In this position, you will be responsible for reviewing batch records. These include cleaning logs, production documentation review, temperature reports, test procedures, raw data and logbooks. You will support batch release by ensuring the completeness of the documentation package. For clarifications and evaluations, you cooperate with the operations team as well as the responsible QA manager. Further, you will collect and evaluate KPI data on a regular basis. Writing and revising SOPs in your area of expertise is also part of your tasks.
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company
If you are interested then kindly send your resume to: firstname.lastname@example.org
You have a structured, precise and well-organized working attitude. Previous experience in a GMP regulated pharmaceutical / API industry is an advantage.
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