Technician, Manufacturing (Night Shift)

AGC Biologics; København; On-site; DKK 320,000 - 420,000; Full time

Job summary

AGC Biologics is a global CDMO with GMP production of biologics at Søborg, Denmark. As a Manufacturing Technician, you join an international team responsible for mammalian core buffer operations, with a 5:2 pattern and 18:00–05:00 schedule.

You will work under English-only procedures, collaborate across teams, and support audits. The role requires flexibility and commitment to permanent night shifts and weekend work.

Qualifications

• You have an operator/technical/laboratory background with GMP experience.
• Proactive team player; flexible and positive.
• Able to follow written procedures in English.
• Independent work capability with task responsibility.
• Experience in clean rooms and audits/inspections.

Responsibilities

• Prepare and filter buffers; scale from small to large.
• Plan daily line work; order materials and approve buffers.
• Use simple analytical methods (pH, conductivity, osmolality).
• Transport and sanitize production equipment and disposables.
• Monitor equipment and room conditions daily.
• Shift schedule includes day/evening/night/weekend shifts.

Skills

GMP experience

English proficiency

Team player

Procedural compliance

Tools

Clean room

Job description

Working hours

This is a permanent night shift position with the following schedule:

• Working hours: 18:00–05:00

Before you apply

Working hours

This is a permanent night shift position with the following schedule:

• 5:2 shift pattern
• Working hours: 18:00–05:00
• Weekend work is included

Please only apply if you are able to work this schedule on a permanent basis.

Language Skills

Proficiency in English is a requirement for this position. We only accept CVs and applications written in English. Applications submitted in any other language will not be considered.

Please note that an English exercise is included as part of the recruitment process.

Location

Relocation support is not available for this position. We can therefore only consider applicants who are already based in Denmark or the Greater Malmö area.

About The Job

Join a dynamic and international company.

At AGC Biologics, we develop biopharmaceutical processes and run GMP production of proteins and cells, from early state test until commercial production. As we are a Contract Development Manufacturing Organization (CDMO), the customer is in centrum, and we have a high level of service to our customers.

The department

As our new technician in Manufacturing you will be part of a professional and dedicated team consisting of both scientists and technicians. You will experience a very dynamic working environment with a high variety of tasks, and an environment where cGMP production never becomes routine.

We work in close collaboration with other teams and departments who are dependent on the solutions and services we deliver.

Responsibilities And Tasks

As member of our Mammalian Core Buffer Team you will work with:

• Preparation and filtration of buffer solutions from small scale (< 5 kg) to large scale (up to 2000 kg).
• Daily planning of work on the line, ordering of raw materials and disposables if needed and approval of finalized buffers.
• Simple analytical methods as pH, conductivity, osmolality etc.
• Transport and surface sanitization of production equipment and disposables.
• Daily control and responsibility for equipment and rooms.

The work will be on day/evening/night/weekend shift according to shift plan.

We are continuously working on improvements and optimization of existing processes and routines and support a strong learning environment where we within relatively short time, become familiar with a variety of new processes and technologies.

Experience And Competencies

You have an operator/technical/laboratory background, GMP experience, is a proactive team player, flexible, positive and you:

• Can work according to written procedures in English.
• Can work independently and with responsibility for own tasks.
• Have experience with work in clean rooms.
• Can work in an organization with constant customer audits and inspections.

As our corporate language is English, all our procedures and GMP related documents are in English. It is therefore important that you can read English without problems, and we also appreciate the ability to speak English.

Application deadline: 30 August 2026.

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.