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Open nowPosted 5 days ago

OT Operations Specialist

AGC Biologics34 open roles

Where
Copenhagen, Denmark
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Your applicationOpen nowOT Operations SpecialistAGC Biologics · Copenhagen, Denmark

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. AGC Biologics postings stay open a median of 24 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 5 days ago

AGC Biologics median: 24 days open

The posting

Location: Søborg, Denmark. Please note that AGC Biologics does not offer relocation assistance. Applicants must already reside in Denmark or the Greater Malmö area in Sweden.

At AGC Biologics, we are constantly developing our manufacturing capabilities to support the delivery of life-changing biologics to patients worldwide. As our new OT Operations Specialist, you will play an important role in maintaining and improving the Operational Technology landscape that supports our GMP-regulated manufacturing environment.

You will work at the intersection of technology, manufacturing, and quality, ensuring that our systems are reliable, compliant, and ready to support future digitalization initiatives. This role offers the opportunity to work with advanced manufacturing technologies while collaborating with experts across Automation, Engineering, Manufacturing, Quality, and IT.

A key role in our Operational Technology landscape

As a OT Operations Specialist, you will help ensure stable and compliant manufacturing systems while supporting continuous improvements across our digital production environment.

Your responsibilities will include:

Operational Technology

  • Support and maintain OT infrastructure and manufacturing systems in a GMP-regulated production environment.
  • Manage OT servers, virtualization platforms, industrial networks, and system integrations.
  • Troubleshoot complex OT-related issues across manufacturing environments.
  • Collaborate closely with Automation, Engineering, Manufacturing, Quality, and IT teams to ensure reliable operations.

GMP & Compliance

  • Ensure OT systems remain compliant with GMP requirements and data integrity principles (ALCOA+).
  • Drive and support Change Controls (CRs), Deviations, CAPAs, and Risk Assessments related to OT systems.
  • Support audits, inspections, and periodic system reviews.
  • Contribute to Computer System Validation (CSV) activities, including IQ/OQ documentation and execution.

Digitalization & Integration

  • Support integration between manufacturing systems and business systems.
  • Participate in digitalization initiatives involving MES, Historian, SCADA, ERP, and related manufacturing platforms.
  • Support industrial communication technologies such as OPC UA, Modbus, and Profinet.
  • Drive continuous improvements and identify opportunities for automation and increased operational efficiency.

Security & Lifecycle Management

  • Support OT cybersecurity initiatives and contribute to maintaining a secure technology environment.
  • Manage system lifecycle activities including upgrades, patching, backup, disaster recovery, and access management.
  • Ensure systems remain secure, reliable, and inspection-ready.

A collaborative environment with room to make an impact

You will join a team where collaboration, knowledge sharing, and continuous improvement are key parts of how we work. You will work closely with colleagues across different functions and act as a trusted technology partner to Manufacturing, Engineering, Quality Assurance, and IT.

Success in this role means maintaining a stable and compliant OT environment, driving GMP-related improvements, strengthening system integrations, and identifying opportunities where technology can improve our manufacturing processes.

We are looking for someone who brings

You have a strong interest in combining technology with manufacturing and thrive in an environment where quality, compliance, and reliability are essential.

We imagine that you have:

  • A Bachelor's degree in Engineering, IT, Automation, Computer Science, or a similar field.
  • 5+ years of experience within OT, Manufacturing IT, Automation, or Life Sciences.
  • Strong understanding of GMP-regulated environments.
  • Experience managing Change Controls, Deviations, CAPAs, and validation activities.
  • Experience working with OT infrastructure, servers, virtualization, and industrial networking.
  • Experience working with manufacturing systems such as SCADA, Historian, MES, or similar platforms.
  • Strong stakeholder management and communication skills.

It is an advantage if you have experience with:

  • MES platforms and manufacturing system integrations.
  • APIs and data flows between systems.
  • Industrial communication protocols such as OPC UA, Modbus, or Profinet.
  • OT cybersecurity frameworks and best practices.
  • Supporting FDA, EMA, or other regulatory inspections.

Why join AGC Biologics?

At AGC Biologics, you will have the opportunity to shape the future OT landscape and digital manufacturing strategy while working in a highly regulated and technologically advanced production environment.

You will collaborate with talented colleagues across a global organization where innovation, knowledge sharing, and continuous improvement are part of everyday life. Your work will directly contribute to ensuring reliable manufacturing processes that help bring important biologic therapies to patients worldwide.

Join our team

We are eager to welcome a new colleague as soon as possible. Please submit your application no later than 15 November 2026. Applications are reviewed on an ongoing basis, and we reserve the right to close the vacancy before the deadline if a suitable candidate is found.

If you have any questions about the position, please contact Jimmy Jespersen, Director of IT, at [email protected]

Please apply exclusively through our recruitment system. Applications submitted through other channels will not be considered.

To support an inclusive and unbiased recruitment process, please do not include a photo in your CV. At AGC Biologics, we are committed to fair hiring practices and value diversity and inclusion throughout our recruitment process.

Please note that AGC Biologics does not offer relocation assistance. Applicants must already reside in Denmark or the Greater Malmö area in Sweden.

We look forward to receiving your application!

Who We Are AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Denmark. From our Søborg site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

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