Regulatory Affairs Specialist
1 mese fa
Regulatory Affairs Specialist About the role Are you interested in a Regulatory Affairs role in a dynamic, fast and flexible Company?
This role will provide YOU the opportunity to lead key activities to progress YOUR career, joining a collaborative team of regulatory professionals.
Your responsibilities include some of the following: Manage preparation of new regulatory documents, dossiers and applications to enable products to be launched and maintained in market, with the correct alignment and compliance to regulations, proactively seeking innovative and rapid path to market medicinal products, medical-devices, cosmetics and food supplements.
Support the development of the strongest claims/advertising and promotion possible within the regulations, ensuring risks are appropriately addressed and communicated, and obtain the required authorizations where necessary.
Analyse regulatory issues and communicate with key stakeholders.
Work together to help develop plans to mitigate, so that we can deliver science that is robust and aligned with business needs.
Support key processes related to CMC, quality, labelling, artworks and local regulations.
Actively contribute to high-performing local teams, seeking continuous performance improvement.
Maintain required regulatory compliance databases, systems and processes.
Maintain high level of knowledge on the science of products within defined portfolio.
Qualifications Skills Relevant previous experience of at least 3 years in a pharmaceutical/healthcare company, preferably multinational.
Good knowledge of pharmaceutical laws and regulation and fluent management of the life cycle management.
Knowledge of the fundamentals of cosmetic, medical devices and food supplement laws and regulations.
Scientific Degree (Pharmacy, Pharmaceutical chemistry, Chemistry or related disciplines).
Master in Regulatory Affairs is preferred.
Fluent in English.
Ability to use Microsoft Word, Excel, PowerPoint and Adobe.
Preferred Good team player, with strong interpersonal skills to work well in cross-functional teams.
Works with a spirit of continuous improvement and innovation, creatively open to new ideas and methods.
Results-driven mindset, with the ability to work in a fast-paced, dynamic environment.
Good attention to detail and problem-solving skills within a structured process.
Organizational and time management skills, with ability to manage multiple priorities and meet tight deadlines.
Diversity, Equity and Inclusion At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.
We believe in an agile working culture for all our roles.
If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
#J-18808-Ljbffr
-
Regulatory Affairs Specialist
3 giorni fa
Milano, Lombardia, Italia Lights on Women (LoW) A tempo pieno{"title": "Regulatory Affairs Specialist", "content": "About the Role:Lights on Women (LoW) is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will play a crucial role in ensuring our compliance with EU regulatory requirements and supporting our business functions in the assessment of...
-
Regulatory Affairs Specialist
3 giorni fa
Milano, Lombardia, Italia Lights on Women (LoW) A tempo pienoJob Title: Regulatory Affairs SpecialistAt Lights on Women (LoW), we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will play a crucial role in ensuring our compliance with EU regulatory requirements and supporting our business functions in the gas distribution market.Key...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoJob SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Page Personnel. As a key member of our regulatory team, you will be responsible for managing and preparing regulatory dossiers for submissions of human drug substances to various regulatory authorities.Main ResponsibilitiesManage and prepare regulatory dossiers (CTD)...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoJob SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Page Personnel. As a key member of our regulatory team, you will be responsible for managing and preparing regulatory dossiers for submissions of human drug substances to various regulatory authorities.Main ResponsibilitiesManage and prepare regulatory dossiers (CTD)...
-
Regulatory Affairs Specialist Eu
3 mesi fa
Milano, Italia Clinglobal Group A tempo pieno**Regulatory Affairs Specialist - European Union** Clinglobal is an Animal Health Contract Research Organisation and supports our global operations in various countries. We are currently looking for a** Regulatory Affairs Specialist** based in the EU to join our growing Regulatory Affairs team at Clinglobal. This position offers the opportunity to work...
-
Regulatory Affairs Specialist
3 giorni fa
Milano, Lombardia, Italia CooperCompanies A tempo pienoJob Title: Senior RA SpecialistCooperVision is a leading manufacturer of soft contact lenses with a global presence. We're seeking a highly skilled Senior Regulatory Affairs Specialist to join our team.About the Role:As a Senior RA Specialist, you will provide regulatory support, guidance, and direction to products from concept to launch. You will follow the...
-
Regulatory Affairs Specialist
5 giorni fa
Milano, Lombardia, Italia PharmaLex A tempo pienoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PharmaLex. As a key member of our team, you will be responsible for managing the creation and maintenance of labelling and regulatory documentation for our clients.Key ResponsibilitiesParticipate in the preparation and revision of labelling and regulatory...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia PharmaLex A tempo pienoJob Title: Regulatory Affairs Specialist - LabellingPharmaLex is seeking a highly skilled Regulatory Affairs Specialist - Labelling to join our team. In this role, you will be responsible for ensuring the accuracy and compliance of labelling documentation for pharmaceutical products.Key Responsibilities:Participate in the preparation and revision of...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia PharmaLex A tempo pienoJob Title: Regulatory Affairs Specialist - LabellingPharmaLex is seeking a highly skilled Regulatory Affairs Specialist - Labelling to join our team. In this role, you will be responsible for ensuring the accuracy and compliance of labelling documentation for pharmaceutical products.Key Responsibilities:Participate in the preparation and revision of...
-
Regulatory Affairs Specialist
3 giorni fa
Milano, Lombardia, Italia PharmaLex A tempo pienoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PharmaLex. As a key member of our team, you will be responsible for managing the preparation and revision of informative texts for healthcare professionals and patients, as well as ensuring compliance with regulatory requirements.Key ResponsibilitiesParticipate in...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Page Personnel. As a key member of our team, you will be responsible for managing and preparing regulatory dossiers for submissions of human drug substances to various regulatory authorities.Main Responsibilities:Managing and preparation of regulatory dossier...
-
Regulatory Affairs Specialist
3 mesi fa
Provincia di Milano, Lombardia, Italia Instrumentation Laboratory spa A tempo pienoFor our Clinical Chemistry Strategic Business Unit, based in Milan (Italy), we are looking for a: **Regulatory Affairs Specialist - Maternity Leave**: The Regulatory Affairs Specialist handles the Regulatory Affairs activities in the pre-market. The main accountabilities of the Regulatory Affairs Specialist are: Support registrations, understand the local...
-
Regulatory Affairs Specialist
3 mesi fa
Milano, Italia AstraZeneca A tempo pieno**Regulatory Affairs Specialist (maternity leave)** At AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As **Regulatory Affairs Specialist (maternity leave)** in...
-
Regulatory Affairs Specialist
1 mese fa
Milano, Italia Haleon A tempo pienoRegulatory Affairs SpecialistAbout the role Are you interested in a Regulatory Affairs role in a dynamic, fast and flexible Company? This role will provide YOU the opportunity to lead key activities to progress YOUR career, joining a collaborative team of regulatory professionals. Your responsibilities include some of the following: Manage preparation of new...
-
Regulatory Affairs Specialist CIS
3 giorni fa
Milano, Lombardia, Italia Perfetti Van Melle A tempo pienoMain Purpose of the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our Group Regulatory Affairs Team in Italy. The successful candidate will be responsible for managing our product portfolio for the CIS countries, ensuring compliance with food and labeling regulations, and providing expert advice to support business growth.Key...
-
Senior Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia CooperCompanies A tempo pienoAbout the RoleWe are seeking a highly skilled and experienced Senior Regulatory Affairs Specialist to join our team at CooperCompanies. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.Key ResponsibilitiesRegulatory Support and Guidance: Provide...
-
Senior Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia CooperCompanies A tempo pienoAbout the RoleWe are seeking a highly skilled and experienced Senior Regulatory Affairs Specialist to join our team at CooperCompanies. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.Key ResponsibilitiesRegulatory Support and Guidance: Provide...
-
Regulatory Affairs Analyst/specialist
3 mesi fa
Milano, Italia Axpo Italia SpA A tempo pienoAxpo è guidata da un unico scopo: consentire un futuro sostenibile attraverso soluzioni energetiche innovative. Axpo è il più grande produttore di energia rinnovabile della Svizzera e un leader internazionale nel commercio di energia e nella commercializzazione di energia solare ed eolica. Axpo unisce l'esperienza e la competenza di oltre 5.000...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia PharmaLex A tempo pienoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PharmaLex. As a key member of our team, you will be responsible for managing the preparation and revision of informative texts for healthcare professionals and patients, as well as ensuring compliance with regulatory requirements.Key ResponsibilitiesParticipate in...
-
Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia PharmaLex A tempo pienoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PharmaLex. As a key member of our team, you will be responsible for managing the preparation and revision of informative texts for healthcare professionals and patients, as well as ensuring compliance with regulatory requirements.Key ResponsibilitiesParticipate in...