*Senior Automation Engineer

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Are you interested in helping us digitalize and automate manufacturing processes, connect production data to our Data Lake, modify, upgrade, and maintain our diverse landscape of process control systems? Do you have a passion for leading the way to implement smarter production systems? Are you creative and able to think out of the box? Then you can assist us in improving automation processes and help us take the next steps in producing pharmaceutical products! As the Automation Engineer, you will lead the technical automation activities and solutions in supporting the current and future Automation/ IT Track lead for the large-scale multi-purpose facilities in our Copenhagen site.

About the department

You can look forward to becoming part of a dynamic and well-functioning team consisting of Process Engineers, Reliability Engineers, and Support Technicians. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with diverse stakeholders in the organization at site and global levels including Production departments, IT, MSAT, and QA. We enjoy contributing to a wide range of activities and projects within the organization. You will experience an enthusiastic working climate focused on quality, teamwork, and delivery. Your broad understanding of Automation/ IT technology will support and lead the way for how we handle Automation/ IT and further develop our platforms.

Your primary responsibilities will be:

  • Daily operational support, process information digitalization, and automation projects.

  • Assist with implementing changes and new process equipment, reviewing supplier documentation, producing qualification documentation, and conducting qualification and commissioning tests for the automation packages.
  • Handle inquiries from other technical leads on a daily related to onboarding of new automated process systems.
  • Perform routine maintenance and system administration tasks as needed across the diverse array of system under your care and responsibility needed for the upkeeping of a stabile production environment.
  • Participate in major Automation/IT projects at site and global level such as, implementation of Process Historian, Central Alarm Handling System, eBR/MES, S88/95 Bach Production, and digitalization of paper-based processes is among the many future projects you will actively participate and deploy across our different control platforms.

Desired Competencies:

  • 5+ years of experience as automation engineer, automation manager or work package owner from large pharma / biotech projects.
  • Solid experience with DCS systems, SCADA and PLC solutions, particularly Siemens PCS7, DeltaV, iFIX and Allen Bradley platforms.
  • Knowledge of batch processes, GMP, GAMP and the S88/S95 Batch standard.
  • Able to work under minimal supervision.
  • Ability to manage multiple, diverse projects with structure and coordination with manufacturing, IT, and other departments as needed to ensure there timely completion and within budget.
  • Great positive energy and courage to empower and inspire others.
  • Able to communicate with others in terms and manner conducive to their understanding of the problems and recommendations with our process control systems.
  • Ability to hold the role as technical lead and provide long term vision to better empower AGC in their use of process control systems.

In addition, you must thrive in a dynamic and fast-paced working environment where changes occur on short notice. The environment is dynamic and challenging at times, which requires finding solutions, delivering on promises, and giving our customers a positive experience. AGC has international customers, equipment suppliers and our company language is English. It is therefore a required ability that communication in both written and spoken English is fluent.

At AGC Biologics, you will get a unique opportunity working with a variety of different state of the art technologies among +40 different nationalities. This opens many doors for personal and professional development and for you to make a real difference towards patients, our customers, and your personal and professional growth. AGC offers an informal working environment, characterized by the fact that we think it is fun to go to work. We respect each other and our differences. AGC employees are flexible and take pride in working together to achieve goals as one team.

Applications are screened on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation for applying to this position.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i København

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

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