Regulatory Submission Expert

As a Submission Operations Manager, you will play a key role in our Business Submissions & Operations (Regulatory Operations) team at UCB.About the role:Lead or participate as a Subject Matter Expert (SME) in the development of global processes and standards for regulatory submissions and technology projects.Ensure all dossiers comply with international and...

About the Role:ClinChoice is looking for a skilled Global Regulatory Submission Lead to oversee the development and implementation of regulatory strategies for EU clinical trials. This role involves leading regulatory activities, developing regulatory strategies, and managing interactions with regulatory authorities.Key Responsibilities:– Develop and...

About the RoleWe are seeking an experienced Regulatory Submission Manager to join our team in Brussels, Germany or Slough. As a key member of the Business Submissions & Operations (Regulatory Operations) team, you will be responsible for performing publishing and/or compilation activities for reports and submissions to Regulatory...

Blackfield Associates has a requirement for an Associate Director Regulatory Affairs to join their European HQ in Slough. This role involves leading regulatory submissions to EMA authorities and requiring a strong background in regulatory affairs.The ideal candidate will have at least 10 years of experience in regulatory affairs, preferably gained in a...

Are you a skilled regulatory professional looking for a new challenge? ClinChoice is seeking a Senior Regulatory Affairs Specialist to join our team in the UK. This is an exciting opportunity to work on global clinical trials and develop your expertise in regulatory submissions.In this role, you will be responsible for leading regulatory submission...

About the RoleWe are looking for a highly skilled Regulatory Affairs Principal Strategist to join our Clinical Operations team. As a key member of our team, you will be responsible for developing and implementing regulatory submission strategies for the European Union region. This role involves leading regulatory activities, developing regulatory strategies,...

Head of Regulatory ComplianceIn this critical role, you will oversee regulatory compliance and strategy for Blackfield Associates at our Slough-based European HQ.This is a permanent position requiring three days of in-office work per week. As a key member of our team, you must have a valid right to work in the UK and be unable to sponsor...

Regulatory Affairs DirectorWe are seeking a seasoned professional to lead our Regulatory Affairs team at Blackfield Associates' European HQ in Slough.This is a permanent role that requires hybrid working, with three days per week in the office. The successful candidate must hold a valid right to work in the UK and be unable to sponsor visas.Key...

Regulatory Affairs SpecialistWe are seeking a Lead Regulatory Specialist to join our team at Blackfield Associates in Slough. As a key member of our European HQ, you will be responsible for leading regulatory submissions and ensuring compliance with EMA regulations.This is a permanent role that requires hybrid working 3 days per week in our Slough office. To...

Senior Regulatory Strategy LeaderJoin us as a Senior Regulatory Strategy Leader at Blackfield Associates' Slough-based European HQ.This full-time role involves three days of in-office work per week. You must hold a valid right to work in the UK and be unable to sponsor visas.Key duties:Oversee submissions to regulatory agencies:PIC submissionsCTIS...

**Job Title**: Regulatory Lifecycle Specialist **Department**: RAQA **Reports To**: RAQA Manager **Position Summary**: Working under the guidance of the Quality Assurance and Regulatory Manager, the Regulatory Lifecycle Specialist will execute regulatory assurance activities, ensuring product life cycle compliance with identified regulations and standards...

**Job Summary:** We are seeking an experienced Regulatory Housing Expert to join our team on a temporary basis. The ideal candidate will have a strong background in housing regulation and be able to demonstrate a thorough understanding of the relevant legislation and guidelines.**Key Responsibilities:**Undertake HHSRS inspections of private sector...

About the role Are you an experienced Regulatory Affairs professional looking for a step up in your career? If the answer is ‘yes’ then perhaps this could be the career move you are looking for! We are working closely with a growing Pharmaceutical business with the hiring of a Senior Regulatory Affairs Manager – EMEA. Therapy areas...

At Blackfield Associates, we are seeking an experienced Associate Director Regulatory Affairs to join our team in Slough. This permanent role requires hybrid working, with a minimum of three days per week spent in the office.The successful candidate will have a strong background in regulatory affairs, with experience gained in the generics or R&D business....

Job OverviewWe are seeking a Senior Regulatory Affairs Manager to join our team at Blackfield Associates in Slough. As a key member of our European HQ, you will be responsible for leading regulatory submissions and ensuring compliance with EMA regulations.This is a permanent role that requires hybrid working 3 days per week in our Slough office. To be...

Our client, a global pharma company that's innovating in the Neurology and Injectables market, has a requirement for an Associate Director Regulatory Affairs to join their Slough based European HQ.To be considered for the role of Associate Director Regulatory Affairs, you will have experience in: 10 years plus regulatory experience, ideally gained in a...

Our client, a global pharma company that’s innovating in the Neurology and Injectables market, has a requirement for an Associate Director Regulatory Affairs to join their Slough based European HQ.To be considered for the role of Associate Director Regulatory Affairs, you will have experience in:10 years plus regulatory experience, ideally gained in a...

Our client, a global pharma company that’s innovating in the Neurology and Injectables market, has a requirement for an Associate Director Regulatory Affairs to join their Slough based European HQ.To be considered for the role of Associate Director Regulatory Affairs, you will have experience in:10 years plus regulatory experience, ideally gained in a...

Job Description:The Senior Regulatory Specialist position at Randstad Enterprise is a highly desirable opportunity for a professional to join our team on a 12-month contract. This role is part of our renowned global enterprise recognized for its widely acclaimed brands and products.Key Responsibilities:Evaluate and ensure compliance of ingredients, formulas,...

Job Overview">Randstad Enterprise, a leading provider of recruitment solutions, is offering a 12-month contract opportunity for a Senior Regulatory Specialist in Slough/Hybrid (1-2 days in the office). This role involves performing various regulatory activities related to raw materials, finished products, product registration, labelling, claims, packaging,...