Contract duration: 1 year/Possible extension
Responsibilities:
Ensuring GMP-compliant documentation of the operating and production processes as well as their completion
Preparation, implementation and follow-up during internal or external inspections, as well as close cooperation with internal and external interfaces
Initiation and processing of risk analyses
Processing of QRM assessments
Initiation and processing of deviations, changes, processing of complaints and carrying out checks for completeness
Creation and updating of work regulations (SOPs) to ensure GMP-compliant operating and production processes
Coordination of higher-level GMP projects across departments
Must Haves:
Completed Bachelor's/Master's degree in the field of pharmaceutical manufacturing or a related field
Very good communication skills, both written and spoken in German and English
Min. 1-3 years of professional experience in pharmaceutical production, development, quality assurance and control or a related industry
A team-oriented mindset with a view to continuous improvement of processes and the ability to achieve constant performance at a high level in an ever-changing environment.
Knowledge and committed commitment to process improvements (e.g. lean production system) and agile management are an advantage
Interest in coaching and change management is an advantage
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