Smithfield 悉尼西区制药厂招聘质量监管文件助理2名
该招聘企业尚未提供合法ABN,请慎重判断
公司名称
Carelife Nutrition
工作性质
全职,兼职
经验要求
不需要
学历要求
Bachelor
签证要求
不限
性别要求
不限
工资水平
面议
工作亮点
公司简介
制药厂招聘质量监管及文件管理人员1名,全职或兼职。
要求基本数字计算能力,化学或制药学历背景。
开车通勤。
工作介绍
Quality Assurance Assistant / Document Controller - Complementary Medicine Manufacturing
Lavida Pharmaceuticals a full suite of manufacturing solutions for therapeutic and non-therapeutic products: Our mission is to exceed customer expectations and act with integrity, excellence, responsibility with regards to everything that we do. In order to maintain our culture of continuous improvement and to assure quality throughout the manufacturing process, we are now seeking a Quality Assurance Assistant / Document Controller to join the team and assist the Quality Manager in all relative aspects.
The successful person will be an integral part of the company while contributing to improving all facets of our Quality System and production floor.
The Main Responsibility:
1. Assist QA Manager with creating, managing and overseeing Quality/Manufacturing documents, to ensure the proper documents are created and signed, that all data is accurate and that documents are stored and backed up.
2. Assist QA Manager with updating quality/production documents in compliance to standards,
3. Assist with updating WIs, SOPs and digital data base.
Skills and Experience:
1. Qualifications in Science related to pharmaceutical manufacture, e.g. chemicals, pharmacy, & science etc,
2. Well developed interpersonal skills and strong attention to detail,
3. Be able and comfortable to work on numbers and do basic math.
4. Prior experience in a QA position in a manufacturing environment would be highly regarded,
5. A basic knowledge of TGA and GMP,
6. Be comfortable and have flexibility to meet the demands set by daily changing priorities,
You will have a personal interest in remaining compliant with local and international authorities to further your knowledge.
Lavida offers exciting opportunities for personal and professional growth, if this sounds like your position, please send resume to hr@la-vida.com.au.
Lavida Pharmaceuticals a full suite of manufacturing solutions for therapeutic and non-therapeutic products: Our mission is to exceed customer expectations and act with integrity, excellence, responsibility with regards to everything that we do. In order to maintain our culture of continuous improvement and to assure quality throughout the manufacturing process, we are now seeking a Quality Assurance Assistant / Document Controller to join the team and assist the Quality Manager in all relative aspects.
The successful person will be an integral part of the company while contributing to improving all facets of our Quality System and production floor.
The Main Responsibility:
1. Assist QA Manager with creating, managing and overseeing Quality/Manufacturing documents, to ensure the proper documents are created and signed, that all data is accurate and that documents are stored and backed up.
2. Assist QA Manager with updating quality/production documents in compliance to standards,
3. Assist with updating WIs, SOPs and digital data base.
Skills and Experience:
1. Qualifications in Science related to pharmaceutical manufacture, e.g. chemicals, pharmacy, & science etc,
2. Well developed interpersonal skills and strong attention to detail,
3. Be able and comfortable to work on numbers and do basic math.
4. Prior experience in a QA position in a manufacturing environment would be highly regarded,
5. A basic knowledge of TGA and GMP,
6. Be comfortable and have flexibility to meet the demands set by daily changing priorities,
You will have a personal interest in remaining compliant with local and international authorities to further your knowledge.
Lavida offers exciting opportunities for personal and professional growth, if this sounds like your position, please send resume to hr@la-vida.com.au.
今日评论
网友评论仅供其表达个人看法,并不表明网站立场。
最新评论
暂无评论
看了又看
新鲜新闻