Cad administrator Jobs in Weilrod
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Cad administrator • weilrod
Manager Process Control Strategies (m / w / d)
FRESENIUS_KABIOberurselCNC-Fachkraft Schwerpunkt Fräsen (m / w / d)
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Rolls-RoyceOberurselSAP-Basis-Administrator (m / w / d) •
ALH GruppeOberurselManufacturing Support Lead _CMM_ Oberursel, Germany
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Bader & Kara Zeitarbeit GmbHOberursel (Taunus)- Gesponsert
Application Administrator •
Seibert Group GmbHIdstein (Hochschulstadt), DEIT-Administrator Linux (m / w / d)
HaysHessenTechnischer Systemplaner – Versorgungs- und Ausrüstungstechnik (VAT) (m / w / d)
Teamplan Ingenieure GmbH von MINTbund.deOberursel, Hessen, DE- Gesponsert
Ausbildung zum Technischen Produktdesigner im Maschinen- und Anlagenbau (m / w / d)
Verfahrenstechnik Schweitzer GmbHNeu-Anspach, Hessen, Germany- Gesponsert
Bauingenieur als Tragwerksplaner / Statiker im Hochbau (m / w / d) - Projektmanagement, IT
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Jago ConsultantsHessen, GBCAD-Konstrukteur (m / w / d) Entwicklung Ballistik
ISG International Service GroupHesse- Gesponsert
Application Administrator •
Seibert Group GmbH - KarriereIdstein, Hessen, DE- Gesponsert
Technical Consultant ServiceNow (m / w / d) Teilzeit möglich
operational services GmbH & Co. KGverschiedene Standorte, Hessen, GermanyKonstrukteur / Produktdesigner / Technischer Zeichner (m / w / d)
PERMACON GmbH FrankfurtOberursel, DeutschlandMitarbeiter - Dokumentation (m / w / d)
innomatec Leak Test SolutionsIdsteinManager Process Control Strategies (m / w / d)
FRESENIUS_KABIOberurselYour assignments
Development, improvement, and implementation of technical Standards for process control strategies for GMP regulated sterile production environments,
Support of production sites in establishing risk-based control strategies for manufacturing and support processes
Compliance assessments of process control strategies within company’s production network, assessment of GMP compliance of equipment, utilities and facilities
Technical support and internal consulting in engineering projects for new and renovated equipment, utilities, and facilities
Analysis of manufacturing processes regarding process improvements and support in implementing process improvements and controls
Support in implementing modern, digital quality concepts in production environments
Preparation of and response to authority inspections
Design and evaluation of qualification and validation strategies and support in qualification / validation projects
Internal consulting regarding technical GMP requirements
Review and check of technical documentation
Your profile
University degree in relevant engineering disciplines or equivalent
Min. 3 - 5 years of vocational experience in sterile manufacturing environments or in engineering and design of sterile manufacturing processes / facilities
Relevant vocational experience on international level, work within or leadership of international teams and intercultural skills
Excellent knowledge of technical norms / standards, international GMP-requirements and guidelines (ISPE, PDA etc.)
Experience in sterile pharmaceutical production process and the respective regulatory requirements
Experience in applying quality tools and methods
Experience in qualification of equipment, utilities and facilities and process validation
Knowledge of statistical tools
Willingness to travel (internationally)
Fluent in English, further language skills are advantageous
IT knowledge : MS Office, Visio, technical applications, CAD, Minitab etc.