Position: Entry level

Job type: Full-time

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Job content

Responsibilities
  • GMP-compliant approval decisions for dosage forms (bulk, Biotech DS) according to the product range of the internal process unit, as well as external manufacturers (CMOs)
  • GMP-compliant assessment and decision on deviation reports (AWMs) for dosage forms (bulk and finished product), with escalation according to SOP
  • Ensuring the correct and timely creation and dispatch of Certificates of Analysis (CoAs)
  • Active tracking of deadlines with regard to approval and escalation in the event of any delays
  • Participation in the preparation of annual reports
Qualifications
  • University degree in chemistry / pharmacy / biology / medicine
  • Good language skills in German and English
  • Prior knowledge in the pharmaceutical environment is desirable
Have we picked your interest?

Then send us your updated CV by email at jtoma@aerotek.com.

We are looking forward to meet you!
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Deadline: 10-05-2024

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