Quality Control (m/f)

Hesse  ‐ Onsite
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Description



Quality Control (m/f)

Reference: -en
Start: asap
Duration: 6 MM

Main tasks:
  • Expert role building bridge between analytical lab (conducting of analytical activities) and project activities
  • Conduction of Analytical method validation and Analytical method transfer from development to production
  • Preparation of source documents for MAA/NDA


Main qualifications
  • QC experience for development projects, especially for late stage phase of new active substances (NCE)/ tablet formulation
  • Fundamental GMP understanding (bench and prinicpal scientist activities)
  • Excellent knowledge on requirements (ICH, EMA, Japan submission) for analytical method validation, specifications, stability testing, PPQ
  • Expertise in key methods: UHPLC; Karl-Fisher, dissolution
  • Fluent English and German (written and spoken)


Main advantages:
    A very renowned company



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Silvia Charro Lopez

Referencenumber:


Make contact:
Email:
Start date
ASAP
Duration
6 MM
From
Hays AG
Published at
20.06.2018
Contact person:
Kerstin Werner
Project ID:
1578051
Contract type
Freelance
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