Precision Life Sciences is seeking a contract, Quality Assurance Documentation Specialist for our client in the life science / biotechnology industry. This position will be responsible for partnering with cross-functional team members to ensure compliance with GxP documentation. The QA Documentation Specialist must have experience in authoring, editing, reviewing, evaluating, and maintaining documents in a GxP environment. This position will implement processes and systems associated with document management to align with quality and business objectives.
This role has responsibility for:
Must thrive working in a fast-paced, innovative environment while remaining flexible, proactive, resourceful, and efficient. The individual will need to effectively partner with various stakeholders throughout the organization. The QA Document Specialist requires excellent organizational skills, attention to detail, diligence, and flexibility as well as the ability to prioritize responsibilities.