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  • 498 Washington St, Coventry, RI 02816, USA
    Req #99
    Monday, November 15, 2021
    Job Summary: The Manager, Portfolio and Project Management will be responsible for providing Project Management support to Rhodes Pharmaceutical’s internal and external development programs. The Project Manager will support the generation and execution of project plans in collaboration with Business Development, Product Development, Operations dept., etc. for multiple development, & in-licensed projects within multiple therapeut ... More
  • Rhodes Technologies, 498 Washington Street, Coventry, RI, USA
    Req #78
    Friday, July 16, 2021
    Job Summary:   With close supervision, this position will assist analytical method development, validation, and transfer, stability testing and activities to support regulatory filing and clinical studies in compliance with all applicable guidelines. This position will conduct routine sample analysis for prototype formulation development and some advanced laboratory procedures utilizing appropriate instrumentation. This position may author laboratory Standard Operating Procedures (SOPs), metho ... More
  • Rhodes Technologies, 498 Washington Street, Coventry, RI, USA
    Req #77
    Friday, July 16, 2021
    Job Summary:   This position will act as analytical lead and support drug development through analytical method development, validation, transfer, stability testing and activities to support formulation development and clinical studies in compliance with all applicable guidelines with minimum supervision. This role may independently identify/observe problems and recommend experimental strategies and solutions. This position will develop and author laboratory Standard Operating Procedures (SOP ... More
  • Rhodes Technologies, 498 Washington Street, Coventry, RI, USA
    Req #72
    Tuesday, June 22, 2021
    Job Summary   The Quality Assurance (QA) Specialist III is a position that supports several Quality Systems. The position conducts technical quality compliance related activities in accordance with GxP regulations and internal SOP’s. Primary responsibilities include coordinating documentation in support of global submissions, routine SOP revisions, Annual Product Reviews, Batch Record Issuance, and EDMS (MyQUMAS) Administration. Primary Responsibilities Ensures that documentation is maintaine ... More