Senior Expert Science & Technology (Process Analytical Sciences)(m/w/x)

Management

Vollzeit

ab 65.606 / Jahr

Schaftenau

Nejo KI-Zusammenfassung

In this role, you will lead analytical projects and develop strategies for drug substance and product processes. Your expertise will drive collaboration with teams and partners, ensuring efficient project execution and compliance with regulatory standards.

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Anforderungen

•University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
•At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
•Advanced knowledge within the area of Analytical Development
•Expertise in Biologics DS and DP process development applying QbD principles
•Solid project management skills
•Excellent collaboration skills
•Proficiency in oral and written English; German is beneficial
•Strong proficiency in digital technologies

Bachelor-Abschluss

Berufserfahrung

3 Jahre

Deine Aufgaben

•Lead analytical project activities as a matrix leader
•Establish physicochemical analytical strategies based on Quality by Design principles
•Interpret and contextualize analytical results
•Apply data and digital solutions to enhance efficiency
•Lead or support root cause investigations and issue resolution
•Monitor project progress and represent analytical aspects in meetings
•Oversee in-house and outsourced analytical work to meet timelines
•Author and review scientific reports for regulatory submissions
•Act as an analytical expert during audits and inspections
•Manage multiple priorities and proactively communicate challenges
•Contribute to budget and resource planning while maintaining cost awareness
•Build strong relationships with internal teams and external partners
•Promote knowledge sharing and present results internally
•Contribute to publications, presentations, and patents
•Evaluate new analytical technologies and develop innovative methods
•Ensure alignment with scientific standards and contribute to digitalization efforts
•Respond to analytical queries during audits and regulatory reviews
•Ensure data integrity in CMC modules

Sprachen

Englisch – verhandlungssicher

Deutsch – Grundkenntnisse

Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Novartis Pharmaceutical Manufacturing GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.

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