One of the leading Biopharmaceutical CDMO's globally is looking to expand and add Porject Leader to the team. The business is currently growing massively which is largely down to significant investment into new product areas and drug lines. This means, joining the business now, can provide you with the opportunity to work internationally, on a diverse range of projects.
Your tasks :
Establishing and maintaining customer relationships
Preparation and support of production campaigns
Processing of change requests and deviations under GMP
Supervision of customer audits and inspections by authorities.
Calculate and monitor the QC costs in the project
Responsible coordination, prioritization and scheduling of tasks
Your qualifications :
Completed studies (MSc / BSc / Diploma) in the natural sciences (chemistry, biochemistry or pharmaceuticals) with 2 years of experience
Experience in the GMP environment and in quality control are an advantage
Good communication skills in German and English are required
Experienced handling of common software applications (MS Office, ...) is required,
user and / or specialist knowledge of individual pharmaceutical / laboratory software (e.g. Documentum, LIMS, Trackwise, ...) is an advantage
Good comprehension and very good organizational skills complete your profile.