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Fresenius Kabi AustriaOrt
GrazSenior Manager Drug Product Process Development and Manufacturing (m/f/d), Graz
Unbefristeter Arbeitsvertrag
Pharmaindustrie
Gesundheit
Medizintechnik
Gesundheit
Medizintechnik
Ingenieur
Techniker
Techniker
Die Stellenanzeige wurde am 08/07/2024 archiviert.
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
Die Stellenanzeige wurde am 08/07/2024 archiviert.