Documentation Specialist (GMP)
Novartis
This listing was originally posted on Novartis's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
Job Description Summary
Sie haben ein Auge fürs Detail, arbeiten gerne strukturiert und möchten die Produktionsdokumentation in einem GMP-regulierten Umfeld unterstützen? Dann sind Sie bei uns genau richtig.
Job Description
Hauptverantwortlichkeiten:
Mindestanforderungen:
Ausbildung im administrativen Bereich
Erfahrungen in einem Produktionsbetrieb sind von Vorteil
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
General Hse Knowledge , gmp knowledgeExplore related positions you might be interested in
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PHARMACEUTICAL
Small Molecules, Vaccines, Biologics / Diagnostics
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