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Once commissioning of the facility is complete, the associate quality control will transition to performing routine sampling and testing in the GMP Manufacturing facility in support of the Microbiology and Environmental Monitoring group.
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He or she will work to elicit additional protocol requirements from the clinical team, then partner with the IRT vendor to ensure the IRT system is programmed according to the protocol, test scripts are complete and accurate, and execute User Acceptance Testing (UAT) in order to successfully deploy the system into production.
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Located in our Cambridge, MA office, the PD Associate Scientist will work to provide testing support for commercial process development and process characterization studies for clinical candidate molecules in the pivotal stage of development.
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Min 2 years' experience performing analytical testing. Job Title: Sr Associate. Master's degree in Analytical Chemistry, Physical or Pharmaceutical or Life Sciences or Engineering related discipline.
$25 - $29 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Perform testing (UAT & Regression Testing) as required for any coding or configuration changes made to the site or supporting ecosystem, document test execution results (JIRA & Client ALM) and log bugs.
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Consult and ensure on time delivery of user acceptance testing of IRT systems consistent with Client SOPs and procedures. Job Description: IRT Business Associate. Lead successful execution and on time delivery of Interactive Response Technology (IRT) and support integrations with other clinical systems (e.g., Depots, Central Lab, and EDC), such that the resultant IRTs are fit-for-purpose as defined by protocol and study operational parameters with special emphasis on adherence to Client standards and quality principles.
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8 Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing. Requirements: Minimum BS degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and.
$28 - $32 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Under general supervision, this position will perform routine procedures and testing in support of the HPLC and CE (Capillary Electrophoresis) group. - Routine analytical testing. Job Title: Associate Quality Control.
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The individual will also participate in projects related to the development of microfluidics platforms to support toxicity testing for our drug discovery program. Genentech has an open Scientific Researcher position in the Investigative Toxicology group within the department of Safety Assessment located in our South San Francisco campus.
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Maintains program and facility standards to ensure compliance of research facilities, husbandry practices, and in vivo testing procedures to all applicable regulations. Maintains program and facility standards to ensure compliance of research facilities, husbandry practices, and in vivo testing procedures to all applicable regulations.
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Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements. This position works a rotating shift schedule, Week 1: Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday, Thursday, ~12 hours per day 6:45 AM – 7:00 PM.
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In this individual contributor, lab-based role, the Associate Scientist will work in a collaborative environment to perform analytics testing to support multiple Client programs. Execution of routine analytical testing including qPCR, ddPCR, ELISA, molecular biology, and cell-based assays to test in-process vector samples.
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Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents.
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