Senior Technician – Mammalian Downstream Manufacturing (Night Shift)

AGC Biologics A/S; København; On-site; DKK 450,000 - 600,000; Full time

Benefits offered by this job

Pension

Health insurance

Canteen access

Employee Club

Employee discount

Job summary

AGC Biologics is seeking a Senior Technician for our Copenhagen Mammalian Downstream Manufacturing site. You will execute downstream purification processes, operate chromatography systems (UNICORN), ensure GMP-compliant documentation, and support deviations and continuous improvement.

This night-shift role (18:00-05:04 or 20:00-07:04) offers exposure to multiple products, coaching of colleagues, and a collaborative team culture with pension, health insurance, and other local benefits.

Qualifications

• 3-5 years of experience in GMP-regulated manufacturing, preferably biopharma.
• Educational background as Process Operator, Industrial Technician, Biotechnology Technician, or equivalent.
• Hands-on experience with chromatography, filtration, and UF/DF processes.
• Good understanding of UNICORN chromatography systems.
• Familiarity with GMP requirements, aseptic practices, and production documentation.
• Independent execution of complex manufacturing activities and problem solving.

Responsibilities

• Execute downstream purification processes, including chromatography, filtration, and UF/DF.
• Operate chromatography systems and apply technical knowledge during production.
• Ensure GMP documentation and compliance with procedures and aseptic practices.
• Support troubleshooting, deviation investigations, and continuous improvement.
• Own training, qualifications, and development.
• Share knowledge and train less experienced colleagues.
• Support development of new colleagues and uphold high GMP standards.

Skills

GMP experience

Purification processes

UNICORN systems

Chromatography

Documentation

Team training

Education

Process Operator qualification

Tools

UNICORN software

Job description

About the Job

As a Senior Technician, you will be responsible for executing downstream purification processes and ensuring that manufacturing activities are carried out safely, efficiently, and in compliance with GMP requirements. You will work independently within your area of expertise while collaborating with colleagues to meet production goals. The role requires strong process understanding, sound judgement, and the ability to adapt to different manufacturing setups without compromising quality.

Responsibilities

• Executing downstream purification processes, including chromatography, filtration, and ultrafiltration/diafiltration (UF/DF).
• Operating chromatography systems, including UNICORN software, and applying your technical understanding during production.
• Ensuring accurate GMP documentation and compliance with approved procedures and aseptic practices.
• Supporting troubleshooting, deviation investigations, and continuous improvement activities.
• Taking ownership of your training, technical qualifications, and development.
• Sharing knowledge and providing hands-on training and guidance to less experienced colleagues.
• As you become familiar with our processes, you will take an active role in supporting the development of new colleagues and contributing to high standards of technical performance and GMP behaviour within the team.

Who Are We Looking For?

• Have approximately 3-5 years of experience in GMP-regulated manufacturing, preferably within biopharmaceutical production.
• Have an educational background as a Process Operator, Industrial Technician, Biotechnology Technician, or an equivalent relevant technical qualification.
• Have hands-on experience with chromatography, filtration, and UF/DF processes.
• Have a good understanding of UNICORN chromatography systems.
• Are familiar with GMP requirements, aseptic practices, and accurate production documentation.
• Can independently execute complex manufacturing activities and contribute to solving technical challenges.
• Take ownership of their work and development, maintain high standards of quality, and contribute positively to the team.
• Work in a structured way, adapt to changing production needs, and willingly share knowledge.
• Communicate openly and understand when to ask for support or escalation rather than compromise quality or compliance.

Working Hours

This is a night-shift position (18:00-05:04 or 20:00-07:04) in our Mammalian Downstream Manufacturing department in Copenhagen. You will work according to an established shift schedule (5-2 in a 14 days period) supporting our manufacturing operations.

What We Offer

• An opportunity to work with different products and downstream manufacturing setups, developing your technical expertise.
• A role where your experience matters, both in daily production and in supporting the development of your colleagues.
• A supportive and approachable manager who values trust, accountability, and open communication.
• A collaborative team environment where knowledge sharing and continuous improvement are encouraged.
• An attractive compensation and benefits package, including pension, health insurance, and other benefits in accordance with local agreements.
• Access to our canteen arrangement, Employee Club, and employee discount opportunities.

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. 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. AGC Biologics is Your Friendly CDMO Expert – dedicated partners with the expertise and commitment to support our customers and teams. If you’re motivated by meaningful impact and ready to join our journey, we invite you to explore our current opportunities!