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Danaher Corporation QC Engineer in Beijing, China

Be part of something altogether life-changing!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.

The QC Engineer for Cytiva is responsible for developing and implement testing, sampling and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met. Investigates and troubleshoots functionality and performance problems. Recommends corrective action when appropriate. May monitor and execute on-site equipment and tools calibration.

This position is part of the QC located in Beijing plant and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

1.Responsible for the relevant inspection of raw materials, process products, and finished products, as well as the monitoring of public systems, clarifying inspection standards and requirements.

  1. Responsible for measuring and managing inspection instruments and equipment.

  2. Responsible for the management of departmental documents and records.

4.Responsible for departmental verification, review, and other related work.

  1. Review and approve inspection reports for raw materials, process products, and public systems, as well as fill out and review laboratory records.

    The essential requirements of the job include:

  2. Bachelor's degree or above in pharmacy, food, and chemical related majors.

2.More than 3 years of laboratory work experience, such as in pharmaceutical plant, food plant, etc.

3.Have GMP related knowledge, familiar with clean area requirements, understand metrology related knowledge.

4.Proficient in listening, speaking, reading, and writing English, able to communicate normally in English.

5.Proactive in work, with good communication, thinking, and teamwork spirit, adept at learning new knowledge.

In this role, you will have the opportunity to:

1.负责原辅料、过程产品、成品的相关检验和公用系统的监控,明确检验标准和要求。

2.负责部门文件和记录的管理和培训;

  1. 负责部门验证、审核等工作。

3.审核、批准原辅料、过程产品、公用系统的检验报告和对实验室记录的填写和复核。

4.负责QC日常运行工作,包括检验数据收集分析、记录资料管理、保证试验环境、OOS和OOT调查、5S、DM、物资采购管理、安全管理等。

The essential requirements of the job include:

1.大学本科及以上学历,药学、食品、化工类相关专业;

2.3年以上实验室工作经验,如药厂、食品厂等;

3.有GMP相关知识,熟悉洁净区要求,了解计量相关知识.

4.熟练英语的听、说、读、写能力,能进行正常英语沟通。

5.工作积极主动,良好的沟通、思维、团队合作精神,善于学习新知识。

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

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