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document control in Chicago

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    1. Director of Med Affairs Clinical Operations Efficiency & Communication

      Shall: *** Collaborated to facilitate study designs, analytics, data interpretation, clinical development programs, and hypotheses generation development and validation. *** Support in Phase III-IV clinical trials in Oncology and Immunology. *** Reviewed Global ...

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      No Telecommute

    2. Technical Writer

      Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career ...

    3. Distribution Supervsior

      Our Company We are a rapidly growing pharmaceutical manufacturer, with core competencies in the sterile injectable and ophthalmic sectors, and with many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer ...

    4. Manager, Formulation Research and Development

      Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career ...

    5. Clinical Research Associate - Midwest Region - Home-Based

      PSI CRO AG - Home-based - Midwest Region PSI is expanding rapidly in the US and seeking highly motivated CRAs. At PSI, we believe employees are our greatest assets. Responsibilities: Project activities and monitoring functions associated for Phase I-IV clinical research ...

    6. Quality Systems Specialist

        Description:   Quality Systems Specialist with experience establishing and maintaining documents within the quality system.  Skilled in document change control and able to smoothly facilitate change requests throughout their lifecycle -- from initiation through approval ...