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Then Incyte is the pharmaceutical company for you. While our pipeline demonstrates the ability to compete with much larger pharmaceutical companies in selecting compelling targets and creating high-quality drug candidates, our smaller size enables employees to see the direct impact of their contributions on the direction of the company. Due to our smart, agile culture and cutting-edge science, we delivered a novel, first-to-market product in an unmet medical need in 2011 - the first in the company's history.

Opportunities for taking on new and/or additional responsibilities, in addition to advancement, are a key element in our culture. Add to that a science-based, fast-paced work environment and you’ve got an exciting company in which to work.

In addition to opportunities for growth, we offer an outstanding benefits andcompensation package to help meet personal needs as well.

Take a look at our current openings to find the match that’s right for you!

Incyte Corporation values the talents of our diverse workforce and is proud to be an Equal Opportunity Employer.

Automation MES Manager

Department: Biologics Commercial Manufacturing
Location: Incyte Biosciences Technical Operations Sārl - Yverdon

Job Summary  (Primary function)

The Automation MES Lead is responsible to develop, validate and support all the activities linked to the implementation of a Manufacturing Execution System (MES) for the Incyte Manufacturing site at Yverdon-les-Bains.

Essential Functions of the Job  (Key responsibilities)

  • Define a complete and detailed user requirement in collaboration with the key users
  • Follow up that all the tasks are performed on time with the appropriate level of quality by the local and external team
  • Ensure that the MES is configured in order to cover the data integrity requirement
  • Guarantee that all the validation is performed accordingly to the guidance and maintain this validation status among the time
  • Ensure that the system cover the user requirement defined at the beginning of the project
  • Ensure that the project is roll-out within the budget agreed
  • Ensure that MES is well interfaced with other systems
  • Ensure that all the SOP are created on time, with the appropriate level of detail
  • Provide the training material at least for the key users
  • Create and manage all the access and all the change request
  • Provide expertise and support to the different department whenever needed
  • Participate or lead to improvement project linked to MES
  • Ensure that the MES is maintained according to the procedure and that the periodic review is done as defined
  • Ensure that the system is ready for inspection at any time and provide support during inspections
  • Contribute positively to a strong culture of business integrity and ethics
  • Act within compliance and legal requirements as well as within company guidelines

Qualifications (Minimal acceptable level of education, work experience, and competency)

  • Must have at least 5 years’ experience working with automated system
  • Must have at least 3 years of experience in Biotechnology industries
  • Very good knowledge in Data integrity and Computerized system validation
  • Very good knowledge in GAMP (Good Automated Manufacturing Practices) and Commission & Qualification system
  • Knowledge in Data Historian

Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.

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