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  Société
Fresenius Kabi AustriaLieu(x)
GrazSenior Manager Drug Product Process Development and Manufacturing (m/f/d), Graz
CDI
	
		  Industrie Pharmaceutique
Santé
Technique medical
	  
Santé
Technique medical
	  Ingénieur
Technicien
	
Technicien
Offre archivée le 08/07/2024
  Fresenius Kabi Austria
Fresenius Kabi Austria, with headquarters in Graz and a further production site in Linz, is a subsidiary of Fresenius Kabi AG, a world leading manufacturer of infusion therapy and clinical nutrition products. Fresenius Kabi Austria has 1600 employees and ranges among the top enterprises of the region.
Missions
- Oversee and guide drug product activities including drug product process development, technology transfer, process characterization and validation and submission of CMC documents to Regulatory Authorities
 - Define technical development that follows the principles of Quality by Design (QbD) and specify activities, milestones and costs
 - Drive issue resolution in order to achieve Biosimilarity within the pre-defined analytical similarity corridor with respect to drug product attributes
 - Provide scientific and technical operational guidance for drug product process development and manufacturing activities to the Biosimilars CMC team, Drug Product Process Development & Manufacturing Sites
 - Provide technical and scientific oversight of licensed biosimilar drug product processes to ensure consistency of supply
 - Build and sustain transparency with key internal and external stakeholders
 - Develop and maintain scientific expertise in Biosimilars development including up-to-date knowledge of relevant CMC regulatory guidelines and requirements
 
Profil
- Bachelor in pharmacy, biotechnology, biophysics, biochemistry or similar and PHD (pharmacy, biotechnology, biophysics, biochemistry or similar)
 - Minimum 8 years in pharmaceutical/biotech company specializing in drug product activities; preferably with at least part in a manufacturing setting. Previous experience working with biosimilars would be an advantage.
 - Strong knowledge of biologics with a focus on drug product process development and manufacturing activities
 - Good understanding of cGMP requirements, audits and HA interactions
 - Ability to operate in a global matrix organization with various functions
 - Skills in managing and influencing constructive interactions with key stakeholders across multiple cultures in a dynamic matrix environment
 - Very good spoken and written knowledge of English and German, French is a plus
 - Skilled problem solver
 - Good interpersonal, networking and teamwork skills
 - Excellent organizational and time management skills
 - Critical thinking and proactive work style
 - Willingness to travel (10-15%)
 
We offer
- Very varied area of responsibility in a complex environment
 - Career opportunities in an international pharmaceutical company
 - Training opportunities and personal development within the company
 - Annual gross salary starting from EUR 65.000,-. The willingness to overpayment, according to skills and experience, is given
 
Apply
Offre archivée le 08/07/2024
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