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document control in Chicago

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    1. Quality Control Specialist

      Description of Work: Accountable for directly interfacing with suppliers analyzing and confirming data on products & materials Understanding the regulatory convenience kit guidelines applicable for medical devices & drugs, utilizing this data to apply to position ...

    2. 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 ...

    3. Validation Manager

      JOB SUMMARY: Provides management oversight for the Validation and Quality Engineering efforts at the facility. Responsible for administration of the company's Validation Department and implementation and Validation and Quality Engineering policy.  Work towards continuously ...

    4. Regulatory Affairs Associate

      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. Regulatory Affairs - Animal Health

      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 ...

    6. Document Control/Technical Writer

      Hello, My name is Chrys and I represent The Fountain Group. We are a national staffing firm and are currently seeking an Technical Writer for a prominent client of ours. This position is located in North Chicago, IL Details for the position details are as follows: Job ...

    7. Senior Biostatistician

        The Senior Biostatistician capably applies knowledge of statistics to independently provide statistical consulting, assist with study design and protocol development, performs statistical analysis of clinical trials. Review project related documents. Prepares statistical ...