Regulatory submission Jobs

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  • Innerhalb der letzten 7 Tage  158
  • Head Of Corporate Regulatory Affairs & Cmc

    Bubendorf, Basel-Landschaft

    Support the elaboration, establishment, and application of the RA standard at all sites. Ensure internal standards for regulatory compliance of regulated...
    vor 3 Tage in Jobleads

    Melden
  • Global Head of Regulatory Affairs - Established Clinical...

    WhatJobs Zürich, Zürich

    Global Head of Regulatory Affairs. Established Clinical Stage Biotech. Switzerland Global Head of Regulatory Affairs. Established Clinical Stage Biotech...
    vor 2 Tage in Talent.com

    Melden
  • Product Stewardship & Regulatory – EMEA Chemical Management...

    DuPont Meyrin, Genf

    ...regulatory input to routine registration / license to sell questions. Represent DuPont with external parties including regulators (particularly EU ECHA)...
    vor 2 Tage in Talent.com

    Melden
  • Regulatory Reporting Specialist

    Swissquote Gland, Waadt

    Job Description As a Regulatory reporting specialist in the finance department, you will be part of a dynamic team in charge of the Group’s regulatory...
    vor 8 Tage in Talent.com

    Melden
  • Specialist Regulatory Reporting

    coni partner Zürich, Zürich

    ...candidates. Our client is an international private bank based in Zurich. We are looking for an accounting specialist (m, f, d) as Specialist Regulatory...
    vor 7 Tage in GermanPersonnel

    Melden
  • Senior Director Regulatory CMC Affairs

    BioTalent Switzerland

    ...Regulatory Affairs jobs in Switzerland. We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the...
    vor 8 Tage in Whatjobs

    Melden
  • Director, Medical Writing

    Morges, Waadt

    ...of the development of the clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission...
    vor 3 Tage in Jobleads

    Melden
  • Director, Medical Writing

    Incyte Biosciences International Sàrl Morges, Waadt

    ...of the development of the clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission...
    vor 2 Tage in LifeworQ

    Melden
  • Principal Scientist – Drug Product Process Development

    Schaffhausen, Schaffhausen

    ...regulatory submissions for biologics. Working knowledge of GMP and ICH guidelines applicable to drug product development. Comfortable working in matrixed...
    vor 3 Tage in Jobleads

    Melden
  • Associate Director Principal Writer I

    Incyte Morges, Waadt

    ...team environment. Proficient understanding and knowledge of global regulatory requirements needed and knowledge of therapeutic areas in all phases of clinical
    vor 3 Tage in LifeworQ

    Melden
  • Associate Director Principal Writer I

    Incyte Corporation Morges, Waadt  +1 Standort

    ...team environment. Proficient understanding and knowledge of global regulatory requirements needed and knowledge of therapeutic areas in all phases of clinical
    vor 4 Tage in LifeworQ

    Melden
  • Principal Medical Writer

    PRA Switzerland

    ...key phases, processes, and techniques of drug development from protocol development through submission. Excellent communicator and driver of cross-functional
    vor 4 Tage in Talent.com

    Melden
  • Medicinal Product Safety Scientist

    Basel, Basel-Stadt

    ...Regulatory bodies. Additional Responsibilities: Performs mentoring of Safety Scientist or related functions, as appropriate. Acts as MedDRA expert and...
    vor 3 Tage in Jobleads

    Melden
  • Senior Medical Writer

    neu PRA Switzerland

    ...of the authoring functions, facilitation of the review of the documents and ensuring that documents are submission-ready and finally approved. LI-Remote
    vor 1 Tag in Talent.com

    Melden
  • Nonclinical Scientific Writer

    F. Hoffmann-La Roche Gruppe Basel, Basel-Stadt

    ...regulatory and scientific functions across Roche to ensure comprehensive and accurate nonclinical dossiers are being submitted to HAs Work closely with...
    vor 4 Tage in LifeworQ

    Melden
  • Nonclinical Scientific Writer

    Basel, Basel-Stadt

    ...Manage the preparation, review, and submission of nonclinical summary documents for both early development and marketing applications Work with regulatory and
    vor 3 Tage in Jobleads

    Melden
  • R&D Engineer

    Lausanne, Waadt

    ...and detailed drawings using CAD software. Lead and support process validation activities, including IQ, OQ, and PQ, to ensure all processes meet regulatory...
    vor 3 Tage in Jobleads

    Melden
  • Materiovigilance & Complaints Specialist

    Rancate, Tessin

    ...events and complaints related to the company’s orthopedic products. This role involves ensuring the timely investigation of complaints, reporting to regulatory...
    vor 3 Tage in Jobleads

    Melden
  • Materiovigilance & Complaints Specialist (1818_94848)

    Rancate, Tessin

    ...events and complaints related to the company’s orthopedic products. This role involves ensuring the timely investigation of complaints, reporting to regulatory...
    vor 3 Tage in Jobleads

    Melden
  • Financial Reporting Analyst

    neu Citibank (Switzerland) Basel, Basel-Stadt

    ...regulatory reporting background is an advantage Knowledge of banking products and their accounting/reporting in IFRS is an advantage Advanced MS Excel...
    vor 1 Tag in Talent.com

    Melden
  • Global Safety Lead

    argenx Zürich, Zürich

    ...assigned products Develop and execute safety signaling and benefit-risk management strategies Closely collaborate with stakeholders internally (e... Regulatory...
    vor 2 Tage in LifeworQ

    Melden
  • Clinical Development Medical Director (CDMD) NS

    Novartis Basel, Basel-Stadt

    ...Clinical Development Medical Director (CDMD) is the Global clinical leader of defined and assigned program level activities and deliverables (e... submission...
    vor 2 Tage in LifeworQ

    Melden
  • Medicinal Product Safety Scientist

    Basel-Landschaft

    ...Regulatory bodies e... ISS, Reference Safety Information (RSI) section of Investigator Brochure (IB), EU Risk Management Plan (RMP) etc. As required...
    vor 3 Tage in Jobleads

    Melden
  • Senior Manager Programming (m/f/d)

    Fresenius Kabi Eysins, Waadt

    ...programming activities, including when outsourced to external partners. Provision of statistical programming expertise from clinical study set up to submission...
    vor 3 Tage in LifeworQ

    Melden
  • Global Safety Lead

    Argenx Bern, Bern

    ...assigned products Develop and execute safety signaling and benefit-risk management strategies Closely collaborate with stakeholders internally (e... Regulatory...
    vor 3 Tage in LifeworQ

    Melden

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Regulatory submission Jobs

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