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Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry 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. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.

In this role, you will have the opportunity to:

1、Manage the whole process of infrastructure projects, including application, design, construction, construction and acceptance；

2、Carry out project schedule, quality, security, cost and other work to achieve the purpose of project control；

3、Responsible for managing and coordinating the overall process of the project construction site and checking the engineering settlement

4、Participate in project bidding, provide relevant information for bidding and do a good job in coordination

5、Participate in the internal audit of construction plan and provide suggestions

6、Responsible for organizing the weekly meetings and coordination meetings of all concerned, and doing well the work of organizing and coordinating on the project site;

7、Responsible for external technical cooperation and communication between the company and related construction side

8、Coordinate with the main contractor and supervising unit to deal with on-site problems;

9、Check the quality of construction , and organize professional engineers to provide technical support;

10、Responsible for collecting, sorting and filing of information during the process of project

The essential requirements of the job include:

1. Proficient in spoken English2. GMP FDA industry background with 5 years of management experience in ISO 5.0&A/B level clean workshops3. CAD (necessary) 3DInfant (optional)4. Undergraduate or above5. Background of LEADER processing NC CAPA6. Background for writing URS, validation plan, and summary validation report7. Project Coordination (mandatory) Project Management (optional)8. Familiar with GB54057 cGMP ISO14644 standard

   It would be a plus if you also possess previous experience in:

2. Public system management personnel in biopharmaceutical factories - manufacturing；

2.Microelectronics or chip clean workshop manufacturing plant

3.Foreign automobile manufacturing plants, project management, infrastructure management

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.