職位描述
Responsibilities:
- Finish the routine analytical work accurately and timely
- Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status
- Double-check the BAR
- Responsible for the management of chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory
- Responsible for the handling and disposal of lab wasted articles/expire reagent/toxic substances
- Report any deviation timely and assist in investigation
- Stability study and test
- Equipment & Column routine maintenance
- Issue and revise specification, test method and batch analysis record of starting materials and finished products, and purchasing specification, test method for PQ, CQ etc.
- Prepare specification for application (draft) and specification explanation
- Check specification and test method for import products together with Regulatory department
- Technology transfer and method validation/verification
- Fill in related documentation such as BAR, other logbook etc., timely to ensure the accuracy of content as per requirement of SOPs
- Take part in actively in correction to the observations found in self-inspection
- Assist and support the group leader in leading the associated teams when required
- SHE responsibilities
Requirements:
- University or above
- Basic GMP, GLP knowledge; Experience in QC
- More than 3-4 years working experience in pharmaceutical company or related industry
- Good English command
- Good computer skill
- Good teamwork spirit
- Sense of responsibility and work actively
阿斯利康聲明：
1. 本公司招聘工作均由本公司人力資源部主持，在面試流程中，無需候選人提交除簡歷之外的其他個人信息，無需繳納任何保證金或費用，無需付費參加任何培訓課程。請求職者謹防詐騙信息。
2. 本公司所有招聘均通過直接面談、電話溝通、EMAIL（以@astrazeneca.com為后綴）方式進行。
3. 對于未經本公司允許發出相關招聘信息的行為，阿斯利康公司保留追究其法律責任的權利。
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