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:
Bachelor's Degree in an appropriate scientific or business field of study
Minimum of five (5) years' experience in the Pharmaceutical or equivalent industry
Strong technical knowledge, skills, and experience in project and documentation management
Preferred Education & Skills:
Responsibilities:
Primary Responsibilities include.
Specific tasks may include:
Perform documentation review and technical editing to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply network
NOTE: The Clinical Supply Quality Management System (QMS) team is part of the larger Global Development Quality (GDQ) organization within Client Research Laboratory (MRL) 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 Global network.
Quality Reviewer • Rahway, New Jersey, United States
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