23.04.24 | Vollzeit | Mainz | SCHOTT AG130 years of outstanding development, materials and technology expertise we offer a broad portfolio of high-quality products and intelligent solutions. SCHOTT is an innovative enabler for many industries, including the home appliance, pharmaceutical, electronics, optics, life sciences, automotive
Später ansehen24.04.24 | Vollzeit | Mainz | SCHOTT AGSCHOTT is a leading international technology group in the areas of specialty glass and glass-ceramics. With more than 130 years of outstanding development, materials and technology expertise we offer a broad portfolio of high-quality products and intelligent solutions. SCHOTT is an innovative
Später ansehen24.04.24 | Vollzeit | Mainz | SCHOTT AGAnd identification of innovative product ideas and business areas - Proven track record of successful cooperation in international projects as a member of a cross-functional teams, ideally project management experience - Fluent business English (written and spoken), knowledge of other languages and willingness
Später ansehen25.04.24 | Vollzeit | Mainz | BioNTech SEAdministration At least 10+ years of professional experience within the pharmaceutical or biotech industries within quality, production, supply chain, project management or other
Später ansehen22.04.24 | Vollzeit | Mainz | SCHOTT Pharma AG & Co. KGaAAs well as the consolidation of systems and harmonization of master data - Conduct ad-hoc analysis of financial data and prepare information for management and supervisory bodies - Work closely with other controlling and finance departments of SCHOTT Pharma, as well as SCHOTT Group Your Profile - You
Später ansehen18.04.24 | Vollzeit, Teilzeit | Ingelheim am Rhein | Boehringer IngelheimSich alles um die Herstellung pharmazeutischer Wirkstoffe und deren Vorstufen, die die Kernbestandteile der Arzneimittel von Boehringer Ingelheim ausmachen. Innerhalb der Chemical Site Ingelheim verantwortet der Bereich Production Excellence and Compliance die chemischen Herstellprozesse unserer Wirkstoffe sowie deren
Später ansehen16.04.24 | Vollzeit | Ingelheim am Rhein | Boehringer IngelheimAnd dynamic CMC Technical Development Leader (TDL) to spearhead technical development projects, create robust products, and lead cross-functional teams. If you have a strong background in science, a track record in pharmaceutical drug development, and the ability to lead without authority, we invite you
Später ansehen20.04.24 | Vollzeit | Mainz | SCHOTT Pharma AG & Co. KGaAAt our fingertips. - Evaluate and implement software tools, working hand in hand with IT to streamline regulatory processes. - Play a pivotal role in harmonizing the quality management system in the regulatory realm. Your Profile - A university degree in Science (biotechnology, pharmacy, pharmaceutical
Später ansehen20.04.24 | Vollzeit | Trier | JT International Germany GmbHScientific and Regulatory Affairs department (SRA) in Trier, we are looking for a Material Assessment Manager (m/f/d) in permanent employment. Your job mission You will contribute to a robust and defensible portfolio of JTG (Japan Tobacco Group) products and be part of a dynamic, global team that values
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