Analytical Research Engineer 分析研发工程师
人福普克药业(武汉)有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2017-06-09
- 工作地点:武汉
- 招聘人数:5人
- 工作经验:3-4年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位月薪:4-6千/月
- 职位类别:医药技术研发人员 药品生产/质量管理
职位描述
职位描述:
Essential Responsibilities:
1. Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance; Ensure work accomplish on time, correctly and in compliance with relevant SOP's;
在较少的帮助下为各个项目提供高效扎实的专业技能;确保工作在遵循SOP的前提下准确、按时完成;
2. Display basic technical understanding of related disciplines, conduct routine /non-routine research and design experiments with some support;
对相关学科有基本的技术性的理解,在一定的指导下组织常规/非常规的研究和实验设计;
3. Provides assistance and interpretation of project results to team members and technical support to QC and MFG;
为组员提供帮助和实验结果的解读,为QC和生产部提供技术支持;
4. Work on the bench (e.g. developalidate analytical methods, adapt new technologies) with a focus on chromatography (HPLC, GC), titration and various spectroscopic methodologies (e.g. IR );
该岗位主要是色谱分析(HPLC,GC)、滴定及各种光谱法(如红外),例如分析方法开发及验证,适用新技术等;
5. Develop and validate analytical methods, create all necessary data and write protocol/report for ANDA/NDA products registration and method transfer to production units;
开发和验证分析方法,记录所有必需的实验数据并撰写ANDA/NDA注册产品的方案及报告、方法转移;
6. Understand and apply interpretation of analytical methods and determination of stability indicating analytical methods, including HPLC chromatographic separation, UVisible absorption, Gas chromatography, to ensure appropriate testing is conducted to fully characterize stability profile of products;
理解并应用分析方法和稳定性指针分析方法(包括HPLC、UV、 GC),确保采用了合适的测试方法表征了产品所有的稳定性特征;
7. Participate in investigations of deviation as author.
组织偏差调查。
Qualifications:
1.Bachelor degree or above, with the major in Pharmaceutical Analysis is preferred
本科及以上学历,药物分析专业优先考虑;
2.Minimum of 3 years’ experience in the pharmaceutical industry or development groups;
3年以上在制药行业或开发团队的工作经验;
3.Experience with variety of analytical techniques, method development and validation: HPLC, GC, UV, FTIR, Karl-Fischer moisture analysis.
拥有各种分析技术、方法的开发和验证的经验;
4.Excellent record keeping skills
优秀的存档记录技能;
5.Ability to follow directions
遵从上级指示;
6.Excellent team and interpersonal skills
优秀的团队和人际交往技能;
7.Strong attention to detail
注重对细节的处理;
9.Good command of English
熟练掌握英语;
10.Familiar with Quality Control laboratories and procedures.
熟悉质量控制实验室及其程序。
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Essential Responsibilities:
1. Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance; Ensure work accomplish on time, correctly and in compliance with relevant SOP's;
在较少的帮助下为各个项目提供高效扎实的专业技能;确保工作在遵循SOP的前提下准确、按时完成;
2. Display basic technical understanding of related disciplines, conduct routine /non-routine research and design experiments with some support;
对相关学科有基本的技术性的理解,在一定的指导下组织常规/非常规的研究和实验设计;
3. Provides assistance and interpretation of project results to team members and technical support to QC and MFG;
为组员提供帮助和实验结果的解读,为QC和生产部提供技术支持;
4. Work on the bench (e.g. developalidate analytical methods, adapt new technologies) with a focus on chromatography (HPLC, GC), titration and various spectroscopic methodologies (e.g. IR );
该岗位主要是色谱分析(HPLC,GC)、滴定及各种光谱法(如红外),例如分析方法开发及验证,适用新技术等;
5. Develop and validate analytical methods, create all necessary data and write protocol/report for ANDA/NDA products registration and method transfer to production units;
开发和验证分析方法,记录所有必需的实验数据并撰写ANDA/NDA注册产品的方案及报告、方法转移;
6. Understand and apply interpretation of analytical methods and determination of stability indicating analytical methods, including HPLC chromatographic separation, UVisible absorption, Gas chromatography, to ensure appropriate testing is conducted to fully characterize stability profile of products;
理解并应用分析方法和稳定性指针分析方法(包括HPLC、UV、 GC),确保采用了合适的测试方法表征了产品所有的稳定性特征;
7. Participate in investigations of deviation as author.
组织偏差调查。
Qualifications:
1.Bachelor degree or above, with the major in Pharmaceutical Analysis is preferred
本科及以上学历,药物分析专业优先考虑;
2.Minimum of 3 years’ experience in the pharmaceutical industry or development groups;
3年以上在制药行业或开发团队的工作经验;
3.Experience with variety of analytical techniques, method development and validation: HPLC, GC, UV, FTIR, Karl-Fischer moisture analysis.
拥有各种分析技术、方法的开发和验证的经验;
4.Excellent record keeping skills
优秀的存档记录技能;
5.Ability to follow directions
遵从上级指示;
6.Excellent team and interpersonal skills
优秀的团队和人际交往技能;
7.Strong attention to detail
注重对细节的处理;
9.Good command of English
熟练掌握英语;
10.Familiar with Quality Control laboratories and procedures.
熟悉质量控制实验室及其程序。
职能类别: 医药技术研发人员 药品生产/质量管理
公司介绍
人福普克药业(武汉)有限公司是设在美国新泽西州的普克医药公司(PuraCap Pharmaceutical LLC)引进美国***制药技术和美国FDA CGMP质量标准,在武汉生物医药产业园投资建立的高质量的国际制药企业,产品涵盖多种剂型的美国处方药/非处方药,面向欧美主流市场。 本公司具有世界级的管理团队和技术力量,有良好的企业文化和发展前景,提供专业培训和有竞争力的待遇,诚邀有志制药行业发展的各位英才加盟,共同打造世界级制药企业。
公司将提供优厚的福利待遇:
薪酬:有竞争力的薪酬(含绩效奖金及年终奖金)
福利及休假:试用期内开始为员工办理五险一金+定期体检+国家法定假日+一年12天带薪年假(入职即可享受)
交通及食宿:工作餐,为外地或倒班员工提供宿舍
其它:定期组织丰富多彩的员工活动
公司将提供优厚的福利待遇:
薪酬:有竞争力的薪酬(含绩效奖金及年终奖金)
福利及休假:试用期内开始为员工办理五险一金+定期体检+国家法定假日+一年12天带薪年假(入职即可享受)
交通及食宿:工作餐,为外地或倒班员工提供宿舍
其它:定期组织丰富多彩的员工活动
联系方式
- 公司地址:地址:span武汉市东湖高新开发区光谷生物城生物医药园高新大道神墩二路99号
- 电话:18271875661