We are looking for a motivated, self-driven Qulaity Assurance Analyst with LabWare LIMS expereince. This person will maintain ongoing LIMS configuration in support of business process change of the LabWare LIMS application.
Responsibilities:
* Creat and modify objects in the LabWare LIMS database * Design and configure master data objects in support of procedures and conformance standards * Develop and execute test scripts for master data objects in a cGMP manner * Work as a system analyst supportuing the LabWare LIMS system.
Qualifications & Requirements
Requirements:
* Minimum requirements include a Bachelor's degree in a scientific discipline and 1-3 years pharmaceutical or biopharmaceutical industry experience. * Qualified candidates must have configuration/development experience with applications in a regulated laboratory environment. * Must have knowledge of industry application configuration and usage. * Experience with implementation, integration, validation, and maintenance of LabWare LIMS in a regulated environment is required. * Ability to communicate effectively with end users and team members both in writing and verbally. * Requires effective organization skills, attention to detail and ability to execute on defined procedures and processes.
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