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Quality Systems Specialist II

Job ID: 219879

Location: Framingham, Massachusetts , US, 01701

Summary:

Supports compliance, maintenance and improvement of the global quality management system. Assists in all quality system activities. Supports development and implementation of Quality Management System (QMS) and supporting infrastructure/tools in compliance with FDA Quality System Regulation (QSR) regulations, International Standards Organization (ISO) regulations, and internal corporate requirements.

Project Details:

  • Actively participate in audit preparation efforts by supporting planning, gap analysis, and mitigation implementation activities required to comply with new regulations and standards.
  • Responsible for supporting generation of QMS documentation using Electronic Document Management System (EDMS).
  • Support coordination of document and record retention program for the site in alignment with the internal corporate requirements.
  • Write and revise Quality Systems procedures, perform gap assessments and assist in driving compliance.
  • Exposure to internal, external, laboratory, supplier auditing programs as appropriate.
  • Maintain processes/procedures to ensure compliance to internal and external requirements.
  • Provide compliance support for Quality Assurance, Regulatory Affairs, R&D, and Operations to assure regulatory compliance and appropriate business planning.

Job Experience:

  • Understanding of manufacturing procedures and GMP requirements is a plus
  • Experience in Change Management, Inspection and CAPA Management is an added advantage
  • A proven ability to work creatively and analytically in a problem-solving and process-oriented environment
  • Expected to operate independently, accountable to proactively fulfill tasks and achieve results within assigned timelines
  • A proven ability to work in a collaborative, team-based environment dependent upon effective teamwork to achieve goals and company objectives
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