Regulatory Affairs Consultant

6 days ago

London, Greater London, United Kingdom Clinical Professionals Limited Full time
Senior Regulatory Affairs Labelling Consultant

Job Type:
Permanent

Job Title:
Senior Regulatory Labelling Consultant (Labelling Strategy)

Location:
UK and Europe – Fully Remote

Salary:
Competitive Salary + Excellent Benefits

Employee Type:
Permanent

You will work as a regulatory affairs labelling lead for developing and establishing drug programs and be accountable for driving global labelling strategy.

This is a challenging opportunity to demonstrate your knowledge in managing regulatory processes and supporting cross-functional teams with labelling compliance.

This role can be based in the UK or Europe and offers the right candidate a chance to take the lead on regulatory labelling processes.

Conduct international labeling operations activities to support global new product and supplemental applications to product registration, and post approval launches for impacted international markets.


  • Collaborate with Technical Operations team members to ensure commercial distribution, Regulatory Technology for labeling submissions, PV for safety reporting, and other functional groups. Provide labeling to Advertising and Promotion for marketing pieces, and with Commercial for website postings if needed.
  • Work with Regulatory Operations, Regulatory Affairs, Tech Ops, etc. for labeling distribution, tracking and quality control.
  • Utilize regulatory/product knowledge to provide operational support to ensure that labeling materials meet regulatory and company requirements and timelines.

Be responsible for executing and effective quality control reviews and tracking (primarily) internally used labeling documents (Core Data Sheet, Core Patient Information Leaflet, Core Instructions for Use) and outward facing local/regional labeling (EU SmPC, EU PIL, etc) as well as container and carton labels to meet regional regulatory requirements and ensure consistency between labeling, labels and supportive documents.


  • Contribute to the continuous improvement of the end-to-end labeling process including excellent proofreading/editing skills and compiling supportive documentation.
  • Support labeling inspection / audit readiness activities
University Degree in a scientific degree
~4+ years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.
~ Regulatory Information Management System (RIMS), electronic document management system (EDMS). In addition, he/she should be capable of dealing with ambiguity, be creative, be comfortable working with multifunctional teams
~ Fluent in English written and spoken

  • Regulatory Affairs Consultant

    6 days ago

    London, Greater London, United Kingdom Michael Page (UK) Full time

    Our client is a fast growing medical devices consultancy, specialising in regulatory compliance, patents, clinical investigation and market entry. Ensure compliance with all relevant regulatory standards and guidelines within the healthcare industry. Develop and implement Regulatory Affairs and Quality Assurance strategies. Provide guidance and support to...

  • Ghs/clp Chemical Regulatory Affairs Specialist

    6 days ago

    London, Greater London, United Kingdom VRS Regulatory Full time

    An opportunity to join the Product Stewardship / Regulatory Compliance team at a global chemical business; you will ensure the compliance of globally sold, highly complex mixtures.Key duties will be SDS authoring, classifications, labelling, component compliance checks and providing regulatory advice to the technology, R&D, and customer service teams.This is...

  • Regulatory Affairs Consultant with| German

    6 days ago

    London, Greater London, United Kingdom Barrington James Full time

    Job Description Junior Consultant - QA/RA Position Overview: We are seeking a motivated Junior Consultant with 2-5 years of experience in Regulatory Affairs. This role requires hands-on involvement with the management of technical files, post-market regulatory activities, global device registration, and formulating regulatory strategies. Quality Assurance...

  • Regulatory Affairs Consultant

    6 days ago

    London, Greater London, United Kingdom Lifelancer Ltd Full time

    Regulatory Affairs Consultant Position at XYZ Pharmaceuticals Over 8 years of experience managing life cycle of approved drug products such as tablets, syrups, and injectables for EU market Deep understanding of regulatory framework and regional trends for various types of applications Leading and participating in the planning and delivery of regulatory...

  • Cmc Regulatory Affairs Consultant

    6 days ago

    London, Greater London, United Kingdom G&L Healthcare Full time

    We are an industry-leading independent scientific consultancy providing Pharmaceutical and Biotechnology clients throughout the world with expert Regulatory Affairs consultancy and Quality Assurance solutions.As demand for our services and solutions continues to grow we are looking for a CMC consultant to join our team of Regulatory Affairs professionals on...

  • Regulatory Affairs Consultant

    6 days ago

    London, Greater London, United Kingdom Barrington James Full time

    An exceptional opportunity awaits with our client, a dynamic Regulatory Affairs Consultancy with a presence in the UK, Switzerland, and Ireland, serving global clients. In this role, you will join a team of seasoned experts in Regulatory, CMC, Clinical, and Non-Clinical fields, leveraging your CMC and Regulatory expertise to provide comprehensive support and...

  • Regulatory Affairs Lead

    6 days ago

    London, Greater London, United Kingdom BioTalent Full time

    Regulatory Affairs Lead – Remote – Competitive PackageBioTalent are exclusively supporting an innovative UK based start up AI-backed software medical device company in their search for an experienced Software as a Medical Device (SaMD) Regulatory Affairs Lead. The company aims to effect large-scale population health improvement through the early...

  • Head of Regulatory Affairs

    1 week ago

    London, Greater London, United Kingdom Pop Science Full time

    We are delighted to be looking for a Regulatory Affairs Leader for our new client. Our client is dynamic and innovative clinical research organisation committed to providing expert consulting services to assist companies in accelerating the time to market of their investigational products. Specialising in optimising the drug development process, our team is...

  • Regulatory Affairs

    6 days ago

    London, Greater London, United Kingdom MSI Pharma Full time

    We are seeking an experienced professional to join our client's team as the Senior Director of Regulatory Affairs for the Northern European Cluster and Regional Skin & Essential Health Franchise. Based in the South-East of England you will work in a Hybrid work environment. In this role, you will be at the forefront of regulatory strategy, guiding product...

  • Regulatory Affairs Specialist

    6 days ago

    London, Greater London, United Kingdom Meet Recruitment Limited Full time

    Regulatory Affairs Specialist - Medical Device Job Title: Regulatory Affairs Specialist - Medical Device Fully remote We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team. As...

  • Regulatory Affairs

    6 days ago

    London, Greater London, United Kingdom i-Pharm Consulting Full time

    Regulatory Affairs Manager CMCDuration: 6 month Contract Inside IR35Location: Uxbridge, 3 days on-site per weekHourly Rate: £40-£55 per hour dependent on experience.This role focuses on the critical aspect of Chemistry, Manufacturing, and Controls (CMC) within regulatory affairs.Responsibilities include:Leading global regulatory strategies with a strong...

  • Regulatory Affairs Consultant

    6 days ago

    London, Greater London, United Kingdom Puraffinity Full time

    Rate: £500-£600 per dayDuration of contract: 3 months with ad hoc work thereafterLocation: London with regular office visitsAbout the companyPuraffinity Ltd is a rapidly growing start-up company. We are driven and strive to solve the global problem of toxic forever chemicals in water, working on several water treatment projects in parallel with an eye to...

  • Head of Regulatory Affairs

    6 days ago

    London, Greater London, United Kingdom The People Co. Assure Jobs Full time

    The Company and Role. A trusted partner within the food and consumer good market this progressive business work with a range of customer globally. The business currently seeks a highly skilled and experienced regulatory expert to play a key leadership role in navigating through the intricate regulatory requirements governing the food and drink industry. As...

  • Regulatory Affairs Specialist

    6 days ago

    London, Greater London, United Kingdom Meet Recruitment Limited Full time

    Regulatory Affairs Specialist - Medical Device 3 weeks ago Be among the first 25 applicants Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance...

  • Regulatory Affairs Specialist

    6 days ago

    London, Greater London, United Kingdom Hyper Recruitment Solutions Full time

    We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid...

  • Regulatory Affairs Executive

    6 days ago

    London, Greater London, United Kingdom Hyper Recruitment Solutions Full time

    Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely. As a Regulatory Affairs...

  • Regulatory Affairs Specialist

    6 days ago

    London, Greater London, United Kingdom Meet Full time

    Job Title:Regulatory Affairs Specialist - Medical DeviceLocation:Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.nOur commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overview:As a...

  • Senior Manager, Regulatory Affairs

    6 days ago

    London, Greater London, United Kingdom ICON Plc Full time

    United Kingdom- Remote or Hybrid (Reading, Swansea) At ICON, it's our people that set us apart. As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are...

  • Regulatory Affairs Strategist

    6 days ago

    London, Greater London, United Kingdom Parexel Full time

    Regulatory Affairs Strategist - UK/EU locations Parexel is seeking a Regulatory AffairsStrategist (Regulatory Affairs Consultant) with extensive experience in EU, US, and ROW markets. As a Regulatory Strategist, you will play a crucial role in providing regulatory representation in cross-functional teams, developing regulatory strategies, and advising on...

  • Regulatory Affairs Executive

    6 days ago

    London, Greater London, United Kingdom Takeda Pharmaceutical Full time

    People First - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. Our people are the heart of Takeda.Within our Regulatory Affairs department, we are looking for aRegulatory Affairs Executiveat our location...