Senior Automation Engineer to Support on-going Operation and Modification Projects

Would you like to be a part of AGC Biologics growing success?

At AGC Biologics A/S we work with development and GMP manufacturing of APIs for both commercial products and products in all clinical phases. We are a client centric CDMO, and the partnership with our clients, working side by side with the clients, is our focus.

We are looking for a Senior Automation Engineer to support automation systems related to our on-going operation and various re-build projects. We will during 2024 have two manufacturing facilities to operate when our new EUR 160 million Mammalian Manufacturing Facility is getting into operation – and you will play an important role.

The department

You will be part of the Plant engineering department with focus on operation of all utility, maintenance, calibration and technical projects across our facilities. The department consist in total today of around 45 employees with managers, engineers, project managers, compliance specialist and technicians.

The position

You will ensure that AGC requirements are fulfilled for our automation systems. SCADA process control system is related to a range of utility systems and FMS for monitoring e.g. critical temperatures in rooms and freezers.

You manage effectively the communication between the counter part in the engineering company and internal stakeholders involved in the project.

You ensure that all work carried out and installation implemented is safe, effective and in compliance with the appropriated industry standards and authority regulations.

You ensure that company and site policies and procedures are adhered to.

You work closely with other stakeholders in the organization.

Your profile

Relevant Engineering degree.

5+ years of experience in the biopharmaceutical industry including experience working under GMP.

Experience from maintenance and troubleshooting of automation systems.

Hands-on experience with the similar automation system mentioned above.

You have experience in writing standard operating procedures.

The ability to work effectively under pressure and good flexibility to meet demand in the role.

Good communication skills – including the ability to communicate clearly and professionally in written and spoken English and Danish is preferred.

Good technical knowledge of pharmaceutical facility.

Knowledge of the qualification process for pharmaceutical manufacturing facilities.

How to apply
Send your application as soon as possible. We process the applications as we receive them and qualified applicants can expect to be interviewed before the deadline.

If you need further information about the position, please feel free to contact Thomas Østergaard, Manager in Plant engineering +45 27602130.

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.

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