Senior Technician, Mammalian Manufacturing

AGC Biologics

København

On-site

DKK 480,000 - 640,000

Full time

4 days ago
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Job summary

AGC Biologics in Søborg, Denmark, seeks a Senior Technician for Mammalian Upstream Manufacturing. Join a fast-paced team executing seed train expansion through inoculation, bioreactor operation, and process monitoring in a GMP setting.

You will document activities and collaborate with QA/QC while supporting LEAN and 5S initiatives. The role emphasizes English communication, structured problem-solving, and teamwork in a highly skilled production environment with exposure to advanced bioreactor

Qualifications

  • Fluent in written and spoken English.
  • Experience in quality-focused production environments.

Responsibilities

  • Execute and support critical steps in mammalian Upstream production.
  • Operate bioreactors and monitor key process parameters.
  • Document production activities per GMP requirements.
  • Support onboarding and continuous improvement initiatives (LEAN/5S).
  • Collaborate with QA, QC, PE and Manufacturing Support to ensure compliance.

Skills

English fluency
Quality-focused
Team collaboration
Biotech background

Job description

Senior Technician, Mammalian Upstream Manufacturing

At AGC Biologics in Søborg, upstream manufacturing is where science becomes medicine. Every day, our teams work with advanced cell culture processes to produce biologic therapies that support patients around the world.

As a Senior Technician in Upstream Manufacturing, you will play a key role in executing and supporting critical steps in the mammalian cell culture production process. Working in one of Denmark’s most advanced GMP facilities, you will help ensure that complex biologic processes run safely, reliably, and with the highest quality standards.

This role offers the opportunity to work hands-on with modern bioreactor systems and cell culture technologies while collaborating with colleagues across manufacturing, science, and quality. Your expertise and attention to detail will contribute directly to delivering therapies for international biotech and pharmaceutical partners.

Where Bioprocessing Expertise Meets Daily Operations

Your work will be closely connected to the daily execution of upstream manufacturing activities. You will support the production process from early seed train expansion through inoculation and bioreactor operations, ensuring that cell culture processes run according to approved procedures and quality standards.

A typical week may involve preparing media and process solutions, operating bioreactors, monitoring key process parameters such as pH, temperature, and dissolved oxygen, and documenting production activities in accordance with GMP requirements. You will also contribute to troubleshooting process challenges together with Process Engineering and other support teams.

Beyond running production, you will play an important role in strengthening operational excellence on the shop floor. This includes supporting onboarding of new colleagues, contributing to continuous improvement initiatives such as LEAN and 5S, and collaborating with QA, QC, PLE, PE, and Manufacturing Support to maintain high process reliability and compliance.

A Team Built on Knowledge Sharing and Accountability

You will join a highly skilled upstream production team consisting of technicians and scientists who work in a collaborative and data-driven way. Knowledge sharing, ownership, and mutual support are key parts of how the team operates.

The environment is fast-paced and dynamic, but also structured and supportive. Colleagues help each other solve challenges, share expertise across functions, and continuously improve processes and ways of working.

You will work closely with experienced specialists across the organization, giving you exposure to both manufacturing operations and process science while developing your own expertise in upstream cell culture technologies.

The position follows a fixed two-week rotation, with working hours from 06:00 to 17:04:

  • Week 1: Monday, Tuesday, Friday, Saturday and Sunday
  • Week 2: Wednesday and Thursday

The schedule then repeats every two weeks

What Will Help You Succeed
  • We are looking for someone who enjoys working in a structured, quality-focused production environment and who takes pride in executing complex processes with precision.
  • You likely have a technical background as a Process Operator, Process Technologist, Industrial Operator, or similar, combined with experience from manufacturing environments such as biotech, pharmaceutical, or food production.
  • Experience with upstream processes such as seed train expansion, inoculation, bioreactor operation, or aseptic handling will help you quickly contribute to the team. Just as important, you are someone who collaborates well with colleagues, communicates clearly, and stays calm and structured when production schedules are tight.
  • Since procedures and documentation are handled in English, fluency in written and spoken English is required.
A Global Biotech Environment with Real Impact

AGC Biologics is a global Contract Development and Manufacturing Organization (CDMO) partnering with biotech and pharmaceutical companies to bring new biologic medicines to patients worldwide.

In Søborg, you will become part of an international production environment where innovation, quality, and collaboration drive everything we do. You will work with advanced technologies, experienced colleagues, and global clients developing the next generation of biologic therapies.

At AGC Biologics, we believe strong teams create strong results. That is why we focus on developing our people, improving our processes, and creating opportunities for employees to grow both technically and professionally.

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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