Kitchen manager in állások, munkák egészségügy, gyógyszeripar területen

• Plan and perform drug discovery contract research studies
• Executing bioassays
• Data evaluation and interpretation
• Prepare study reports in English
• Summarize data, analyze results and formulate conclusion
• Work with other project team members and communicate results with the team

• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Receipt / Download / Accept cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

• Literature reviews as requested by client epidemiologists using the best practice methodologies
• Literature search and preparation of Literature review report for Pharmacoepidemiology
• Perform peer Scientific & Technical Review

• QC of ICSR related activities to ensure compliance to Customer and regulatory agency requirements.
• Case intake activity for ICSRs related performance during the work.
• Ensure the Quality and TAT targets are defined and met.

• 40 hours per week
• Normal business hours
• Office attendance: Once a week
• Tracking different regulatory submissions in the corporate regulatory database – update database with specific documents and/or information
• Running daily queries, providing reports to client stakeholders

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

• Location: Budapest, Hungary, 9th District, Mill Park office building
• Job Type: Full-time
• Normal office hours
• Hybrid work mode

• Location: Budapest, Hungary – 9th District, Mill Park office building
• Job Type: Full-time
• Contract: Maternity cover (until the incumbent returns)
• Office Presence: Required once per week

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

Organize and coordinate internal and external learning and training activities - from planning and scheduling to attendance management and training evaluation. ...

• Coordinate laboratory projects and daily laboratory activities
• Schedule and monitor laboratory tasks and deadlines
• Prepare, manage and maintain laboratory documentation
• Handle technical documentation and certificates
• Prepare regular reports and summaries related to laboratory activities

Investigating and understanding the manufacturing processes and used raw materials, as well as troubleshooting issues and improving process efficiency....

• Organizational and administrative management of Kecskemét plasma center in cooperation with the Lead Physician and the Quality Management Representative
• Defining and implementing an expedient center strategy
• Leading a team of nurses and physicians – support, develop, motivate, provide regular training

• Develop, modify, and maintain quality evaluation and control systems for materials, in-process parts, and finished products.
• Translate product requirements/specifications into test plans, methods, and fixtures to ensure product reliability.

Analyze customer requirements and support solution design and architecture of trial sponsors or contract research organizations (CRO) in Vault Clinical (e.g., eTMF, CTMS, SSU, Payments, etc.)...

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• Mit Ihrem Gespür für individuelle Bedürfnisse beraten Sie unsere Gäste zu Spa-Dienstleistungen und hochwertigen Pflegeprodukten.

• Erfolgreich abgeschlossene Ausbildung sowie praktische Erfahrung in den Bereichen Teilkörper- und Ganzkörpermassagen, von Vorteil Erfahrung im Auftragen von Peelings und Machen von Packungen
• Freude am Umgang mit anspruchsvollen, nationalen und internationalen Gästen