Automation Specialist (on-site)

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Automation Specialist (on-site)
Maintenance

This is an opportunity to join a newly build process facility with strategic importance to Xellia Pharmaceuticals and the objective to establish an aseptic API bulk handling facility. This means that you will have a major influence on getting the solutions to function optimal and make your mark on the final validation.
The automation scope is broad and contains milling, micronization, dispensing in isolator, utilities, HVAC, data collection, network, and production datacenter.

About the Department
You will be part of Technical Services’ BI, OT & Automation Team, responsible for our production systems in CPH. The team is diverse and consists of 12 dedicated colleagues of which four are also working with maintaining and developing automation systems. In the team, we emphasize always having a helpful and relaxed tone. Xellia offers a flexible working environment with the possibility of home office days. You will be dedicated to the project, but with strong roots in the automation team ensuring alignment and collaboration with colleagues
The project has its own project group, which you will be a part of. The group consists of both internal and external specialists working on the project.

The Position
We are looking for one fulltime employee to work on the project with the automation systems installed in the new facility. There will also be a need for integrating some of the system with existing Xellia infrastructure and service setup. This will be done together with others from the team and integrators.
As the SAP filling facility is part of a pharmaceutical production, it is built in relation to both GMP/FDA guidelines, which also means that testing, qualification, and documentation is an essential part of the job.
Taking your competences into account, you will be able to greatly influence your everyday life and the development of this position. We expect you to contribute with a systematic approach and be open and listen when retrieving information. Needless to say, you must have strong communicative skills and be able to work together with various people. It is important that you understand quality assurance and are passionate about doing things right.

Examples of specific tasks in the position include:

Automations Profile

  • specifications of interfaces between automation systems
  • review of FAT/IQ/OQ protocol and tests
  • contributions to FAT/OQ/OQ. (Travel activities 1-2 week per year)
  • creation of protocol and test plans for tests (Xellia scope)
  • execution of tests.

Qualifications
We expect you to:

  • have a strong automation profile with hands on experience, programming PLC, and SCADA systems (Siemens WinCC,or IFIX)
  • have hands on experience with RTU.
  • have a background as an engineer, cand. Scient, or equivalent. Maybe you come from a similar position or an operation position and want to try some more project related work for a period. Preferably with 3-5 years of experience from a similar position.
  • master English, both written and spoken. The Danish language would be a plus but not a must.

You are structured, engaged and thrive at a high pace. We also expect you to be able to commit yourself at all organizational levels and be a positive partner for our production units. As everyday life is changing in relation to the rate of production, it is important that you thrive on a changing environment and can take responsibility as well as show great flexibility and patience.

Contact and deadline
If you have any questions about the position, you are very welcome to contact Team Leader David K. B. Møller Phone no. +45 20220394 or Project Manager Christina Sindhøj Phone no. (+45) 41 31 76 73.

Please send your application as soon as possible and no later than 23 December 2022. Applications will be reviewed on an on-going basis, and interviews will be planned as soon as a suitable candidate is identified.

Xellia Pharmaceuticals is a specialty pharmaceutical company developing, manufacturing and commercializing anti-infective treatments against serious and often life-threatening bacterial and fungal infections. Headquartered in Copenhagen, Denmark, Xellia has a global footprint with R&D, manufacturing and commercial operations across Europe, Asia, the Middle East and North America. Xellia is wholly owned by Novo Holdings A/S and employs a dedicated team of over 1,800 people.
With over 115 years of experience, Xellia is a world-leading trusted supplier of several important established anti-infective drugs, comprising active pharmaceutical ingredients as well as injectable products. Continuing the Company’s evolution, Xellia is generating an innovative pipeline of value-added anti-infective medicines intended to enhance patient care, providing convenience and ease of use for healthcare professionals.
Together you can help us lead the fight against infections.
Further information about Xellia can be found at: www.xellia.com
Connect with us on LinkedIn


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Jobbet er oprettet på vores service den 1.9.2022, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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