Lavori attuali relativi a Regulatory Affairs Specialist - Milano, Lombardia - Recordati

  • Regulatory Affairs Expert

    1 settimana fa

    Milano, Lombardia, Italia Flamma spa A tempo pieno

    Job Title:Corporate Regulatory Affairs SpecialistAbout Us:Flamma Group is a leading pharmaceutical company specializing in the development, production, and commercialization of active pharmaceutical ingredients (APIs) and molecules.Job Overview:We are seeking an experienced Corporate Regulatory Affairs Specialist to join our team in Chignolo d'Isola, Italy....

  • Regulatory Affairs Specialist: Global Compliance Expert

    4 settimane fa

    Milano, Lombardia, Italia Healthcare Businesswomen'S Association A tempo pieno

    Healthcare Businesswomen'S Association is a leader in the Generic and Biosimilar medicines sector, touching the lives of almost 500 million patients annually. We're now seeking a skilled Regulatory Affairs Specialist to join our team and play a crucial role in shaping the future of our organization.**Job Summary:**We are looking for an experienced Regulatory...

  • Regulatory Affairs Specialist for EU Compliance

    3 giorni fa

    Milano, Lombardia, Italia Clinglobal Group A tempo pieno

    Company OverviewClinglobal Group is a leading Animal Health Contract Research Organisation that supports its global operations in various countries. Our company offers the opportunity to work remotely with occasional visits to our offices and partner companies' premises as required.Job DescriptionWe are currently seeking a Regulatory Affairs Specialist based...

  • Regulatory Affairs Professional for Medical Devices

    3 settimane fa

    Milano, Lombardia, Italia Page Personnel A tempo pieno

    Page Personnel is seeking a highly skilled Regulatory Affairs Specialist to play a key role in ensuring compliance with regulatory requirements for our medical devices. The ideal candidate will have a strong understanding of FDA regulations, EU Medical Device Regulation (MDR), and international regulatory requirements for medical devices.About the RoleWe are...

  • Regulatory Affairs Expert

    3 settimane fa

    Milano, Lombardia, Italia Flamma spa A tempo pieno

    About Flamma spa">Flamma spa is a leading pharmaceutical company specializing in the development, production, and commercialization of molecules and active pharmaceutical ingredients (APIs). With headquarters in Chignolo d'Isola, Italy, near Milan, Flamma has two production sites in Italy, one in Isso (BG) and one in Bulciago (LC), as well as two...

  • Regulatory Affairs Professional

    3 settimane fa

    Milano, Lombardia, Italia Reckitt A tempo pieno

    About the RoleAs a Regulatory Assistant, you will be at the forefront of our innovation and compliance efforts. You will jumpstart your career in a role that provides a blend of strategic thinking and hands-on experience within a dynamic, collaborative environment.We are seeking a highly motivated and detail-oriented individual to join our Regulatory team....

  • Regulatory Affairs Specialist for EU Oncology Portfolio

    3 settimane fa

    Milano, Lombardia, Italia Pfizer A tempo pieno

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team and lead the development of regulatory strategies for our early-stage oncology portfolio in the EU region.About the RoleProvide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST)Lead and implement EU regulatory strategies in...

  • Senior Regulatory Affairs Director

    3 settimane fa

    Milano, Lombardia, Italia Cpl Healthcare A tempo pieno

    Job Title:Senior Regulatory Affairs Director - Medical Device Lifecycle ManagementLocation:Italy (Milan) – HybridAbout the Role:This is an exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to increasing growth, the business is looking for an Associate...

  • Regulatory Affairs Professional

    3 settimane fa

    Milano, Lombardia, Italia Pfizer A tempo pieno

    **About the Role**Pfizer is seeking a highly skilled Regulatory Affairs Professional to join our team in the Early Phase Oncology department. This role will be responsible for ensuring timely submissions and approvals in the EU region, as well as providing regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST).Key...

  • Head of Medical and Regulatory Affairs for Italy

    3 settimane fa

    Milano, Lombardia, Italia Ipsen Spa A tempo pieno

    About the RoleWe are seeking an experienced Head of Medical and Regulatory Affairs to lead our medical and regulatory affairs activities in Italy. As a key member of our leadership team, you will be responsible for ensuring that all medical and scientific support activities are conducted with the highest level of quality and compliance.Key...

  • Regulatory Affairs Expert for Global Pharmaceutical Development

    3 settimane fa

    Milano, Lombardia, Italia Pfizer, S.A. de C.V A tempo pieno

    Job Description:Pfizer, S.A. de C.V seeks a skilled Regulatory Affairs Expert to support the development and approval of innovative medicines. The ideal candidate will possess in-depth knowledge of global regulatory environments, with a focus on EU regulations. Key responsibilities include providing strategic regulatory guidance, leading/co-leading projects,...

  • Global Compliance Specialist

    1 settimana fa

    Milano, Lombardia, Italia Flamma spa A tempo pieno

    About Flamma Group:We are a global pharmaceutical company with a strong presence in the European market. Our Headquarter is located in Chignolo d'Isola, near Milan, Italy, with additional production sites in Isso (BG), Bulciago (LC), Philadelphia (USA), and Dalian (China).Job Description:We are looking for a highly skilled Corporate Regulatory Affairs...

  • Global Regulatory Strategy Expert

    3 settimane fa

    Milano, Lombardia, Italia Pfizer A tempo pieno

    Pfizer is a Patient-Centric CompanyWe're looking to bring medicines to the world faster, and we're not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and...

  • Global Medical Affairs Team Lead

    1 settimana fa

    Milano, Lombardia, Italia Shockwave Medical, Inc. A tempo pieno

    About the RoleThe Medical Affairs Senior Specialist - International plays an integral role in supporting the International Medical Affairs team.Job Summary:This position provides project and operational management to support the strategic planning and tactical execution of International medical affairs projects, and the investigator sponsored research (ISR)...

  • Regulatory Compliance Specialist

    4 giorni fa

    Milano, Lombardia, Italia Ipsen Spa A tempo pieno

    About the Role">Ipsen Spa, a dynamic and growing global specialty-driven biopharmaceutical company, is seeking a highly skilled Regulatory Compliance Specialist to join our team. With a strong focus on innovation and specialty care, Ipsen aims to make a sustainable difference by improving patients' health and quality of life.As a Regulatory Compliance...

  • Esperto di Affari Regolatori

    2 settimane fa

    Milano, Lombardia, Italia Direzione Lavoro A tempo pieno

    Descrizione del LavoroNel ruolo di Regulatory Affairs Specialist, si ricerca una risorsa da inserire nel REGOLATORIO come Regulatory Affairs. La responsabilità principale consiste nell'implementare i processi al fine di ottenere e mantenere l'autorizzazione alla commercializzazione dei prodotti a supporto dei piani aziendali globali.Compiti...

  • Corporate Affairs Specialist

    3 settimane fa

    Milano, Lombardia, Italia Pirelli A tempo pieno

    Pirelli, a leading global brand in the tyre industry, is seeking an experienced Corporate Affairs Specialist to join its Corporate Affairs & Governance function. The successful candidate will have a strong background in corporate law and governance, with excellent analytical skills and stakeholder management.Job Description:The role involves organizing and...

  • Regulatory Compliance Specialist

    4 giorni fa

    Milano, Lombardia, Italia Reckitt A tempo pieno

    About the Role:">As a Regulatory Compliance Specialist, you will be responsible for ensuring that our consumer products meet global standards and comply with local regulations. This is an exciting opportunity to join our team and contribute to the development of safe and effective products for our customers.">Your Key Responsibilities:">- Support the...

  • Regulatory Operations Associate Specialist

    4 giorni fa

    Milano, Lombardia, Italia Randstad Italia Spa A tempo pieno

    OverviewRandstad Inhouse Services, a specialty Pharma provider, is seeking a skilled resource to join the regulatory team as a Contractor Regulatory Operations Associate. This role is based in Milan and involves working with External Supply Quality (ESQ) managed contractors.

  • Responsabile dei Processi Regolatori per Prodotti Biomedici

    2 settimane fa

    Milano, Lombardia, Italia Antal International Network A tempo pieno

    Regulatory Affairs Manager - Antal International Network è alla ricerca di un Regulatory Affairs Manager per lavorare per un importante cliente nel settore chimico-farmaceutico. Il candidato ideale avrà una laurea in discipline scientifiche e almeno 5 anni di esperienza nel campo dei dispositivi medici. Sarà responsabile della gestione dei processi...

Regulatory Affairs Specialist

2 mesi fa

Milano, Lombardia, Italia Recordati A tempo pieno
Job Description

Recordati is seeking a highly skilled Regulatory Affairs Specialist to join its international team. As a key member of the Corporate Regulatory Affairs department, you will be responsible for the management of regulatory activities for medicinal products for human use.

Key Responsibilities:

  • Preparation, review, and submission of relevant documentation to regulatory authorities
  • Management of data and documentation in electronic systems
  • Cooperation with cross-functional teams to determine and manage timelines for regulatory filings
  • Participation in the management of core dossiers, including gap-analysis activities
  • Maintenance of relations with regulatory authorities and monitoring of legislation in force

Requirements:

  • Scientific degree in Regulatory Affairs
  • 4-5 years of experience in regulatory affairs within multinational pharmaceutical firms or international regulatory consulting companies
  • High level of autonomy and strong work ethic
  • Excellent communication and collaboration skills

About Recordati:

We are a global pharmaceutical force with over 4,300 employees, committed to creating a diverse environment and cultivating a culture of inclusion.

We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer, recruiting, developing, and rewarding without regard to various factors.