Regulatory Affairs Specialist – MedTech Devices

2 settimane fa


Padova, Italia Alchimia Srl A tempo pieno

A leading medical device manufacturer in Padova is seeking a Regulatory Affairs Associate. This role involves managing international product registrations, ensuring compliance with relevant regulations, and maintaining technical documentation. The ideal candidate should have a degree in a scientific discipline and prior experience in Regulatory Affairs. Excellent English communication skills and attention to detail are essential. This position offers a dynamic working environment with opportunities for career growth.#J-18808-Ljbffr


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    Padova, Italia Stevanato Group A tempo pieno

    A leading medical device company in Italy is seeking a Regulatory & Scientific Affairs Specialist. The candidate will manage regulatory processes, prepare documentation, and ensure compliance with standards in the healthcare industry. Candidates should have 2-5 years of experience in regulatory affairs or quality assurance in pharmaceuticals or medical...

  • Regulatory Affairs

    3 settimane fa


    Padova, Italia Stevanato Group A tempo pieno

    A leading medical device company in Italy is seeking a Regulatory & Scientific Affairs Specialist. The candidate will manage regulatory processes, prepare documentation, and ensure compliance with standards in the healthcare industry. Candidates should have 2-5 years of experience in regulatory affairs or quality assurance in pharmaceuticals or medical...


  • Padova, Italia Alchimia Srl A tempo pieno

    A leading medical device manufacturer in Padova is seeking a Regulatory Affairs Associate. This role involves managing international product registrations, ensuring compliance with relevant regulations, and maintaining technical documentation. The ideal candidate should have a degree in a scientific discipline and prior experience in Regulatory Affairs....


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    Regulatory Affairs Specialist needed to prepare and maintain technical documentation, support certification processes, and ensure regulatory compliance.


  • Padova, Italia Alchimia Srl A tempo pieno

    The Regulatory Affairs Associate will support product registrations and regulatory compliance.They will manage documentation, communicate with authorities, and ensure medical devices meet international standards.


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    Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in the fields of chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves.Since our foundation in ****, all our products have been...


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  • Padova, Italia Altro A tempo pieno

    We are looking for a Regulatory & Scientific Affairs Specialist to join our team in Italia (Piombino Dese). The chosen candidate will be responsible for or performing the regulatory intelligence process and regulatory and standard assessments, arranging registration dossier of medical devices, drug device combinations and drug container systems as well as...


  • Padova, Italia Stevanato Group A tempo pieno

    We are looking for a Regulatory & Scientific Affairs Specialist to join our team in Italia (Piombino Dese). The chosen candidate will be responsible for or performing the regulatory intelligence process and regulatory and standard assessments, arranging registration dossier of medical devices, drug device combinations and drug container systems as well as...


  • Padova, Italia Alchimia srl A tempo pieno

    Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in the fields of chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves. Since our foundation in 1993, all our products have been...