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beBeeRegulatoryAffairs

Lavori di beBeeRegulatoryAffairs in Italia

28 lavori presso beBeeRegulatoryAffairs in Italia

  • beBeeRegulatoryAffairs Rome

    Descrizione del ruolo: · Siamo alla ricerca di un Responsabile Regulatory Affairs per supportare il nostro team nella gestione dei dossier normativi nel settore alimentare e farmaceutico veterinario. Il candidato si occuperà della revisione e dell'aggiornamento delle linee guida, ...

  • beBeeRegulatoryAffairs Torino

    Regulatory Affairs Manager Job Description · Evaluate regulatory compliance of biocides and insecticides across markets to ensure alignment with industry standards. · Monitor European and national regulations (BPR, REACH, CLP), assessing business impact and identifying areas for ...

  • beBeeRegulatoryAffairs Cremona (CR)

    Job Title: Regulatory Affairs Specialist · Are you passionate about ensuring product compliance and supporting business growth? Do you have experience in cosmetic regulatory affairs? · We are seeking a detail-oriented and organized Regulatory Affairs Specialist to join our team. ...

  • beBeeRegulatoryAffairs Turin

    Job Overview · Olon Group is a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO and generic markets. · We prioritize international standards to integrate chemical synthesis and biological processes. · Our manufacturing sites ope ...

  • beBeeRegulatoryAffairs Vimercate (MB)

    Regulatory Affairs Professionals needed for EMEA region · Description: · We are seeking experienced professionals to join our Regulatory Affairs team in the EMEA region. As a key member of this team, you will be responsible for ensuring compliance with European regulatory requir ...

  • beBeeRegulatoryAffairs Firenze

    Job Title · A Regulatory Affairs Specialist role has become available within our Global Regulatory Affairs department. · ...

  • beBeeRegulatoryAffairs Ripalta Cremasca (CR)

    Job Role Overview: · We are seeking a diligent professional to ensure compliance with cosmetic laws and regulations by creating administrative documents. · The ideal candidate will perform regulatory checks following customers' banlist and international regulations. · This role i ...

  • beBeeRegulatoryAffairs Milano

    Regulatory Affairs Manager · We are seeking a Regulatory Affairs Manager to play a key role in regulatory compliance and support the development and market introduction of new products. · Ensure full compliance of our biocidal product portfolio across relevant markets. · Monitor ...

  • beBeeregulatoryaffairs Brescia

    Job Description: · We are seeking a proactive and enthusiastic professional to join our team as a Regulatory Affairs Specialist. As a key partner in product development and manufacturing, we strive for excellence in compliance with European regulations. · About the Role: · This f ...

  • beBeeRegulatoryAffairs San Daniele del Friuli (UD)

    Job Overview · We are seeking a seasoned professional to lead our Regulatory Affairs Intelligence Project Management initiatives. · This is an exciting opportunity for an experienced project manager to spearhead the development of strategic plans, ensuring compliance with regulat ...

  • beBeeRegulatoryAffairs Torino

    Our company offers a career in Regulatory Affairs. As a regulatory professional, you will be responsible for ensuring compliance with all relevant regulations and laws. · Key Responsibilities: · Evaluate new products and services to ensure they meet regulatory requirements · Anal ...

  • beBeeRegulatoryAffairs Turbigo

    A leading pharmaceutical company in Italy is seeking an RQS Manager to oversee the Regulatory Affairs strategy and Quality Management System. · Job Responsibilities: · Guide local teams · Evaluate compliance with safety standards · Interact with Health Authorities · ...

  • beBeeRegulatoryAffairs cremona

    Job Description · We are seeking a skilled Regulatory Affairs Specialist to join our team. The ideal candidate will have expertise in cosmetic regulations and be able to ensure compliance with current laws and regulations. · Main Responsibilities: · <ul style= ...

  • beBeeRegulatoryAffairs Bernareggio (MB)

    · AxL Spa – divisione Alti Profili, cerca un/una: · Senior Regulatory Affairs Specialist · Responsabilità principali · <ul style= ...

  • beBeeRegulatoryAffairs Rome

    Expertise in Regulatory Affairs is required to manage the CE certification of medical devices and ensure compliance with regulatory requirements throughout their lifecycle. · About This Opportunity · A Master's degree in health sciences or a related field is necessary for this ro ...

  • beBeeRegulatoryAffairs Turin

    Ruolo e responsabilità · Lavorare in un contesto interfunzionale, garantendo l'indipendenza di lavoro per assicurare la continuità delle attività operative. · Competenze richieste• Lavorare con indipendenza garantendola continuità delle attività operative. · Caratteristiche del r ...

  • beBeeRegulatoryAffairs Turin

    Regulatory Affairs Specialist · The Role Overview: · In this pivotal role, you will be responsible for ensuring the regulatory compliance of our biocides and insecticides portfolio across various markets. · Job Responsibilities: · Evaluate and interpret European and national regu ...

  • beBeeRegulatoryAffairs Ripalta Cremasca

    Job Description · The Finished Products Regulatory Affairs Specialist ensures the creation and administrative monitoring of all documents necessary for regulatory compliance with current cosmetic laws: · Perform regulatory checks following Customers Banlist and international regu ...

  • beBeeRegulatoryAffairs Siena (SI)

    Regulatory Affairs Specialist · We are seeking a highly motivated and qualified Regulatory Affairs Specialist to provide support in formulating and implementing regulatory strategies for the development of company products. · Lead and manage activities concerned with the submissi ...

  • beBeeRegulatoryAffairs Bresso (MI)

    Job Description · The CMC Senior Specialist plays a crucial role in ensuring the technical support for product registration dossier management and writing/reviewing the Quality Part of the CTD with internal/external resources. · ...