Senior Regulatory Affairs Manager/ Consultant

1 month ago


England, United Kingdom Clinical Professionals Limited Full time

Senior Regulatory Affairs Manager/ Consultant
Job Type: Contract
Senior Regulatory Affairs Manager/ Consultant – 12 Months Contract 
Berkshire, UK – Hybrid
£60-70PH PAYE
We are partnered with a leading Pharmaceutical organisation who are looking for an experienced Regulatory Consultant to join on a 12-month contract basis. This product will support a combination product portfolio and will be driving European Regulatory Strategies and must be experienced in interacting with EU health authorities.
Define and implement Area & Affiliate regulatory strategies & deliverables for a portfolio of compounds typically marketed for the European area.
· Identify and advocate region’s requirements in the overarching global regulatory strategy; and make sure it is taken into account at the Global Regulatory Project Team (GRPT).
· Primary Regulatory Affairs (RA) interface with Commercial and in collaboration with the Regulatory Affairs personnel in the affiliates.
· Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external.
5 years of Regulatory experience with a strong background in EU submissions.



  • England, United Kingdom Mosaic Regulatory Solutions Full time

    Role- Senior Regulatory Affairs Specialist Location - Hampshire - Home working Some travel to site every few months for collaborative projects Supports Regulatory Affairs Project core team members on development teams, providing regulatory guidance, and project regulatory assessments. Liaises with internal functions such as Manufacturing, R&D,...


  • England, United Kingdom Mosaic Regulatory Solutions Full time

    Role- Senior Regulatory Affairs Specialist Location - Hampshire - Home working Some travel to site every few months for collaborative projects Scope: Supports Regulatory Affairs Project core team members on development teams, providing regulatory guidance, and project regulatory assessments. Liaises with internal functions such as Manufacturing, R&D,...


  • England, United Kingdom Clinical Professionals Limited Full time

    Regulatory Manager/ Senior Manager (UK) Job Type: Permanent Regulatory Affairs Manager/ Senior Manager – UK (line management) Berkshire, UK – Hybrid (3 days in the office) An exciting opportunity to join a growing pharmaceutical company and work as the UK lead and be responsible for the UK regulatory affairs team. This is a great opportunity to...


  • England, United Kingdom RBW Consulting Full time

    RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2...


  • England, United Kingdom RBW Consulting Full time

    RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2...


  • England, United Kingdom Clinical Professionals Limited Full time

    Regulatory Affairs Lead/Head of Department Job Type: Permanent Regulatory Affairs Lead/Head of Department An opportunity to work as a Regulatory Affairs Lead for a growing pharmaceutical company that specialise in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for an experienced leader who is personable,...


  • England, United Kingdom Hyper Recruitment Solutions Ltd Full time

    We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product information modifications. ...


  • England, United Kingdom Michael Page (UK) Full time

    About Our Client Our client is a globally recognised leader within the medical devices space. With a strong presence in over 100 countries, they are renowned for producing cutting-edge research and innovative solutions that have greatly impacted patients lives around the globe. Job Description Oversee and ensure all regulatory affairs are compliant...

  • Senior VP of Medical

    3 hours ago


    England, United Kingdom Beacon Therapeutics (USA) Inc Full time

    Are you a seasoned Senior Regulatory Leader looking for a new and exciting challenge? Beacon Therapeutics (USA) Inc is seeking a talented individual to join us as a Full Time Senior Vice President, Head of Global Regulatory Affairs, completely remote! In this role, you will have the opportunity to lead our global regulatory strategy and drive submissions for...


  • England, United Kingdom Michael Page (UK) Full time

    Our client is a globally recognised leader within the medical devices space. With a strong presence in over 100 countries, they are renowned for producing cutting-edge research and innovative solutions that have greatly impacted patients lives around the globe. Oversee and ensure all regulatory affairs are compliant with global standards. Develop and...


  • England, 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...


  • England, United Kingdom Hyper Recruitment Solutions Ltd Full time

    Head of Regulatory Affairs and Pharmacovigilance We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in...


  • England, United Kingdom Turner Lovell Full time

    UK Regulatory Manager (Offshore Electricity Transmission). Location: UK/ Remote Excellent salary package with bonus and benefits Sector: HVDC, Multi-Purpose Interconnectors, Offshore Renewables ~ Are you an ambitious and experienced Regulatory Manager, with a strong knowledge of HVDC and offshore transmission sector? Would you like to be at the...


  • England, 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...


  • South East England, United Kingdom WALKER COLE INTERNATIONAL LTD Full time

    Walker Cole International is currently supporting one of their Global Pharmaceutical clients in the South-East of England to hire a Regulatory Affairs Manager on a contract basis, outside IR35 or via umbrella company if needed. The key responsibilities are: - Provide a Regulatory strategy for submissions of new MAs and license maintenance variations - Work...


  • England, United Kingdom MSI Pharma Full time

    MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a UK based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the UK Responsibilites: Manage the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products...


  • England, United Kingdom RBW Consulting Full time

    RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2...


  • England, United Kingdom Hyper Recruitment Solutions LTD 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...


  • England, United Kingdom Hyper Recruitment Solutions Ltd 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...


  • England, United Kingdom SRG Full time

    SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic...