TRD QA Quality Specialist

Posted 23 December 2021
Job type Limited
DisciplineLife SciencesQuality Assurance/Safety

Job description

For our customer a Pharmaceutical Company in Basel we are looking for a

TRD Quality Specialist

Job Purpose:

Support the QA Ops team in the timely release of GMP relevant documents. Support objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with GMP in TRD.

Major Activities:

  • Perform review of GMP relevant documents (e.g. manufacturing master documents, executed batch records for material manufactured internally or at contractors, raw data).
  • Clarify simple deficiencies in GMP documents with the line unit experts in own responsibility.
  • Upload GMP documents into relevant quality electronic systems (e.g. DocStore Condor, iRelease)
  • Write and complete GMP relevant documents in own area of responsibility (e.g CoAs, archiving checklists).
  • File and archive documents owned by QA Operations.
  • Collaborate with other associates to support the function of QA Ops.
  • Participate in knowledge exchange in TRD.


  • Bachelor degree or apprenticeship in chemistry (or any other equivalent scientific education)
  • Must have is relevant GMP experience in a pharmaceutical environment, ideally in the field of quality
  • Languages: fluent in English and German
  • Soft skills: team-oriented, reliable, motivated, attention to detail TRD QA Quality Specialist

Workplace: Basel

Workload: 100%

Working Time: flexible working hours

Start Date: 03.01.2021

Duration: 12 months

Your Application

Please apply online. For further information about the position, please contact your Kelly recruiter, Mr Franck Maerky (+41 61 270 80 17).