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Contract GMP Consultant/QA Specialist/Denmark/5 Months +

Eingestellt von Real Staffing Group

Gesuchte Skills: Consultant

Projektbeschreibung

Leading Medical Devices company are urgently looking for a Contract Process Validation Consultant with expertise in GMP for 5 months to perform process validation of the client's antibody production at their site in Denmark.

Tasks:- * Review general biological production techniques and methods, especially protein purification (chromatographic systems), protein conjugation and antibody fractioning

* Validate and review existing systems, documentation and SOPs

* Participate in quality audits and enhance quality management systems

* Lead the activities within the area

Experience:- * 5 years or more experience within production for Pharmaceutical or Medical Devices companies in a GMP regulated environment

* Process validation of production methods in a regulated environment

* Process documentation for biological production techniques (GMP)

* Fluent English, knowledge of a Nordic language would be beneficial bot not essential

Rate: Negotiable (depending upon experience)

Location: Denmark

Duration: 5 Months (extension possible)

Projektdetails

  • Einsatzort:

    København, Dänemark

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Organisation/Management

  • Skills:

    consultant

Real Staffing Group