Regulatory jobs in HerefordCreate job alerts

TEAM LEADER / HOUSE MANAGER Location:Bromyard, Herefordshire Salary:£30,500 - £43,000 Hours:Full-time (37.5 hours per week), including one weekend in four & participation in the on-call rota Holidays:33 days per year MAKE A DIFFERENCE LEAD WITH PURPOSE A dedicated leader with a passion for tra...

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...

Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of...

Senior Regulatory Affairs Associate. Regulatory team and help take a breakthrough neuromodulation device through PMA submission and into the market. Playing a key role in FDA Q-Subs and cross-functional regulatory strategy.

Ability to draft regulatory provisions related to commercial contracts; experience in corporate transactions or commercial contracts is advantageous. Advise on regulatory aspects of payment services for both bank and non-bank PSPs and e-money issuers. Minimum of 5 years PQE within a Financial Reg...

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...

Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of...

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...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Strong understanding of ICH and regulatory authority requirements. Senior Regulatory Medical Writer.

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...

Facilitate cross-functional and team awareness and understanding of regulatory issues as appropriate. Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs. Understand regulatory implications of product st...

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...

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...

Facilitate cross-functional and team awareness and understanding of regulatory issues as appropriate. Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs. Understand regulatory implications of product st...

Over years 5 years working on a range of Regulatory documents.

Lead regulatory interactions with authorities such as the FDA, EMA, and national agencies, while overseeing the preparation and submission of high-quality regulatory documents (e. Manage external regulatory service providers to align with business objectives and support the development and mainte...

Provide strategic guidance on regulatory pathways, risk assessment, and regulatory trends affecting metabolic disease treatments. A successful 'Global Regulatory Affairs Vice President - Clinical' should have: ~10+ years of regulatory affairs experience in biopharma, with a focus on metaboli

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

You’ll be responsible for fostering strong relationships with key regulatory bodies, primarily the FCA, and ensuring that Lockton stays ahead of the curve on compliance and regulatory changes. Social network you want to login/join with: Lockton is seeking an experienced Head of Compliance to lead...

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.

Develop and execute regulatory strategies for metabolic disease drug development, ensuring compliance with FDA, EMA, and global regulatory requirements. Oversee clinical regulatory affairs (RA), ensuring alignment between clinical development and regulatory expectations. Provide strategic guidanc...

To provide high-quality, concise, and accurate regulatory documentation that meets the expectations of both clients and regulatory authorities. Perform literature searches using publicly available or commercial databases to verify citations, locate references, and gather background context or reg...

Comprehensive benefits package including 401k and medical insurance Innovative and embracive company culture Extensive career growth opportunities If you are an experienced clinical Regulatory Affairs expert in the Life Sciences industry and are excited about the opportunity to make a significant...

Over years 5 years working on a range of Regulatory documents.

Build a suite of dynamic KRI and KPI metrics to track performance Build and maintain a continuous KYC / CDD programme utilising technology to support volumes ensuring efficiency Represent the Risk function at external events as appropriate At least 10 years experience of working in Fraud and Tran...

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...

Develop and execute regulatory strategies for metabolic disease drug development, ensuring compliance with FDA, EMA, and global regulatory requirements. A successful 'Global Regulatory Affairs Vice President - Clinical' should have: ~10+ years of regulatory affairs experience in biopharma, w

We are working with a leading international law firm to hire a Regulatory Lawyer to join their dynamic risk and compliance team in London. In this role you’ll provide expert guidance on a range of regulatory and professional risk matters, supporting senior leadership in maintaining the firm’s hi

The Successful Applicant A successful 'Global Regulatory Affairs Vice President - Clinical' should have: 10+ years of regulatory affairs experience in biopharma, with a focus on metabolic disease indications (diabetes, obesity, etc. Job Description Develop and execute regulatory strategies

The regulatory team are focused on both regulatory compliance and customer need to ensure products meet the highest standards of quality and commerciality. Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. An experienced regulat...

Oversee clinical regulatory affairs (RA), ensuring alignment between clinical development and regulatory expectations. Comprehensive benefits package including 401k and medical insurance Innovative and embracive company culture Extensive career growth opportunities If you are an experienced clini...

This well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established EU Regulatory Affairs team. As EU Senior Regulatory Affairs Manager, you will support the creation of strategy and execution plans and manage regulatory submissions (e. As EU Senior Regulato...

Remain current with regulatory/market conditions and apply this knowledge in pricing.

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. Assist in the preparation and submission of...

You’ll be responsible for fostering strong relationships with key regulatory bodies, primarily the FCA, and ensuring that Lockton stays ahead of the curve on compliance and regulatory changes. Social network you want to login/join with: Lockton is seeking an experienced Head of Compliance to lead...

Stay up to date on regulatory trends &. Strong command of UK/EU regulatory frameworks. Senior Compliance Consultant – Financial Crime & Regulatory Compliance (Payment Services & E-Money).

You’ll be responsible for fostering strong relationships with key regulatory bodies, primarily the FCA, and ensuring that Lockton stays ahead of the curve on compliance and regulatory changes. Social network you want to login/join with: Lockton is seeking an experienced Head of Compliance to lead...

They are strengthening the team by hiring a Regulatory EU Lead, to be based in their offices in West London, hybrid working set-up.

Check the business logs of coverholders and/or Binders/Lineslips to ensure that all risks are recorded and adhere to the Underwriting Strategy, Underwriting Standards, legal and regulatory requirements and sanctions restrictions; Conduct coverholder and/or Binder/Lineslip audits as required in or...

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. Prior regulatory writing experience in the pharmaceutical industry, medical communications agency or CRO. If you're lo...

Check the business logs of coverholders and/or Binders/Lineslips to ensure that all risks are recorded and adhere to the Underwriting Strategy, Underwriting Standards, legal and regulatory requirements and sanctions restrictions; Conduct coverholder and/or Binder/Lineslip audits as required in or...

This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of high-quality, accurate, and compliant documentation to support global ...

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.

Advise on regulatory aspects of payment services for both bank and non-bank PSPs and e-money issuers. Minimum of 5 years PQE within a Financial Regulatory team, with strong knowledge of payment services and experience working with e-money businesses. Ability to draft regulatory provisions related...

To support in this development we are seeking a satellite regulatory and licencing manager, who will focus on the management and meeting of our regulatory compliance obligations across the EU. Lead on the regulatory and licencing strategy for Europe, including ensuring that licences are applied f...

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...

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...