QA-Technical Analyst
สถานที่ทำงาน
พระนครศรีอยุธยา - พระนครศรีอยุธยา
สายงาน
เภสัชกรรม
เงินเดือน
ไม่ระบุ
ความสามารถด้านภาษา
ชาวต่างชาติสามารถสมัครได้
ไม่ได้
ลักษณะงาน
หน้าที่และความรับผิดชอบ
This position is assigned for handling of control specification and all procedure of QC part according to the established product specifications and procedures. Also keep compliance to ensure that the documents part for registration are correctly.
Responsibility:
- Verify finished product & shelf life specifications for new product and update dossier for current product.
- Provide product specifications, analytical method, equipment or provide comparison of specification and test method as client request.
- Prepare official finished product specification and analytical method.
- Prepare product control record/ COA.
- Prepare the dossier for regulatory submission and responsible for the regulatory query on product specification.
- Update shelf life specification to correspond with finished product specification.
คุณสมบัติ
- Bachelor’s degree in Pharmacy, Pharmaceutical Science,Science, Biotechnology
- Experience in Quality Control or Laboratory in Pharmaceutical industry will be advantage.
- Good command in English and computer literacy.
- Strong interpersonal and communication skill, Analytical skill.
- Persuasive abilities, Hands-on in all aspect of work.
- High responsible with the timeline commitment, Patient and positive thinking.
This position is assigned for handling of control specification and all procedure of QC part according to the established product specifications and procedures. Also keep compliance to ensure that the documents part for registration are correctly.
Responsibility:
- Verify finished product & shelf life specifications for new product and update dossier for current product.
- Provide product specifications, analytical method, equipment or provide comparison of specification and test method as client request.
- Prepare official finished product specification and analytical method.
- Prepare product control record/ COA.
- Prepare the dossier for regulatory submission and responsible for the regulatory query on product specification.
- Update shelf life specification to correspond with finished product specification.
คุณสมบัติ
- Bachelor’s degree in Pharmacy, Pharmaceutical Science,Science, Biotechnology
- Experience in Quality Control or Laboratory in Pharmaceutical industry will be advantage.
- Good command in English and computer literacy.
- Strong interpersonal and communication skill, Analytical skill.
- Persuasive abilities, Hands-on in all aspect of work.
- High responsible with the timeline commitment, Patient and positive thinking.