Posição: Entry level

Tipo de empregos: Full-time

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Conteúdo do emprego

Proclinical are recruiting a QA Specialist Review/Release for a pharmaceutical corporation. This role is on a permanent basis and is located in Germany. The client is focused on changing the findings, developments, and productions of biologics through a thorough open-access platform.

Responsibilities
  • Assist with regulatory proposal documentation and be prompt for inspections.
  • Offer aid for planning regulatory proposals and actions to be prompt for inspection.
  • To ensure data integrity and offer direction from a QA perspective, which may involve deviation, CAPA, change control, qualification, etc., you will manage audit quality documents of functional divisions.
  • Aid in the release of raw material, IPC, equipment, rooms, utility, facility, etc.
  • You will discuss with client QA when required assisting with the release of bulk drug substance.
  • Other duties may be assigned to this role.
Key Skills And Requirements
  • Educated to a degree level in a technical or pharmaceutical field such as biochemistry, biology, chemistry, pharmacy, etc.
  • Familiarity with working in a biotechnology and/or pharmaceutical organisation in a quality role.
  • Capable of comprehending technical documentation.
  • Expertise on GxP needs and guidelines.
  • Acquaintance with assisting with internal audits would be preferable.
  • Works well in a team environment.
  • Communication skills both verbally and in writing.
  • Fluency in the English language with knowledge in German would be ideal.
If you are having difficulty in applying or if you have any questions, please contact Antoine Mortiaux at + 496950608631.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#QualityAssurance

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Data limite: 06-12-2024

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