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[Cassiopeia-generic] grand total


From: Matty Torres
Subject: [Cassiopeia-generic] grand total
Date: Sat, 14 Oct 2006 03:44:35 +0300
User-agent: Thunderbird 1.5.0.7 (Windows/20060909)


Writing master cleaning validation plans. Requirements: Strong experience in an applications development environment programming with SAS software. Generation of item code, Bar Code for artwork preparations. CW agent detection and analysis of data. Plan and document testing tasks.
Coordinate with customers re: validation protocols.
Requirements: In depth knowledge of data visualization for statistical and analytical applications.
Apply innovative techniques in designing and unit testing of the product. net and other solutions.
Interact directly with developers to test software, resolve bugs, and incorporate quality in the SAS product during the development and QA cycle.
Research and implement appropriate statistical and machine learning methods. In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting.
Nature of products: monoclonal antibodies.
CW agent detection and analysis of data. He should be able to give patent evaluations to support the present on going projects.
Understanding of mechanism of action of drugs, cell signaling, gene _expression_ and regulatory pathways is desirable.
Apply innovative techniques in designing and unit testing of the product. Ability to research new and innovative techniques for effective visualization of data Excellent knowledge of Java, Java-Swing, JSP.
Design, develop, execute, verify, and analyze test programs and procedures.
Generation of item code, Bar Code for artwork preparations.
Degree in Chemistry or related discipline. Degree in Chemistry or related discipline. Ability to research new and innovative techniques for effective visualization of data Excellent knowledge of Java, Java-Swing, JSP.
Work with Business Analysts, gather functional requirements, and ensure that supported data model conforms to these requirements as well as modeling standards. Writing batch records. Anticipate time needed to complete projects and assist in modular product scheduling. Adhere to the regulatory bodies - and coordinate between US, EU and UK. Hands on experience in physiological and pharmacological assessments and expertise in surgical skills in small animals is mandatory . Provide support and maintain released data models and existing ones. Experience with gas and vapour detection, environmental testing. Determine specific needs of end users; design and implement software, etc. Appropriately documents and validates statistical programs.
Report to the Regulatory Affairs Director.


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