Job Description
The Quality Assurance Documentation Coordinator is responsible for overseeing the management of key quality systems, preparing and approving site documentation, tracking schedules, escalating issues, and administering training.
Key responsibilities include coordinating records retention, managing control of all records through the Records Management process, and providing document management metrics and training reports as needed.
Requirements include at least 2 years of experience in a similar position with skills in documentation quality, GMP pharmaceuticals, and analytical records.
The ideal candidate will have excellent communication skills and be able to work effectively in a team environment.
Additionally, they will have strong problem-solving skills, attention to detail, and the ability to prioritize tasks efficiently.
This role offers an opportunity to develop expertise in documentation management and contribute to the success of the organization.