Compliance Specialist

  • Contract

Job Description

  • Utilize root cause analysis techniques during deviation investigational process
  • Work cross functionally, to develop and implement continuous process improvements
  • Support production needs and continuous improvement including change control, deviation writing / review, CAPA implementation, and operational optimization.
  • Collaboration with Technical Writers to write, review, revise and prepare manufacturing documents (BPR, SOP, SWI, etc) in accordance with cGMP and regulatory guidelines.
  • Communicate across multiple groups and levels to obtain consensus in order to facilitate deviation closure
  • Manage multiple priorities either independently or part of a team in order to meet key deadlines and communicate issues and progress across all levels of organization

Additional Information

All your information will be kept confidential according to EEO guidelines.