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Found 30 jobs
    • Wavre
    • Negotiable
    • Posted about 23 hours ago

    Do you have a first experience in Regulatory Affairs, especially within the pharmaceutical industry? Are you looking for the next step in your career? Then this great opportunity as RA registration Manager might be your next challenge ! Job Description The Regulatory Affairs Registration Manager ...

    • Utrecht
    • €4000 - €5500 per month
    • Posted 1 day ago

    Do you have a proven track record as a scientist and/or project manager in the field of preclinical immunology, with a finished PhD or Post-Doc? Are you familiar with immunological assays, infectious diseases, vaccinology, and other similar immunological expertises? We are looking for a scientist...

    • Leiden
    • €4.200 - €5.000 per month
    • Posted 4 days ago

    Are you an expert in analytical development using HPLC / UPLC and are you looking for the next step in your career? We are looking for a Scientist (master / PhD) analytical development, who will help develop new methodologies to support the growing team in a pharmaceutical setting. Job Descriptio...

  • CRA
    • Diegem
    • Negotiable
    • Posted 8 days ago

    Do you have clinical research experience, good communication skills, a good mastery of Dutch, French and English ? A special interest in cardiology ? Then check out the position below, an exciting international CRA opportunity in the dynamic world of medical devices. Job Description This individu...

    • Beerse
    • Negotiable
    • Posted 17 days ago

    Do you have a solid experience in CMC Regulatory Affairs, and are you looking forward to a long-term mission with broad responsibilities ? At a global pharma company ? Then this is a great opportunity for you! Job Description You will be CMC Regulatory Affairs responsible for one or more commerci...

    • Maastricht
    • €3000 - €6000 per month + -
    • Posted 18 days ago

    For one of our internationally renominated clients in Life Sciences located in Limburg we are looking for a scientist with experience with validation process assessment. Do you have extensive experience with process validation and are you familiar with cell therapies and manufacturing under GMP c...

    • Switzerland
    • Up to US$0.00 per year
    • Posted 21 days ago

    Job Description: The Manufacturing Associate performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and fa...

    • Alkmaar
    • €4500 - €7000 per month + depending on your experience
    • Posted 21 days ago

    Voor onze klant, een producent van nucleaire geneesmiddelen zijn wij op zoek naar een manager voor de afdeling Release. Hiervoor zijn wij op zoek naar een echte peoplemanager! Functieomschrijving Als manager Certification and Release zul je leiding geven aan ongeveer 12 QP-ers. Verder ben je betr...

    • Flemish Brabant
    • Negotiable
    • Posted 23 days ago

    Do you have a solid scientific background (knowledge of cardiology is a big asset) and looking forward to an opportunity in Medical Affairs? Are you trilingual, enthusiastic and a good communicator ? Then you may be the candidate for the open MSL role at our client. Job Description Field-based sc...

    • Flemish Brabant
    • Negotiable
    • Posted 23 days ago

    Do the words enthusiastic, eager to learn and teamplayer describe you well ? Does the MSL role appeal to you, the contacts, the variety, the dynamism of the job ? Are you are trilingual with a good scientific background (ideally with some knowledge of immunology or dermatology), then check out th...

    • Brussels
    • Negotiable
    • Posted 25 days ago

    "Do you have a clinical or biomedical MSc/BSc with at least 4 years of relevant experience (preferentially working in a lab with clinical samples)? Do you want to act as the HQ expert at practical implementation of Translational Research and operationalize the policies and procedures that warrant...

    • England
    • Negotiable
    • Posted 28 days ago

    Do you have experience in designing, planning and conducting clinical trials within IVD? Are you available to work fulltime for one of the most successful biotech companies? Let's connect for this existing opportunity! Job Description Our client is looking for a clinical project manager who could...