CQV Manager [Denmark]


 

Are you an experienced CQV Manager with an ability to manage design activity and technical concepts which are state-of-the-art in the pharmaceutical industry?

Do you thrive in an international environment where we design and build the world’s most challenging projects together with our clients?

Do you want to be part of a building the presence of Fluor Corporation in Denmark?

Then you might be our new colleague! We are looking for a CQV Manager to join our team at Fluor’s Nordic Technology Hub in Copenhagen.

Fluor Corporation has established a Technology Hub in Copenhagen to service the Nordic countries. Our office in Portland Towers is brand new and we are hiring some of the brightest professionals who take pride in delivering top-notch services and solutions to our clients. We are looking for the “first movers” who get excited about building Fluor’s reputation in the Nordics, the ones who enjoy teamwork and know that good relationships and respectful communication with clients and colleagues is the foundation for successful project execution. We build our culture on trust, diversity, and flexibility to work from where the need is, because we believe that our employees’ well-being is also our responsibility. You will be part of something big as Fluor employs over 40.000 people globally - but our Copenhagen family is still small but growing.

To be Considered Candidates:

Must be authorized to work in the country where the position is located.

Basic Job Requirements

The position is newly established and reports directly to the Director of the Nordic Technology Hub. The CQV Manager oversees all regulatory compliance activities on key, strategic projects including the review of engineering and operating documents for manufacturing and utility systems. You will lead the regulatory compliance, qualification, and validation discipline for the projects in the Nordics. You will be part of an international management team working both virtually and face to face in Denmark. This role will establish and review policies for Current Good Manufacturing Practices (cGMP) compliance of engineering, procurement, fabrication, construction, manufacturing, validation (EPFCMV) practices within Fluor.

Other Job Requirements

The CQV Manager is the primary responsible person for the CQV packages and discipline assigned to him/her working in close collaboration with the Construction and Engineering teams. This means that you will be implementing and supervising the technical quality and ensuring that our technical solutions adhere to requirements from our clients, comply with regulatory standards and finally also fulfill our internal company regulations/guidelines for example the validation master plan. You will play a key role when evaluating new technology and/or material to determine their suitability for the use in (future) manufacturing processes. This role interfaces with the different offices in Europe to leverage the overall CQV knowledge in Fluor to deliver successful project performance. Finally, the CQV Manager develops new approaches to work processes and project execution.

Qualifications needed
  • You hold a Bachelor or Master’s degree within engineering or another relevant field
  • You have approximately 10-15 years of experience in a similar role from the Life science industry
  • You must be fluent in written and spoken English language. Knowledge of Danish is an advantage.
  • You possess good listening skills and able to put yourself in the shoes of our clients, vendors, and other collaboration partners to understand their needs
  • You are a strong communicator which enables you to get your messages across effectively
  • Finally, you enjoy working in an international environment with colleagues from around the world

Requisition Number

140858BR

Diverse Workforce

We are an equal opportunity employer that recognizes the value of a diverse workforce. All qualified individuals will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, genetic information, or any other criteria protected by governing law.

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