Job Description
- Prepare QA and QC documents in accordance with quality management standards and external regulations
- Assist in internal audits and batch manufacturing and packing records checks in accordance with cGMP standards on production batches to ensure product quality
- Maintain quality manual and SOPs for quality procedures, and assisted in creating new procedures and SOPs where required
- Maintain quality records such as batch manufacturing and packing records, monitoring, testing, and validation records
- Assist in all quality audits and inspections conducted by local and foreign health authorities
- Any other tasks as assigned
Requirements
- ITE/NITEC in Chemical Process or Diploma in Pharmaceutical Science with 1 year experience
- Fresh graduates are welcome.
- Computer-literate (i.e., Word, Excel, PowerPoint)
- Good communication and interpersonal skills
- Candidates with pharmaceutical experience have an added advantage
- Able to start work within short notice
