Administrator: QA Processes
- Gauteng
- Permanent
- Full-time
- Process documents
- Capturing, Logging, and tracking Deviations on the Deviation log
- Filing of Deviations as required (electronic or paper based)
- Logging, tracking, and assisting with closure of SCAR Reports.
- Capturing, Logging, and tracking Risk Assessment Register
- Compilation of monthly reports and trends for deviations and non-conformances
- Assist in monitoring and adherence to all in-house quality assurance standards.
- Assisting in follow-ups for to ensure Deviations and Hold notices are closed timeously
- Assisting in follow-ups for to ensure SCARS are closed timeously
- Continuous improvement of storage of records for Deviations
- Ensuring release department receives required deviations
- Matric Certificate (minimum requirement)
- Science Degree
- Competent in MS office and Excel
- Minimum 3 years of QA experience in pharmaceutical company is required
- Computer literate
- Interpersonal skills and self-driven
- Good oral and written communication skills
- Ability to work under pressure
- Must be able to work in a team and independently
- Proactive
- Effective communication skills
- Technical Skills
- Team Player
- Problem solving
- Attention to detail