Emplois actuels liés à Head of Global Labelling – Regulatory Affairs - Paris, Île-de-France - Cpl
-
Head of Regulatory Affairs
il y a 2 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinJob Title: Head of Regulatory AffairsJob Summary:We are seeking a highly experienced Head of Regulatory Affairs to join our team at Cpl Healthcare. As a key member of our regulatory affairs team, you will be responsible for providing expert regulatory knowledge and strategy to the business regarding healthcare industry regulatory requirements.Key...
-
Head of Global Labeling Strategy
il y a 4 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinJob Title: Head of Global LabelingJob Type: Full-time permanent positionLocations: UK, France, Germany, Ireland, Netherlands, Norway, and the United States of America (Remote)Remuneration: Competitive salary and benefits packageAbout the RoleWe are seeking a highly experienced and skilled Head of Global Labeling to join our team at Cpl Healthcare. As a key...
-
Head of Global Labelling Strategy
il y a 2 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinJob Title: Head of Global LabellingJob Type: Full-time permanent positionLocations: UK, France, Germany, Ireland, Netherlands, Norway, and the United States of America (Remote)Remuneration: Competitive salary and benefits packageAs a key member of the Cpl Healthcare team, you will play a critical role in shaping the company's global labelling strategy. This...
-
Global Labelling Strategist
il y a 2 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinJob Description:We are looking for a Global Labelling Strategist to join our team at Cpl Healthcare. As a key member of our regulatory affairs team, you will be responsible for developing and implementing global labelling processes for our pharmaceutical products.Key Responsibilities:Develop, implement and operate global labelling processes for a...
-
Regulatory Affairs Director
il y a 2 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinCpl Healthcare is seeking a highly experienced Regulatory Affairs professional to join our team as a Head of Compliance. This is a fantastic opportunity to provide expert regulatory knowledge and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations, and post-market compliance....
-
Head of Regulatory Affairs
il y a 2 semaines
Paris, Île-de-France Selby Jennings Temps pleinWe are seeking a Head of Regulatory Affairs to join our team in Paris. The successful candidate will be responsible for ensuring that our company adheres to all regulatory requirements, while promoting a culture of compliance across the business.Key Responsibilities:Maintain strong relationships with regulatory authorities and professional...
-
Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France Groupe ProductLife Temps plein{"h1": "Regulatory Affairs Specialist", "p": "At Groupe ProductLife, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for managing artwork generation, labeling, and creation/update of product information. This includes reviewing packaging texts, providing format...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinRegulatory Affairs SpecialistJoin Groupe ProductLife, a global industry leader in regulatory outsourcing and consulting services for the life sciences industry. We are seeking a highly skilled Regulatory Affairs Specialist to support our clients in managing artwork generation, labelling, and product information creation.Key Responsibilities:Manage the...
-
Associate Regulatory Affairs Professional
il y a 2 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob DescriptionWe are seeking a highly skilled Associate Regulatory Affairs Professional to join our Regulatory Affairs team. The successful candidate will be responsible for supporting the Head of Regulatory Affairs and assisting/working with the members of the Regulatory Affairs team in the execution of the strategic agenda with regard to regulatory...
-
Global Regulatory Affairs Lead
il y a 4 semaines
Paris, Île-de-France Sobi group Temps pleinJob Title: Global Regulatory Affairs LeadWe are seeking a highly skilled Global Regulatory Affairs Lead to join our team at Sobi. As a key member of our organization, you will be responsible for providing global regulatory leadership and strategic direction to ensure compliance with regulatory requirements and to drive business growth.Key...
-
Regulatory Affairs Associate
il y a 3 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob DescriptionRole SummaryWe are seeking a highly skilled Regulatory Affairs Associate to join our Regulatory Watchtower team in Paris. As a key member of our Regulatory Affairs department, you will play a crucial role in supporting our various departments in navigating banking supervision and related regulations.Main ResponsibilitiesMonitor regulatory...
-
Global Head of Regulatory Compliance
il y a 2 semaines
Paris, Île-de-France Worldline Temps pleinJob Title: Global Head of RegulatoryAt Worldline, we're shaping the future of payments technology. As our Global Head of Regulatory, you'll play a critical role in helping us navigate the complex landscape of governance and compliance.Key Responsibilities:Prepare and submit regulatory returns related to governance, ensuring accuracy and timeliness.Collect...
-
Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinAbout the JobWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Groupe ProductLife. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our clients in the pharmaceutical industry.Your primary focus will be on providing guidance and...
-
Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinJob SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Groupe ProductLife. The successful candidate will be responsible for coordinating and managing the Linguistic Review process for Centralized Procedure medicinal products.Key ResponsibilitiesCoordinate and manage the Labelling team in charge of the Linguistic Review...
-
Regulatory Affairs Associate
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob Title: Associate Regulatory AffairsWe are seeking a highly skilled Associate Regulatory Affairs professional to join our team at SGS Société Générale de Surveillance SA. As a key member of our Regulatory Affairs team, you will play a critical role in supporting our business units in navigating complex regulatory landscapes and ensuring compliance...
-
Regulatory Affairs Associate
il y a 2 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob Title: Associate Regulatory AffairsAbout the Role:We are seeking a highly skilled Associate Regulatory Affairs professional to join our team in Paris. As a key member of the Regulatory Affairs department, you will play a crucial role in supporting our business units in navigating complex regulatory landscapes.Key Responsibilities:Monitor regulatory...
-
Scientific Translator Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinJob Title:Regulatory Affairs Officer / Linguistic Review CoordinatorJob Summary:We are seeking a highly skilled Regulatory Affairs Officer / Linguistic Review Coordinator to join our team. The successful candidate will be responsible for ensuring and coordinating the Linguistic Review for Centralized products of one of our key clients.Key...
-
Regulatory Affairs Associate
il y a 2 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinAbout the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our Regulatory Watchtower team in Paris. As a key member of our Regulatory Affairs department, you will play a critical role in supporting our business units in navigating complex regulatory landscapes.Key ResponsibilitiesMonitor regulatory publications and supervisory trends...
-
Regulatory Affairs Associate
il y a 2 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob Title: Associate Regulatory AffairsSGS Société Générale de Surveillance SA is seeking a highly skilled Associate Regulatory Affairs professional to join our team in Paris. As a key member of the Regulatory Affairs department, you will play a crucial role in supporting our various departments in navigating banking supervision and related...
-
Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at SGS Société Générale de Surveillance SA. The successful candidate will be responsible for scanning the regulatory landscape, analysing regulatory changes, and prioritising impact assessments and implementation of requirements.The ideal candidate will have a law...
Head of Global Labelling – Regulatory Affairs
Il y a 2 mois
Job Title: Head of Global Labelling – Regulatory Affairs
Job Type: Full time permanent position
Locations: UK, France, Germany, Ireland, Netherlands, Norway, and the United States of America (Remote)
Remuneration: Competitive salary and benefits package
Working for one of the industry's leading pharmaceutical companies, this is a fantastic opportunity to provide expert regulatory knowledge by providing regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and post market compliance, working closely with healthcare regulatory bodies globally.
In this role, you will lead and oversee global labelling strategy, operations, and compliance, including creation and maintenance of labelling documents; and in doing so bring about enterprise-level change to better meet the needs of a growing business.
You will be responsible for implementing and managing processes around labelling globally, overseeing labelling activities worldwide for marketed products, creating and maintaining Company Core Data sheets, and also providing strategic advice in the creation of target labelling for development products.
The key job responsibilities:
- Directly oversee and provide strategic and tactical advice for the maintenance and development of CCDS and local labelling deliverables for regulatory filings
- Chair cross-functional Global Labelling Committee and Labelling Working Groups to manage the decision-making process for labelling updates to established products
- Design and implement strategy for the creation of a dedicated Global Labelling function
- Develop, improve, implement and document best-in-class labelling processes, metrics and templates, including influencing stakeholders at all levels
- Lead development of labelling for products in all stages of development including creation of Target Product Labels
- Liaise with other Regulatory Affairs functions to ensure labelling updates are submitted and implemented
- Monitor consistency between local labelling documents and Company Core Data Sheets, and ensure exceptions are documented through standard process
- Provide strategic interpretations of labelling regulations and guidelines in a range of markets including US and EU
- Ensure compliance and performance of labelling processes in accordance with departmental KPIs
- Input into requirements for tools and systems required for the compliant management of labelling documents
The positions job requirements/qualifications:
- Minimum of a Bachelor's Degree, preferably in a Scientific or Life Sciences Discipline. A PhD is desirable but not a must.
- Significant Regulatory Affairs Labelling experience, including direct experience with CCDS, Core Product Information and local labelling in a range of markets including US and EU
- Demonstrates subject matter expertise in labelling and labelling governance
- A strategic labeller with expertise in both developing and marketed labels in global regions
- Experience leading labelling professionals and preferably a global labelling team.
- Experience with label development including TPP
- Experience developing, implementing and operating global labelling processes for a pharmaceutical company with worldwide product licences
Other areas of importance:
- Previous experience in a big pharmaceutical environment, with sound understanding of the complexities in this environment
- Strong interpersonal skills, ability to forge connections and to influence stakeholders at all levels, in all regions
- Ability to clearly explain labelling concepts to senior stakeholders and Regulatory Affairs colleagues globally
- Ability to identify problems and their solutions, as well as driving them to resolution, delegating where necessary to achieve results
- Ability to learn new technologies, tools and systems quickly – experience with Veeva RIM Submissions and Registrations Vault desired
This is an excellent opportunity to join a leading business going through a period of growth. This position is a very senior position within the business so will look for a hands on leader who has experience in all aspects of regulatory labelling for both developing and establishing products.
To apply for this position please reach out to
Please note you must hold the FULL right to work in the locations provided, this role does not provide job sponsorship or relocation.
Disclaimer: Due to an influx of applications, not every application can be provided feedback.