Valeant Pharmaceuticals

  • Sr Laboratory Quality Compliance Specialist

    Location US-NY-Rochester
    Job ID
    10837
    Category
    Quality
    Pos. Type
    Full Time
  • Overview

    This role provides oversight and review of laboratory systems and data.  Responsible for ensuring the data integrity of laboratory information systems, processes, and data.

    Responsibilities

    • Perform routine surveillance/review of data generation process including paper and electronic data
    • Participate in the development of continuous improvement efforts for compliance in both chemistry and microbiology laboratories
    • Remain current on the regulatory landscape related to laboratory compliance requirements and suggest improvements
    • Lead training efforts in data integrity practices on a local and/or regional basis
    • Participate in internal audits, self-inspection reviews, and audits of suppliers as it relates to lab compliance.
    • Maintain laboratory metrics
    • Lead Laboratory Operational Excellence activities

    Scope of Position:

    This position will have responsibility for laboratories with GMP activities within the R&D process related to lens care solutions and pharmaceutical product development. 

    Qualifications

    B.S. degree in science field, plus 5 years' experience in GMP laboratory. Previous experience in quality preferred.

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