Rydalmere药厂招聘QA Associate
公司名称
Pharmaceuticals
工作性质
全职
学历要求
Bachelor
签证要求
不限
工资水平
面议
工作亮点
团队友善,成长空间
公司地址
59 Kirby St
公司简介
Our company is a successful Australian manufacturer with multiple businesses awards. We specialise in manufacturing Health Supplements (complementary medicines and supplementary food) and Skin Care products.
工作介绍
KEY RESPONSIBILITIES:
1. Assist with all QA/QC daily operations including:
• Inspect and release incoming materials
• Inspect and perform in-process production check
• Inspect and release finished products
• Create and maintain production batch records, raw materials master files
• Perform or coordinate physical / microbial / chemical tests
2. Maintain QA system in compliance with TGA GMP and NSW HACCP, including:
• Create and maintain SOPs and Site Master File and formulations and specifications
• Perform internal and external GMP / HACCP audits
• Train all relevant personnel on GMP / HACCP
• Equipment and process validations
3. Perform and maintain Stability Program
4. Liaise with suppliers and customers on technical issues including formulations, quality, stability
5. Coordinate / perform / assist with product registration include research therapeutic functions of new products and prepare and submit ARTG listing application
8. Formulation R & D for new Pharmaceuticals / Cosmetic / Dairy products.
9. Assist with preparing and checking text for products brochures and labels.
10. Support other departments on technical and quality issues.
ESSENTIAL SKILLS AND COMPETENCIES:
1. Must have tertiary qualifications in Chemistry, or Microbiology, or Pharmacology, or GMP.
2. Experience in GMP / HACCP is preferred but not essential as training will be provided.
3. Good communication skills and eager to learn
4. Work as a Team with Can-Do attitude and creative thinking
1. Assist with all QA/QC daily operations including:
• Inspect and release incoming materials
• Inspect and perform in-process production check
• Inspect and release finished products
• Create and maintain production batch records, raw materials master files
• Perform or coordinate physical / microbial / chemical tests
2. Maintain QA system in compliance with TGA GMP and NSW HACCP, including:
• Create and maintain SOPs and Site Master File and formulations and specifications
• Perform internal and external GMP / HACCP audits
• Train all relevant personnel on GMP / HACCP
• Equipment and process validations
3. Perform and maintain Stability Program
4. Liaise with suppliers and customers on technical issues including formulations, quality, stability
5. Coordinate / perform / assist with product registration include research therapeutic functions of new products and prepare and submit ARTG listing application
8. Formulation R & D for new Pharmaceuticals / Cosmetic / Dairy products.
9. Assist with preparing and checking text for products brochures and labels.
10. Support other departments on technical and quality issues.
ESSENTIAL SKILLS AND COMPETENCIES:
1. Must have tertiary qualifications in Chemistry, or Microbiology, or Pharmacology, or GMP.
2. Experience in GMP / HACCP is preferred but not essential as training will be provided.
3. Good communication skills and eager to learn
4. Work as a Team with Can-Do attitude and creative thinking
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最新评论(1)
lveric
13天前
0
大药厂呀,厉害。请问可以兼职不?
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