Emplois actuels liés à Regulatory Affairs Specialist - Paris, Île-de-France - Indegene
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our regulatory team, you will be responsible for ensuring the delivery of regulatory activities performed onsite in the Paris region.About usProductLife Group is a leading company in the pharmaceutical industry, and we are...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France DSM Temps pleinJob Title: Regulatory Affairs SpecialistJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at DSM. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements in the food industry.Key Responsibilities:Support with compliance checks and regulatory assessment of food...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinRegulatory Affairs SpecialistGroupe ProductLife is seeking a skilled Regulatory Affairs Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for coordinating activities for our clients and ensuring compliance with regulatory processes.Key Responsibilities:Provide guidance and support to clients on...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Philips Iberica SAU Temps pleinJob TitleSenior Regulatory Affairs SpecialistWe are seeking a highly skilled and experienced Senior Regulatory Affairs Specialist to join our team at Philips Iberica SAU. As a key member of our Regulatory Affairs team, you will be responsible for ensuring that our medical devices comply with all relevant safety and environmental policies and regulations.Key...
-
Regulatory Affairs Specialist
Il y a 2 mois
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistProductLife Group is seeking a highly skilled Regulatory Affairs Specialist to join our team in Paris region. As a key member of our project team, you will be responsible for ensuring the delivery of regulatory activities performed onsite.About UsProductLife Group is a leading company in the pharmaceutical industry, dedicated to...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France PEP-Therapy Temps pleinJob Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PEP-Therapy, a clinical-stage biotechnology company developing innovative targeted therapies in oncology.Key Responsibilities:Develop and implement regulatory strategies aligned with business objectives to facilitate timely approvals for...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our project team, you will be responsible for ensuring the delivery of regulatory activities performed onsite in the Paris region.About usProductLife Group is a leading company in the pharmaceutical industry,...
-
Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities performed onsite in Paris region.About usProductLife GroupResponsibilitiesUnder the responsibility of the regulatory coordinator of this project and in close collaboration with subsidiaries, production sites, CMC Regulatory Project...
-
Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities performed onsite in Paris region as part of a project for one of our Top Clients.About usProductLife GroupResponsibilitiesCoordination of the collection of information relating to regulatory requirements or the analysis of the...
-
Regulatory Affairs Specialist
il y a 2 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs Specialist We are seeking a Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our regulatory team, you will be responsible for ensuring the delivery of regulatory activities performed onsite in the Paris region. About us: Group 10 Responsibilities: Coordination of the collection of...
-
Regulatory Affairs Specialist DM
Il y a 2 mois
Paris, Île-de-France NEO2 Temps pleinJoin NEO2 as a Regulatory Affairs Specialist DMNEO2 is seeking a highly skilled Regulatory Affairs Specialist DM to join our team. As a Regulatory Affairs Specialist DM, you will be responsible for ensuring compliance with regulatory requirements and developing strategies to mitigate risks.Main Responsibilities:Obtain and maintain CE markingManage technical...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at SGS Société Générale de Surveillance SA. As a key member of our Regulatory Affairs team, you will play a crucial role in supporting our various departments in dealing with banking supervision and related regulations.The Regulatory Affairs team is responsible...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist 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 various departments in dealing with banking supervision and related regulations.The Regulatory Affairs team is responsible...
-
Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities performed onsite in Paris region. As part of a project for one of our Top Clients, you will be responsible for coordinating the collection of information relating to regulatory requirements or the analysis of the regulatory impact of...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinKey ResponsibilitiesAs a Regulatory Affairs Specialist at SGS Société Générale de Surveillance SA, you will be part of the Regulatory Affairs team, supporting various departments in dealing with banking supervision and related regulations. Your role will be to provide strategic advice and insight into the company's regulatory landscape, enabling us to...
-
Regulatory Affairs Specialist
il y a 4 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...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinJob DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at SGS Société Générale de Surveillance SA. As a key member of our Regulatory Affairs department, you will play a crucial role in supporting our various departments in dealing with banking supervision and related regulations.The Regulatory Affairs team is...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinJob DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Groupe ProductLife. The successful candidate will be responsible for ensuring compliance with regulatory requirements and providing guidance on regulatory matters.Key ResponsibilitiesProvide regulatory guidance and support to the teamEnsure compliance with...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinIn the context of a new project, we are seeking a Regulatory Affairs Specialist to join our teams in Paris.ResponsibilitiesDevelop and maintain regulatory dossiers and coordinate with cross-functional teams.Ensure compliance with European regulations (2017/745) and other regional requirements.Maintain technical files and ensure export compliance.Elaborate...
-
Senior Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France SGS Société Générale de Surveillance SA Temps pleinWe are seeking a Senior Regulatory Affairs Specialist to join our Paris-based office. The successful candidate will support the Regulatory Affairs team in ensuring strategic alignment with regulatory topics. Key responsibilities include updating senior management on key regulatory publications and trends, informing senior management on regulatory changes,...
Regulatory Affairs Specialist
Il y a 2 mois
We are a technology-led healthcare solutions provider, driven by our purpose to enable healthcare organizations to be future-ready. Our team is passionate about creating leaders of tomorrow and nurturing them as people managers and account managers.
As a Regulatory Affairs Consultant, you will work with our material review team to support our engagement with medical device client partners and serve as a consultant to assist as an MLR SME (especially on medical device promotion regulations) on a medical device project.
Key Responsibilities:- Provide expert France Medical Device Promotion related Regulatory advice to the Indegene team with direct or indirect involvement in the client project, ensuring the client project requirements are met.
- Provide guidance on standards pertaining to advertising and promotion of medical devices in the France (and if possible, in EU and global regions).
- Provide guidance on France Regulatory Requirements for promotional material review for medical devices.
- Provide guidance on review workflow for medical device promotional materials for France market.
- Provide strategic input and guidance on regulatory affairs matters, including understanding the collaboration between global and local markets for medical device promotional materials and associated review workflow for repurposing content, understanding regulatory submission guidelines, filing, negotiations, and amendments, which includes obtaining, assessing and summarizing scientific and other technical information specific for France market.
- Life science graduate/post-graduate.
- Regulatory Affairs/Compliance professional with experience in Medical Device regulations and standards for device promotion and scientific communication, with 2 years' experience in review and approval of medical device promotional and non-promotional materials.
- Strong foundation in medical device regulatory affairs, with a total of 2-3 years working with a range of medical devices (Class 2 and above is preferred).
- Has experience with and understands Germany, EU and global medical device regulations.
- Ability to build and maintain strong and collaborative working relationships with internal and external contacts.
- Ability to analyse complex regulatory issues, propose effective solutions, and make sound recommendations to stakeholders.
We are an Equal Opportunity Employer and are committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics.
