MBR Design Engineer

Overview Summary

As Engineer MBR Design, you will ensure the configuration and parametrization, the improvements and the support of MES system (Manufacturing Execution System) within the respect of GMP requirements linked to this system.

Within the frame of activities of Yverdon’s site, The Engineer MBR Design designs the required manufacturing processes in MES (MBR) following established rules.

The Engineer MBR Design supports the Engineering group with the MES activities (routine’s activities and qualification’s activities). Participate to MES activities management linked to manufacturing.

DUTIES AND RESPONSABILITIES

Realize the MES MBR and update the related master data if required in respect of manufacturing planning. Drive and support the MBR release planning to deliver on time the required MBR for manufacturing activities (routine production, tech transfer). Drive the review and technical approval of MBR with Manufacturing, Manufacturing Technology and Quality teams. Create and manage deviations, investigations and CAPA related to MBR. Create and manage change controls and change actions related to MBR. Support Manufacturing team and Quality team as MES technical expert for quality events and support proactively the MBR continuous improvement. Maintain and improve manufacturing operational knowledge with a regular presence on the manufacturing floor and participation in key manufacturing meetings and decisions. Participate to MES improvement projects (e.g. interfaces to other systems like SAP, LIMS, PCS) to improve the manufacturing processes and support digitalization. Write and update MES SOP and MES training materials. Train MES users. Participate to MES On-Call service. Participate to audits in case of MES subjects.

Bachelor’s Degree in relevant field such as pharmacy, biotechnology, chemistry, or equivalent experience in the pharmaceutical industry. Thorough knowledge of biotechnological technologies, processes, with a demonstrated experience in computerized and MES systems (PAS-X is a plus). Must speak English and French. Excellent written and verbal communication skills. Must have minimum of 5 years in an MBR creator/MES Admin role in a biopharmaceutical manufacturing environment Demonstrated proficiency in good practice requirements GMP as well as biopharmaceutical industry regulations and standards related to quality, qualification and validation¨ Be able to work within a highly controlled and demanding environment. The ability to make pragmatic and compliant decisions Strong result orientation and committed team member

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.

We Respect Your Privacy Learn more at: http://www.incyte.com/privacy-policy

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here. You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is