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Scientist Clinical Immunology



Introductie

You will garantee the correct design and execution of experiments for the development, qualification and validation of immunological assays to be used in the analysis of samples from clinical trials. Are you an expert in immunology? Apply now!

Het bedrijf / The company

A international pharmaceutical company. This department is responsible for the immunological
evaluation of vaccine candidates in clinical trials.




De functie / The role

You will garantee the correct design and execution of
experiments for the development, qualification and validation of
immunological assays to be used in the analysis of samples from clinical
trials. Are you an expert in immunology? Apply now!


As Scientist Clinical Immunology you will garantee the correct design and execution of
experiments for the development, qualification and validation of
immunological assays to be used in the analysis of samples from clinical
trials. To do so, you:

  • Perform experiments on a regular basis to
    support assay development and maintain your technical edge by following relevant literature and
    knowledge in the field
  • Generate high-quality scientific reports to document your work
  • Are responsible for the long-term life cycle management of the methods, together with the key reagents, equipment and data
    analysis tools required for the assay to be performed
  • Your activities must be executed, documented and reported
    according to Good Clinical Laboratory Practice (GCLP) quality
    requirements
  • Furthermore, you are responsible for instructing associate and assistant scientist on the
    scientific fundamentals of the assays, and you will critically review the data generated by them


Het profiel / Your profile

For the position of Scientist Clinical Immunology we are looking for a candidate with at least 2 years of experience in industry within a pharmaceutical or biotech company

  • PhD in biological/medical sciences or equivalent, with strong immunology or virology background
  • Extensive hands-on experience in the development to validation of serology or cell based assays (ELISA, Virus Neutralization Assays, ELISPOT, Flow Cytometry or similar) according to regulatory standards (e.g. ICH)
  • Excellent skills in technical writing
  • Experience with using the "Design of Experiment (DoE)" principles is a plus
  • Knowledge of biostatistics, experience in statistical programs such as SPSS or JMP is a must
  • Experienced in working under quality standards such as GCLP, GCP or GMP is a plus
  • Excellent communication, coordinating and planning skills
  • As a person you are quality minded, flexible and you remain calm and positive under pressure. Furthermore you are a team player who is able to motivate others


Het aanbod / The offer

  • A contract for 12 months at CheckMark, with the possibility of an extension
  • Salary indication starting from €3600,- based on fulltime
  • Fulltime position (40 hours/week), 32 hours is discussable for candidates with relevant work experience


Reactie / Reaction

Neem voor meer informatie contact op met Sebastiaan Loriaux: 088 00 21 126
Vacaturenummer: 7184




Solliciteer hier
Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop

Uw referentie aan www.fmfvacatures.nl wordt gewaardeerd.
Your referral to www.fmfvacatures.nl is appreciated.


Gegevens

Werkgever:
CheckMark Labrecruitment
Vacaturesteller:
CheckMark Labrecruitment
Standplaats:
Regio Leiden

Geplaatst op FMF: 28 juli 2021

Branche: Farma & Biotech, Healthcare
Functie: R&D, QC / Laboratory
Vacatures Internationaal: Internationaal
Opleidingsniveau: HBO / BSc, WO/academisch / MSc
Werkervaring: 2-5 jaar, 5-10 jaar