海翱思（大连）食品安全研究有限公司
2010-12-13
基本信息
| 所在地区 | 辽宁省大连市 | 单位地址 | 大连经济技术开发区双D港 | 隶属部门 | 辽宁省 |
| 联系部门 | 办公室 | 单位电话 | 联 系 人 | ||
| 单位性质 | 其他企业 | 单位传真 | |||
| 单位网址 | 电子邮件 | healthfoodsafetylab@ | 单位邮编 | 116620 | |
| 备 注 | |||||
需求信息
| 落实毕业生方式 | 个人自荐 | ||||||||||
| 提 供 待 遇 | |||||||||||
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单位简介
海翱思（大连）食品安全研究有限公司简介
海翱思（大连）食品安全研究有限公司位于大连经济技术开发区双D港，是国内首家按照美国食品和药品管理局（FDA）和欧盟食品安全局（EFSA）GLP规范和标准进行管理和运作的，从事国际食品安全检测的独立的第三方食品安全测定公司。公司业务是根据美国FDA、欧盟EFSA食品安全标准，对中国出口美国、欧盟和世界其它国家的食品及对在华的国外食品生产企业的产品提供安全检测服务。同时，为中国食品生产商提供国际食品安全标准的咨询和相关技术改进服务。
公司为员工提供系统的FDA / EFSA法规和标准的培训，提供外派到北美公司学习和培训的机会。同时，公司提供广阔的个人发展空间、 激励性薪酬保障体系和完善的个人职业发展规划。
公司目前招聘以下职位的技术。请符合条件者将个人简历和二寸免冠照片发至Email：healthfoodsafetylab@。
二、招聘岗位
1、职务描述: 食品测定工程师10名
对申请者要求
学历要求:本科及以上
专业要求:分析化学/食品分析/药物分析/环境分析/生物化学和分子生物学
工作经验描述：具备药物或化学成份的色谱质谱分析基础，从事过残留或相关分析、熟练操作GC/MS，HPLC/MS/MS，ICP-MS者优先。
具GLP实验操作经验和知识者优先
英语口语和书写能力好
职位的主要职责和能力:
按SOP要求进行食品分析
执行GLP规范
撰写分析报告，向负责经理汇报分析结果
完成负责经理布置的工作
2、Position: Principal Scientist/Study Director（部门经理）2名
Qualification:
M.Sc or B.Sc in analytical chemistry, food analysis, biochemistry / molecular biology, related organic analytical chemistry
Hands-on experience in food analysis or related laboratory work
Demonstrated analytical chemistry problem-solving and troubleshooting abilities, proven HPLC, GC, GC/MS and/or LC/MS/MS methodology and analytical techniques, assay validation
Strong planning, organization and communication abilities including English communication skills (in particular in writing English)
Ideally with exceptional GMP and GLP compliance knowledge
Duties:
Provide overall management of selected projects
Liaise with study sponsors worldwide
Prepare study proposals and provide scientific input of study design
Coordinate with study team members to execute study
Provide scientific advice and assistance to team members when required
Provide training to new employees when needed
Comply with GLP guidelines
Prepare study reports
Report to the management team
Providing training
3、 QA / QC Manager（质量控制（QC）/ 质量确认（QA）经理职位）2名
Qualification:
Master or Bachelor degree in a science related field (food, chemistry, life sciences).
Bio-analytical laboratory experience preferred
GLP experience and knowledge is preferred, but training in China and/or Canada / USA will be provided when needed
Ability to organize and manage priorities to meet deadlines
Communication skills (oral and written) in English and Chinese
Ability to maintain and control document systems
Duties:
Maintaining and revising the quality assurance policies and procedures developed as part of the quality program for the company.
Providing compliance support (e.g., GLPs, SOPs, Good Documentation)
Reviewing protocols and protocol amendments
Reviewing and revising standard operating procedures
Conducting study and facility inspections to review work in progress
Auditing raw data and study reports to assure they reflect the methods and procedures used
Writing and issuing QA audits to Management, Principal Investigators and Study Directors
Reviewing deviations/investigations and assisting in the improvement of internal procedures
Supporting regulatory/client audits, as needed
Ability to interpret regulatory compliance and explain it to others
Ability to deal effectively with analysts, Principal Investigators, Study Directors and Management
Providing oversight that the appropriate internal and external compliance is maintained by performing specific departmental audits
Cooperating closely with the management to prepare prior to and during all audits from clients and/or applicable regulatory agencies
Reviewing the various study protocols, study reports, and related documents generated throughout the company to assure internal external compliance with procedures.
Reviewing and maintaining control of equipment use, calibration, and maintenance documents.
Assuring documents are appropriately archived.
Reviewing technical publications, articles, and abstracts to stay abreast of the regulatory and quality developments within the industry.
Helping analyze and resolve or assist personnel in solving quality-related problems.
Providing training as necessary to other employees related to quality systems.
Understanding and following all procedures and processes required for work performed under the appropriate regulatory bodies.
海翱思（大连）食品安全研究有限公司位于大连经济技术开发区双D港，是国内首家按照美国食品和药品管理局（FDA）和欧盟食品安全局（EFSA）GLP规范和标准进行管理和运作的，从事国际食品安全检测的独立的第三方食品安全测定公司。公司业务是根据美国FDA、欧盟EFSA食品安全标准，对中国出口美国、欧盟和世界其它国家的食品及对在华的国外食品生产企业的产品提供安全检测服务。同时，为中国食品生产商提供国际食品安全标准的咨询和相关技术改进服务。
公司为员工提供系统的FDA / EFSA法规和标准的培训，提供外派到北美公司学习和培训的机会。同时，公司提供广阔的个人发展空间、 激励性薪酬保障体系和完善的个人职业发展规划。
公司目前招聘以下职位的技术。请符合条件者将个人简历和二寸免冠照片发至Email：healthfoodsafetylab@。
二、招聘岗位
1、职务描述: 食品测定工程师10名
对申请者要求
学历要求:本科及以上
专业要求:分析化学/食品分析/药物分析/环境分析/生物化学和分子生物学
工作经验描述：具备药物或化学成份的色谱质谱分析基础，从事过残留或相关分析、熟练操作GC/MS，HPLC/MS/MS，ICP-MS者优先。
具GLP实验操作经验和知识者优先
英语口语和书写能力好
职位的主要职责和能力:
按SOP要求进行食品分析
执行GLP规范
撰写分析报告，向负责经理汇报分析结果
完成负责经理布置的工作
2、Position: Principal Scientist/Study Director（部门经理）2名
Qualification:
M.Sc or B.Sc in analytical chemistry, food analysis, biochemistry / molecular biology, related organic analytical chemistry
Hands-on experience in food analysis or related laboratory work
Demonstrated analytical chemistry problem-solving and troubleshooting abilities, proven HPLC, GC, GC/MS and/or LC/MS/MS methodology and analytical techniques, assay validation
Strong planning, organization and communication abilities including English communication skills (in particular in writing English)
Ideally with exceptional GMP and GLP compliance knowledge
Duties:
Provide overall management of selected projects
Liaise with study sponsors worldwide
Prepare study proposals and provide scientific input of study design
Coordinate with study team members to execute study
Provide scientific advice and assistance to team members when required
Provide training to new employees when needed
Comply with GLP guidelines
Prepare study reports
Report to the management team
Providing training
3、 QA / QC Manager（质量控制（QC）/ 质量确认（QA）经理职位）2名
Qualification:
Master or Bachelor degree in a science related field (food, chemistry, life sciences).
Bio-analytical laboratory experience preferred
GLP experience and knowledge is preferred, but training in China and/or Canada / USA will be provided when needed
Ability to organize and manage priorities to meet deadlines
Communication skills (oral and written) in English and Chinese
Ability to maintain and control document systems
Duties:
Maintaining and revising the quality assurance policies and procedures developed as part of the quality program for the company.
Providing compliance support (e.g., GLPs, SOPs, Good Documentation)
Reviewing protocols and protocol amendments
Reviewing and revising standard operating procedures
Conducting study and facility inspections to review work in progress
Auditing raw data and study reports to assure they reflect the methods and procedures used
Writing and issuing QA audits to Management, Principal Investigators and Study Directors
Reviewing deviations/investigations and assisting in the improvement of internal procedures
Supporting regulatory/client audits, as needed
Ability to interpret regulatory compliance and explain it to others
Ability to deal effectively with analysts, Principal Investigators, Study Directors and Management
Providing oversight that the appropriate internal and external compliance is maintained by performing specific departmental audits
Cooperating closely with the management to prepare prior to and during all audits from clients and/or applicable regulatory agencies
Reviewing the various study protocols, study reports, and related documents generated throughout the company to assure internal external compliance with procedures.
Reviewing and maintaining control of equipment use, calibration, and maintenance documents.
Assuring documents are appropriately archived.
Reviewing technical publications, articles, and abstracts to stay abreast of the regulatory and quality developments within the industry.
Helping analyze and resolve or assist personnel in solving quality-related problems.
Providing training as necessary to other employees related to quality systems.
Understanding and following all procedures and processes required for work performed under the appropriate regulatory bodies.
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