Technical Writer - QC (m/f)

REFERENZNUMMER:

317539/11

IHRE AUFGABEN:

-Revision of existing test instructions and protocols of analytical methods
-Ensuring the compliance of analytical test methods with EHS, pharmacopeia and cGMP requirements
-Collecting and implementing stakeholder feedback for test methods instruction from scientific experts, EHS, QA and quality systems
-Revision of existing and writing of new SOPs for QC processes
-Ensuring the compliance of QC processes with global and local guidelines and procedures as well as with legal and regulatory requirements
-Collecting and implementing stakeholder feedback for QC process documents from EHS, QA and quality systems
-Translation of German documents into English and vice versa

IHRE QUALIFIKATIONEN:

-Knowledge of chemical, biochemical and microbiological analytical methods
-Knowledge of cGMP requirements for QC processes
-Laboratory experience in a cGMP regulated environment
-Excellent verbal and written skills in German and English
-Experience in using MS office software
-Experience in writing document standards and processes instructions
-Experience in using document management software
-Team player mentality and good communication skills, fluency in German and English

WEITERE QUALIFIKATIONEN:

Quality manager