• PSG Global Solutions
  • Jersey City , NJ
  • Pharmaceutical/Biotechnology
  • Full-Time
  • 10 Bayside Terrace

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The Opportunity

We're looking for a Documentation Specialist III, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey.

Work with the functional groups in North America Business Operations to create/revise Quality Documents.Support the operation and maintenance of the Quality Document Operations.Engage with stakeholders to migrate and manage Quality Documents across Business units. Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.Engage with stakeholders to align local Quality Documents with Global policies and guidelines.Manage the user access requests for the quality document management system rights.Maintain a constant state of sustainable compliance and inspection readiness for all activities related to the Training and Quality Document Functions including, but not limited to, lifecycle management of Quality Documents, accuracy of training curricula, and CV/JDs for areas of scope. Generate reports from the Learning Management System and provide compliance reports as needed during audits, monitoring and routine oversight activities. Manage the shared Outlook mailbox; interfaces with learners/stakeholder and follows requests through to completion.Manage the training Notification & Escalation Process. Manage the Personnel Change Workflow by analyzing reports to identify new hire & terminations and proceeding with curricula updates.
Associated topics: advertising, advertising promoting, brand ambassador, brand marketing, business, direct, market, marketing, product marketing, project manager

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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