Report to the Regulatory Affairs Director.
Nature of products: monoclonal antibodies. Responsibilities will include, but not be limited to developing and implementing lean methodologies, incorporating methods of process improvement and providing support for the quality system.
You will work within specified timeframes on multiple projects in a commercial setting. Interest in quality and validation.
CW agent detection and analysis of data.
Adhere to the regulatory bodies - and coordinate between US, EU and UK.
Responsibilities will include, but not be limited to developing and implementing lean methodologies, incorporating methods of process improvement and providing support for the quality system. Prepare summary reports of information.
Your duties will include the design, implementation, and testing of key software components of the Verseon proprietary drug discovery platform.
Anticipate time needed to complete projects and assist in modular product scheduling.
Ability to research new and innovative techniques for effective visualization of data Excellent knowledge of Java, Java-Swing, JSP. In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting. Knowledge and experience of computer programming, databases, process control.
You will co-ordinate all communications with the technical team, Quality Assurance and the Sponsor.
Excellent written and verbal communication skills are required. Comply with GCP procedures, EU regulatory affairs.
Nature of products: monoclonal antibodies. Interest in quality and validation.
Requirements: In depth knowledge of data visualization for statistical and analytical applications. Experience with gas and vapour detection, environmental testing. Appropriately documents and validates statistical programs.
Experience in writing and executing validation documentation. Knowledge and experience of computer programming, databases, process control.
Excellent written and verbal communication skills are required.
Redesign graphics in .
in synthetic organic or medicinal chemistry, with a track record showing appropriate and relevant proficiencies.
Interest in quality and validation.
Requirements: In depth knowledge of data visualization for statistical and analytical applications.
Report to the Regulatory Affairs Director.
Report to the Regulatory Affairs Director.
CW agent detection and analysis of data.
Liaise with physicians and attend meetings. BW agent detection and analysis of data. Writing batch records. CW agent detection and analysis of data.
Police the protocols within manufacturing.