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Smiths Interconnect | Division of Smiths Group plc Reports to: Global Operations Director Location: Dundee, Scotland About Smiths Interconnect Smiths Interconnect is a global leader in high-reliability electronic components and solutions, serving mission-critical applications across demand...

We specialise in delivering high-quality clinical and regulatory documentation across a wide range of therapy areas, including:. The Role: Senior Regulatory Writer. Prior regulatory writing experience in the pharmaceutical industry, medical communications agency or CRO.

Demonstrated success in regulatory strategy development, multi-project leadership, and managing high-level regulatory authority interactions. Act as a subject matter expert on global regulatory requirements, including for ATMPs, ensuring company-wide compliance and integrating relevant regulatory...

Strong understanding of regulatory tools like IUCLID, REACH-IT, and CHESAR. You'll have a seat at the table when it comes to shaping strategy, guiding policy, and mentoring the next generation of regulatory professionals. If you're driven by both science and strategy, and ready to take your regul...

The Regulatory Department is one of the largest in the country and is recognised by clients and other lawyers as being one of the best.

May act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. Reviews documents within a therapeutic area with respect to consistency with the team/corporate established strategy and document history, ensuring a con...

To deliver specialist waste, permitting and environmental advice to improve and maintain environmental regulatory compliance, reduce carbon emissions through minimisation, re-use and recycling of waste and increase business efficiencies, for example by optimising energy through waste including CH...

As we expand our footprint , we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. Don't miss this chance to be a part of Freyr's expansion and make your mark in the world of regulatory services. Let's redefine regulator...

Lead Discord’s regulatory responses in the EU/UK and Australia, assessing risks/opportunities and drafting compelling, accurate submissions. Track record of successful engagements with regulatory bodies across. Experience crafting regulatory submissions and responding to agency requests.

Providing innovative drug development plans, data gap analyses and international regulatory strategies for complex products within the changing regulatory environment. Contributing to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Clinical...

Regulatory Strategy Development: Lead the development of regulatory strategies for CTAs in alignment with EU regulatory requirements. Experience setting the regulatory strategy and leading regulatory submissions and other activities for a medicinal product is strongly preferred. The Regional Regu...

Develop and deliver high-quality regulatory documents in line with guidelines. Prior regulatory writing experience in the pharmaceutical industry, medical communications agency or CRO. At Complete Regulatory, we offer.

The Regulatory Compliance Manager will play a crucial role ensuring the business operations are executed within ethical boundaries set by the government and industry regulations to identify and alleviate regulatory- associated risks. Ensures the organization adheres to regulatory requirements and...

If you're driven by both science and strategy, and ready to take your regulatory career to the next level, this could be the ideal next step. Do you have management experience, a consultancy background, and want to evolve in a leading Regulatory function?. This is a rare chance to shape regulator...

The Regulatory Analyst will: -Work with internal departments on the development and review of marketing materials and correspondence to ensure that compliance with State and Federal requirements are met. Responsible for entering, maintaining, and monitoring identified projects in Logic Manager an...

Top ranked in Chambers UK and Legal 500; our Regulatory team are recognised as one of the best in the UK with a broad spectrum of knowledge and expertise. In this role, you will independently manage a litigation caseload, supporting the Regulatory team in delivering high-quality services to profe...

A key part of the role involves producing clear regulatory guidance, and designing and delivering training on regulatory guidance produced. Working closely with our Water Quality Policy team and drawing on evidence from across Natural Resources Wales (NRW), you'll contribute to the development of...

Demonstrated and substantial experience in leading/managing the creation of IND/IMPD and NDA/MAA components, briefing documents, responses to regulatory authorities. Regulatory Medical Writing Lead. The individual provides leadership with respect to all program documents and may act as the depart...

As a Regulatory Affairs Specialist, you will be responsible for managing the Switzerland Person Responsible for Regulatory Compliance (PRRC) and UK Responsible Person (RP) activities within the company's diagnostics division, following established procedures and processes. Implementing and ensuri...

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. This position will benefit anyone looking to build on their experience in regulatory writing, while working within a hig...

If you are passionate about tackling intricate engineering challenges using cutting-edge technologies, including AI and ML, join us on an exciting transformation journey in regulatory reporting within the Payments sector, as we evolve into a global utility that fosters expansion and sustainment o...

Quality Assurance and Regulatory Affairs Consultant. Professional growth and development: You’ll have the opportunity to work on a diverse range of projects, from writing and editing regulatory documents to providing oversight for outsourced deliverables to our clients. Our services include devic...

The Senior Manager, Regulatory Affairs will be a strategic thinker, responsible for researching and assessing regulatory precedence and contributing to regulatory strategies for development of Compass Pathways investigational drug programs. Acts as a regulatory representative on assigned project ...

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 responses and o...

Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better. Business Development at RQM+ is res...

We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Regulatory responses to health authorities. You’ll play a key role in interpreting and communicating complex scientific data clearly and accurately for regulatory submissi...

The role requires extensive experience in UK, EU, and global compliance and regulatory agendas, including but not limited to:. Lead the end-to-end management of security and compliance projects, ensuring initiatives align with regulatory requirements, business objectives, and risk frameworks. Reg...

The role involves developing and improving NRW's agricultural regulatory activities, supporting the Lead Specialist Advisor, and collaborating with Policy and Operations teams to enhance regulatory capabilities. We seek a confident individual with experience or understanding of the agricultural i...

Regulatory knowledge: Familiarity with key regulatory frameworks, including DCUSA, Balancing and Settlements Code, MSAD, and LLF Methodology. We are looking for an experienced Regulatory Reporting Analyst to coordinate regulatory submissions in line with our statutory obligations, as well as main...

We're looking for a Wealth & Trading Regulatory Compliance Manager with expertise in EMIR and MiFID to lead the implementation of the regulatory framework around derivatives. Expertise in regulatory requirements relating to consumer protection. Compliance is a key team that ensures Revolut's prod...

You will be studying toward your Level 4 Regulatory Compliance Officer Apprenticeship. This role involves working with Babington to ensure regulatory adherence, conduct audits, and support risk management processes. Adapting to Regulatory Changes: Continuously monitor and adapt to changes in regu...

Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory approval process for our clients. Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regulat...

Senior Medical Writer - Sponsor Dedicated - Regulatory - United Kingdom, homebased. Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables. Adheres to established regulatory standards...

Providing innovative drug development plans, data gap analyses and international regulatory strategies for complex products within the changing regulatory environment. Direct experience preferred in providing strategic regulatory planning from early-stage development up to marketing authorisation...

Get notified about new Regulatory Specialist jobs in. Regulatory Reporting Implementation Specialist. Regulatory Affairs Specialist (Orthopaedic Reconstruction).

Responsible for regulatory clinical trial applications, annual reports, IND and IMPD amendments, and meeting requests to regulatory agencies. This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical throug...

Lead and support regulatory projects on behalf of the client including liaising and negotiation with regulatory authorities. We are looking to expand our Regulatory Affairs team and are currently looking for an experienced Regulatory Consultant to join us on a one-year fixed contract or a permane...

Senior Regulatory Affairs Associate – Contract – Pharmaceuticals. Active participation as regulatory affairs representative in meetings with internal & external stakeholders, working cross-functionally to achieve the business goal. As a product owner, providing comprehensive regulatory advice to

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. Act as a reviewer and signatory during review of labeling ensuring that content complies with regulatory requireme...

Prior regulatory writing experience in a medical communications company, CRO or Pharma. A solid understanding of drug development and regulatory documentation requirements. This is an opportunity to advance your career in regulatory writing within a highly specialised, supportive, and reputable t...

Experience in leadership of cross-functional regulatory projects and implementation of global regulatory strategies. Offer strategic mentorship on regulatory matters and align regulatory strategies with corporate objectives. Join Thermo Fisher Scientific as the Senior Manager of Regulatory Affair...

We have an exciting and unique opportunity for you to join us as a Regulatory Auditor! We are an ambitious company and have a lot more to do for the benefit of our customers.

Associate/Senior Associate - Regulatory. Associate/Senior Associate - Regulatory. We have handled many thousands of regulatory cases over the last 20 years, covering case investigation, preparation and presentation.

Due to the growth of a medical devices company based in Cambridge, there is a need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company’s Quality Assurance and Regulatory Affairs Manager. Regulatory Affairs and Quality Assurance Assistant – Medical De

Lead internal audits to assess adherence to regulatory requirements and corporate compliance standards. Excellent analytical skills to assess upcoming regulatory changes and their implications. Adaptability to evolving regulatory landscapes.

Senior Manager, Regulatory Medical Writing. Managing Consultant @ Cpl Life Sciences | Life Sciences Specialist /Regulatory Affairs & Quality. Senior Manager, Regulatory Medical Writing.

DAC Beachcroft is seeking a talented commercial and regulatory lawyer to join our highly successful, award-winning Commercial and Public Procurement team in London. This is an exciting opportunity to work closely with life sciences, medtech and digital health clients, as well as the team's wider ...

The Council as a landlord must demonstrate its compliance with the regulatory framework for social housing. This role focuses on an evidence based approach to that regulatory assurance along with data validation, performance analysis, with good practice research and application. Substantial under...

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. Typically requires at least 5 years of highly relevant experience in regulatory writin...

We're looking for a Wealth & Trading Regulatory Compliance Manager with expertise in EMIR and MiFID to lead the implementation of the regulatory framework around derivatives. Regulatory Compliance Manager (Wealth & Trading). Compliance is a key team that ensures Revolut’s products and processes m...

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. You will be a highly valued member of the Regulatory Writing team and will have the opportunity to advance your skills w...

You will report to the VP of Regulatory Affairs (US) and lead a team of European Regulatory Affairs personnel. Competent in dealing with regulatory authorities. European Head of Regulatory Affairs.

The National Speciality Lead for Regulatory and Expansion of Clinical Capability in Wales will contribute to the ATW Expert Clinical Forum, led by the Clinical Lead, to share sector intelligence and inform programme delivery against the Delivery Plan for Advanced Therapies in Wales. National Spec...

Regulatory Affairs Consultant - Cosmetics. Perform tasks associated with the Regulatory Affairs department at the highest level. Obelis Group is a quality driven, service-oriented company with over 30 years of experience in regulatory affairs.

Regulatory Compliance Officer Apprentice. Regulatory Compliance Officer Apprentice.

We have handled many thousands of regulatory cases over the last 20 years, covering case investigation, preparation and presentation. We act for a significant number of regulatory bodies, primarily in the health sector but, increasingly, more widely across a number of professional disciplines. Se...

Quality Assurance & Regulatory Affairs Specialist. An opportunity has become available for an experienced Quality Assurance and Regulatory Affairs Specialist to join the company on a permanent basis. This is a key role within the Quality and Regulatory team.

The successful candidate will provide regulatory support through monitoring programme assessments, policy reviews, and drafting essential documentation. Provide insightful regulatory advice and deliver consulting projects on financial crime topics such as AML, market abuse, and anti-bribery and c...

Engage with regulatory authorities and trade associations to anticipate headwinds and adapt to evolving regulatory standards. Act as the primary Regulatory interface for EU/UK, ensuring adherence to regulatory compliance and seamless collaboration across Quality, Supply Chain, NPD, and Sales. Sup...

Lead the development, writing, and editing of complex clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions (e. Stay current with industry trends, guidelines, and regulatory requirements. Regulatory writing experience th...

The ideal candidate will come with significant experience and interest in economic crime, with a criminal litigation background and good practical, working knowledge of the criminal justice system and regulatory landscape. Maintain an understanding of the latest developments in economic crime leg...

Regulatory responses and briefing documents. The Role: Senior Regulatory Writer. You’ll play a key role in writing and reviewing a broad range of regulatory documents, with a particular focus on strategic, high-level submissions for global health authorities.

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

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. Contribute to regulatory documents and reports for regulatory submission. Document and track regulatory s...

The Borough of Gravesham, situated in the northwest corner of Kent, covers 25,000 acres of varied countryside in southeast England.Bordered by the River Thames to the north, it is at the heart of the region's economic and cultural activities.

Are you a hands-on Regulatory Affairs professional with a passion for clinical trials and a drive to grow into leadership? Join a dynamic, fast-paced SME-sized CRO specialising in oncology, where your expertise will shape the future of our expanding Regulatory Affairs team. Regulatory Affairs wit...

Medicines and Healthcare products Regulatory Agency (MHRA). The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK’s sovereign regulator for medicines, including biological medicines, medical devices, and blood products.

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...

Artificial Intelligence [AI]) and ensure regulatory document templates, Medical Writing SOPs and Guidance Documents are produced and maintained to ensure consistency in format and best practice in accordance with appropriate regulatory requirements. Regulatory Medical Writing Manager. Regulatory ...

Work closely with the internal SLT team and ensure that updated are provided for the regulatory changes and trends. Good career progression opportunities with the potential of becoming the Regulatory Affairs Manager. I am working with a pharmaceutical/ Medical Device manufacturing site based in D...

Responsible for the implementation of the regional regulatory strategy, including the regulatory submission plans in line with agreed business objectives. The Regulatory Affairs Senior Manager provides regional (EU and other ex-US countries) support for all regulatory activities related to the on...

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 relevant regulatory metrics.

Act as the main point of contact with regulatory authorities and clients. Ensure regulatory compliance, quality, and on-time delivery. At least 10 years of experience in regulatory affairs and project management.

Support the development and implementation of regulatory strategies for both existing and new products, covering areas such as allergens, packaging, labelling, contaminants, and novel ingredients. Conduct detailed product compliance reviews for internal teams, including assessments of regulatory ...

Stays ahead of an evolving EOR regulatory landscape, anticipates, and identifies potential regulatory risks, advising leadership on proactive mitigation strategies and ensuring the business operates with a consistently risk-aware approach. Supports the Head of the department in the delivery of re...

May act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. Regulatory Affairs Specialist (Orthopaedic Reconstruction). Manager, EMEA Nuclear Regulatory Affairs.

In the Regulatory Affairs team, you’ll support and strengthen Monzo’s regulatory relationships and work closely with Executives to help shape our vision and regulatory affairs strategy as Monzo continues to grow. For Regulatory Affairs this means ensuring our regulators are kept informed, managi

In-depth knowledge of EU regulatory frameworks for biocidal products (BPR) and/or plant protection products (Regulation 1107/2009). Experience with global regulatory submissions (e. Are you an experienced Regulatory Specialist with experience working with Biocides and or PPP?.

Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget. Maintains familiarity with...

Engage with regulatory authorities and trade associations to stay ahead of regulatory changes. Support the Global Regulatory & Scientific Affairs (RSA) H&W Head in aligning business operations with regulatory requirements. Partner with corporate RSA teams to standardize and align regulatory proce...

Provides regulatory review and assessments for Home Care products to be marketed in the UK & Ireland. Drives the UK/I position on specific regulatory advocacy topics and related communication plan with other functions. PhD in Regulatory Toxicology (preferred), Chemistry, Toxicology, Biological Sc...

Generation and submission of high quality regulatory compliant documentation for all classes of product in Europe, USA and other global markets to ensure approvals are achieved in a timely manner. Maintain current registrations, licenses, Regulatory Certification, and submissions to ensure compli...

In this role you, will work with BioPharma partners on key projects, engaging with global regulatory agencies, and steering regulatory strategy for new product development and strategic initiatives. This position reports to the Director, Regulatory Affairsand is part of the Global Regulatory Affa...

As an Senior Manager, Global Regulatory Affairs, Precision Medicine, you will help develop and execute Precision Medicine regulatory strategy in alignment with the drug global regulatory strategy and in compliance with the appropriate IVD regulations. Provide Dx regulatory input to ensure complia...

Experience of understanding and applying regulatory activities. You will be expected to keep up to date with changing regulatory policy and proposed changes to legislation via membership of a relevant professional body or other equivalent means. Land Regulatory Approaches / Evidence, Policy and P...

The team consists of Regulatory Officers, Senior Technical Officers who lead and support our Regulatory Officers, and Digital Specialists who focus on delivering our digital requirements. Waste industry or regulatory experience is not necessary as you will receive full training. The Regulatory Of...

The Regulatory Department is very diverse, offering a broad range of expert advice to organisations and individuals facing Health & Safety, criminal, environmental, CQC and other regulatory prosecutions. The transport regulatory team is headed up by Chris Powell and sits within the wider Regulato...

An opportunity has become available for an experienced Quality Assurance and Regulatory Affairs Manager to join the company on a permanent basis. This is a key role within the Quality and Regulatory team, responsible for managing a small team across Production and Quality. Reporting to the Managi...

This is an exciting opportunity to join NRW's Land Regulatory Approaches team, in a Senior Advisor role. You will work with and support the teams' Lead Specialist Advisor, as well as other team members, Policy and Operations teams focussing on enabling and improving our agricultural regulatory ca...

Senior Regulatory and Start Up Specialist. Maintaining project plans, trackers, and regulatory intelligence tools. Regulatory or Start-Up specialist in CRO or pharma/biotech industry.

The Regulatory Compliance Manager works as part of a small team supporting the Senior Regulatory Compliance Manager to deliver regulatory compliance activities across E. Support the Senior Regulatory Compliance Manager with the drafting of formal and informal regulatory responses to consultations...

In collaboration with the medical and clinical operation team/ external regulatory consultants, assess adequacy of the non-clinical and clinical data package for regulatory submission based on available scientific guidance, precedence, previous experience and any scientific communication with any...

Our client's thriving Financial Services Regulation & FinTech practice is seeking an ambitious and energetic associate c.The firm has a market-leading technology practice and an impressive technology client base.Much of the work involves advising FinTech and other large technology and e-commerce ...

Experience in performing regulatory ecotoxicological risk assessments, ideally gained within industry, consultancy, or a regulatory agency. As a Regulatory Ecotoxicologist, you will join our established risk assessment team in delivering ecotoxicological risk assessments for plant protection prod...

Manage interactions with regulatory authorities, including the preparation of briefing documents and participation in regulatory meetings. Serve as the primary regulatory contact for sponsors, internal teams and regulatory agencies. Senior Regulatory Reporting Implementation Specialist.

Senior Regulatory Approaches Advisor, United Kingdom. Regulatory Approaches / Evidence, Policy and Permitting. This role offers the opportunity to join the Water Quality Regulatory Approaches team at Natural Resources Wales, focusing on water quality regulation across Wales.

Being innovative and demonstrating drive to achieve targets You will be expected to keep up to date with changing regulatory policy and proposed changes to legislation via membership of a relevant professional body or other equivalent means. Water Quality Regulatory Approaches Team/ Evidence, Pol...

Transform your regulatory expertise into innovative product success with this NPD & Regulatory Manager role at a leading natural beauty brand. This pivotal hybrid position combines strategic regulatory oversight with hands-on product innovation. Monitor regulatory changes and advise on potential ...

Lead and manage regulatory activities for biocidal or PPP products across the EU and/or global markets. Contracts - Experienced Regulatory Affairs Professionals - Manager to Director L. Regulatory Compliance Manager (Wealth & Trading).

Prudential Regulatory Reporting Accountant. Prepare Finance owned regulatory returns, including PRA and Bank of England returns, ensuring accurate, timely and consistent reporting to our regulators. Maintain, and develop where necessary, robust spreadsheets supporting the calculation of regulator...

This is an exciting opportunity to join a supportive in-house legal team, which provides support in the all the diverse aspects of local authority planning and regulatory law. You will be a qualified Lawyer, with experience in local authority related planning and regulatory enforcement.