail partners and the business's innovative range of cosmetic products. As a Regulatory Manager, you will join the Regulatory Com...

Key Responsibilities: Serve as a member of the Regulatory and Quality Management Team for oversight and guidance of the entire organisation on RA and Quality strategy and activities Ensure that technical documentation and the EU declaration of conformity of the devices for which the business is t...

Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. An experienced regulatory technologist with a minimum of 3 years in a cosmetic’s regulatory affairs. The regulatory team are focused on both regulatory compliance and customer ne...

What do we do? At Complete Regulatory, we provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory r...

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...

Coach and mentor more junior team members, providing support and guidance on client and project-related issues Be the point of contact for specific project deliverables, managing the technical and scientific aspects of leadership of designated client accounts/teams Take responsibility for the del...

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...

Coach and mentor more junior team members, providing support and guidance on client and project-related issues Be the point of contact for specific project deliverables, managing the technical and scientific aspects of leadership of designated client accounts/teams Take responsibility for the del...

Previous experience producing regulatory documentation within a medical communications agency or pharmaceutical environment. Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety o...

Social network you want to login/join with: Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Liaise with regulat...

Reporting to the Regulatory Affairs Manager, you will play a key role in supporting global regulatory submissions, maintaining compliance documentation, and ensuring adherence to regulatory standards for medical devices in the EU, US, and other markets. They're strengthening their Regulatory Affa...

We are looking to recruit Senior Regulatory Writers with at least 3 years' experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. We provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range...

Senior Compliance Consultant – Financial Crime & Regulatory Compliance (Payment Services & E-Money). Audits (financial crime, regulatory, safeguarding). AML, sanctions, fraud & regulatory compliance.

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.

Regulatory Technologist – Beauty & Personal Care. Are you a detail-driven Regulatory professional with a passion for the beauty industry? Do you love making sure amazing products stay compliant and safe while supporting NPD and innovation? If so, this could be your next career move!. Supporting t...

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...

The types of projects you might work on range from regulatory enforcements, environmental and. We are keen to hear from regulatory lawyers with experience gained in environmental and/or HSE issues. Excellent opportunity for a lawyer with experience in regulatory, environmental and/or health and s...

Guiding clients on regulatory strategy across the full product lifecycle. Regulatory experience with active or electronic medical devices. From digital health to complex electro-mechanical systems, we simplify regulatory complexity and enable innovation.

Satellite Regulatory Compliance Manager,. You will lead on the regulatory and licencing strategy for Europe, including ensuring that licenses are applied for and met in a timely manner. Strong understanding of EU regulatory frameworks and policy-making processes.

Assisting with the preparation and submission of regulatory documents to regulatory agencies. Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Ensuring compliance with regulatory requirements and guidelines (e.

Advising fee earners and business support teams on a wide variety of regulatory and compliance queries. Acting as a key contact on regulatory issues arising from new business intake, conflicts and AML queries. Monitoring legal and regulatory developments and contributing to strategic risk project...

Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical communications agency or pharmaceutical environment. Strong understanding of regulatory writing standards and processes ...

A minimum of 5+ years’ experience as a Regulatory Manager, Regulatory Team Leader, Regulatory & Compliance Manager, Regulatory Affairs Manager in the Cosmetics/Skincare/Haircare/Fragrance/Personal Care sector. If you are looking for a new role, get in touch today if you are an experienced Regulat...

Strong understanding of quality systems and regulatory frameworks - MUST HAVE IVDR regulatory expertise. If you are an experienced Regulatory Affairs candidate with IVDR regulatory expertise then please apply now!. As a Quality and Regulatory Specialist, you’ll play a key role in maintaining and ...

You'll be at the forefront of defining the approach for global governance, ensuring our regulatory and compliance needs are met holistically. EMEA regulatory framework, ensuring compliant launches of new products and services. Experience in rolling out regulatory change programmes.

Experience of Liquidity Regulatory reporting (e. Strong change management skills, ideally with regards to Regulatory implementation;. Working in the Liquidity and Product risk team, the role will support the change team that is responsible for implementing regulatory and business change required ...