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Irfa******
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United States
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Last Update: 01.11.2018 at 12:00
Job Type
Full Time
Start
ASAP
Duration
12 Month +
Place
Anywhere
Country
United States
Category
Regulatory, Quality and Clinical
Description
Key responsibilities:
Participate in internal projects as a representative for the Validation department
Prepare qualification/validation documents
Execute qualification tests
Review and approve validation documents
Prepare SOPs
SWEDISH SPEAKING
Key Skills/Experience/Requirements:
- M.Sc. or B.Sc. in Engineering or equal.
- At least 2 years GMP-experience from the Life Science Industry
- Experience in qualification activities for process equipment
Job Details
Seniority Level
Mid-Senior level
Industry
Pharmaceuticals Logistics