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UID158282
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积分681
注册时间2014-1-26
最后登录1970-1-1
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本人不才,在医药圈混了了不到10年,英文自我感觉还可以,所以求外企验证兼职工作。以下为个人工作能力简介,有意者站内短信联系。谢谢关注。
Preparing Validation Master Plan
 Providing timely updates to the client.
 Completing timesheets and expense reports in a timely manner.
 Working in a biotech/pharmaceutical environment as a consultant/contractor for various clients
 Working closely with client's employees on various projects and various GMP facilities to help client with validation issues.
 Learning new ideas, techniques and systems.
 Commuting to clients' manufacturing for validation projects.
 Keep client’s proprietary information confidential.
 Writing Validation Protocols such as DQ,IQ, OQ and PQs
 Executing Validation Protocols such as IQ, OQ and PQs
 Calculating and interpreting of collected data from validation studies.
 Generating Validation Summary Reports and Standard Operating Procedures(SOPs)
 Create Validation Risk Assessments
 Mentoring junior staff and interns |
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