Takeda
Product Quality Expert(m/w/x)
Vollzeit
Berufserfahren
Keine Angabe
Neuenburg
TA
Takeda11 Tage
Product Quality Expert(m/w/x)
Vollzeit
Berufserfahren
Keine Angabe
Neuenburg
Nejo KI-Zusammenfassung
In this role, you will ensure product quality by preparing reviews, managing regulatory documentation, and participating in audits. You will collaborate with experts to streamline processes and support product launches, making a significant impact on quality assurance.
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Anforderungen
- •University degree in technical/scientific discipline or equivalent
- •At least 3-5 years of experience with manufacturing in biotechnology and/or pharmaceutical industry
- •Experience in writing and/or reviewing eCTD licenses
- •Experience with regulatory affairs framework (CMC)
- •Good knowledge of FDA, EMA, ICH regulations and quality system standards
- •Experience as a change owner or project leader
- •Knowledgeable in GMP inspections and management of regulatory/quality standards
- •Fluency in English and French
- •Knowledge/Experience with quality tools such as Trackwise 8, Veeva, eCTD viewer
- •Ability to work in a controlled environment requiring special gowning and protective clothing
- •Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails in manufacturing environment
- •Ability to work around chemicals requiring respiratory protection
Bachelor-Abschluss
Berufserfahrung
3–5 Jahre
Deine Aufgaben
- •Prepare Product Quality Reviews (PQR) annually for products manufactured at the Neuchâtel facility
- •Review global release specifications and implement updated versions for Neuchâtel products
- •Participate in GMP tours to ensure inspection readiness
- •Manage and prepare documentation for regulatory submissions and major change projects
- •Prepare and review documentation for change controls and audit observations
- •Support and write responses to regulatory agency questions, collaborating with Subject Matter Experts as needed
- •Assist in the preparation of inspections and required documents
- •Participate in audits and inspections as required
- •Help define strategies for responses to health authority questions as part of the quality matrix team
- •Update inspection records in TrackWise when necessary
- •Propose improvement initiatives to streamline tasks
- •Assist in the preparation and review of quality documentation
- •Participate in Quality Council meetings as necessary
- •Support coordination of site Key Performance Indicators (KPIs)
- •Participate in project teams based on expertise and project focus
- •Engage in product launch activities
- •Identify opportunities to improve quality processes
- •Collaborate with global Quality Product Leads and Regulatory Affairs partners
Tools & Technologien
Trackwise 8VeevaeCTD viewer
Sprachen
Englisch – verhandlungssicher
Französisch – verhandlungssicher
Deine Vorteile
Mehr Urlaubstage
- •28 days of paid time off
Gesundheits- & Fitnessangebote
- •Sport/Fitness abonnement contribution
- •Medical annual check-ups starting at age 50
- •Financial support for preventive healthcare
Gratis oder Vergünstigte Mahlzeiten
- •On-site cafeteria
Großzügige Elternzeit
- •Paid leave for maternity
- •Paid leave for paternity
- •Paid leave for adoption
Kinderbetreuung
- •Dedicated spaces for nursing mothers
Weiterbildungsangebote
- •Access to a Learning Catalog
- •Language courses
Karriere- und Weiterentwicklung
- •Opportunities for internal mobility
Workation & Sabbatical
- •Opportunities for international mobility
Öffi Tickets
- •Contributions for public transport
Firmenfahrrad
- •Incentives for e-biking
Parkplatz & Pendelvorteile
- •On-site charging stations for electric vehicles
Team Events & Ausflüge
- •Regular on-site gardening activities
Mentale Gesundheitsförderung
- •Regular on-site massages
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Takeda 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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