- 経験
- 2～4歳
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 12時間前
- 作業モード
- 在任中
- 教育
- B.Pharm/MSC/M.Pharm
- 再開する
- 応募必須
勤務地
仕事内容
Job Overview
The role requires conducting analyses on stability and finished product samples, preparing detailed reports following ALCOA standards, and other miscellaneous samples with their respective documentation.
Key Responsibilities
- Carry out analysis of stability and finished goods samples, documenting results precisely in line with the ALCOA procedure.
- Manage the operation and upkeep of laboratory instruments including Dissolution Test apparatus, UV spectrophotometer, analytical balances, pH meters, and sonicators.
- Ensure compliance with data integrity policies, Good Documentation Practices (GDP), and maintain their ongoing effectiveness.
- Oversee the maintenance and monitoring of the stability chambers and maintain the tracker system.
- Manage the charging and withdrawal of stability samples strictly according to approved protocols.
Qualifications and Experience
- Educational background in B.Pharm, MSc, or M.Pharm.
- Possess between 2 to 4 years of relevant experience in the pharmaceutical industry.