Technician, QA Manufacturing Support

AGC Biologics, Inc.; København; Hybrid; DKK 420,000 - 540,000; Full time

Job summary

AGC Biologics in Søborg, near Copenhagen, is seeking a QA Manufacturing Support Technician. You will support the Manufacturing Batch Release process, review batch documentation and ensure GMP compliance, while working close to the production line and collaborating with QA and Manufacturing teams.

You will review solution preparation documentation, support scanning/archiving tasks, and help connect QA with production to maintain traceable, compliant records on the floor.

Qualifications

• Bachelor's degree or equivalent in science or technical field.
• Experience with GMP/GLP production environments.
• Experience reviewing Batch Production Records and Solution Preparation Sheets.

Responsibilities

• Perform QA Oversight in the Solution Preparation production suite.
• Review and approve Buffer and Media Batch Production Records.
• Print Batch Process Records and manage manufacturing labels.
• Provide real-time review of manufacturing records and logbooks.

Skills

QA oversight

Documentation review

GMP knowledge

Communication skills

Education

Bachelor's degree in science

Job description

Technician, QA Manufacturing SupportWe use cookies to make the safest and most effective website possible.# AGC Biologics## Technician, QA Manufacturing SupportApply: Copenhagen, Denmark: Full time: Posted Yesterday: End Date: November 13, 2026 (12 days left to apply): JR103186**QA Manufacturing Support Technician****Be close to production and make a difference in quality every day** At AGC Biologics in Søborg, Quality and Manufacturing go hand in hand. As our new QA Manufacturing Support Technician, you will play an important role in supporting manufacturing activities during solution preparation and ensuring that production documentation meets GMP requirements.This position offers an exciting combination of working close to the production line and handling batch record reviews and buffer and media documentation. You will be an important link between QA and Manufacturing, helping to connect the two functions and support a smooth and compliant manufacturing process. **Where Quality meets Manufacturing**In this role, you will support the Manufacturing Batch Release process by ensuring that solution (media and buffers) batch documentation are reviewed in accordance with established procedures and GMP requirements. Your daily responsibilities will include:* Performing QA Oversight in the Solution Preparation production suite in VAT83B.* Supporting manufacturing during review of batch documentation, including questions related to Good Documentation Practice.* Reviewing and approving Buffer and Media Batch Production Records.* Printing Batch Process Records and managing manufacturing labels.* Providing real-time review of manufacturing records and logbooks. You may also support scanning, archiving and other related activities when needed.What makes this position particularly interesting is the opportunity to combine documentation review with direct interaction with production. You will be close to daily manufacturing activities while contributing to the Quality processes that support batch release. **A dynamic team with strong connections to production** You will become part of a dynamic and proactive QA team consisting of 7 Scientists and 4 Student Assistants.The team works closely with Manufacturing, and collaboration is an important part of everyday work. Together with your manager and colleagues, you will help build strong connections between QA and Manufacturing, acting as a bridge between the teams.This is a role for someone who enjoys being involved in daily operations, working with different colleagues and combining structured documentation tasks with close collaboration on the production floor. **Bring your attention to detail and collaborative mindset**We imagine that you hold a Bachelor's degree (BSc) or a qualification as a Technician in production. Ideally, you have experience from a GMP or GLP production environment or a QA department within the biopharmaceutical industry.You bring an interest in, or previous experience with, reviewing Batch Production Records and Solution Preparation Sheets.Strong communication and collaboration skills are important, as you will work with colleagues and stakeholders across functions. You are fluent in written and spoken English and communicate clearly with both internal and external stakeholders. As a person, you have a positive mindset, are flexible and enjoy taking on new tasks and responsibilities. You thrive in a dynamic environment and are comfortable navigating uncertainties. **Interested in joining our team?**We will review applications as they arrive, so please submit your application and CV as soon as possible.We look forward to hearing from you.**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.*