Title: Pharmaceutical Quality Assurance Specialist
Location: Lansdale, PA
Duration: 12 months
Qualifications
The primary role will be to support the Quality Management Systems teams with various tasks including, but not limited to documentation and project support activities. The role requires interaction with learning management systems; MyLearning and Quality Docs.
Required Education & Skills:
Preferred Education & Skills:
Responsibilities
Primary Responsibilities include.
Key collaborator working closely with site personnel and Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS by assisting with project-specific tasks, including but not limited to, project support, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.
Specific tasks may include:
NOTE : The Clinical Supply Quality Management System (QMS) team is part of the larger Global Development Quality (GDQ) organization within Quality Assurance and is responsible for the design, implementation, and long-term maintenance of a new QMS, including Quality Standards and Global Procedures, for all sites performing Clinical Supply functions within the client’s Global network
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