Senior Technician, Quality Control

at  AGC Biologics

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
The Department
The QC organization consists of five departments: QC Bioassay, QC Chemistry, QC Microbiology, QC support and QC planning & systems. QC are responsible for release testing of clinical and commercial batches, and validation of the analytical methods, as well as analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.
The current position in located in QC Bioassay group, in Søborg, Denmark. QC Bioassay is responsible for supporting the production of new biopharmaceuticals by performing analytical testing and validating various analytical procedures according to ICH guidelines and regulatory bodies from early phase to commercial. QC Bioassay Cell and Reference material have a close collaboration within the QC area and with department across the organization.
Roles and responsibilities
As a Cell-based assay technician you will be a part of a dedicated team with highly competent colleagues focusing on Cell-based assays. You will be involved in multi-disciplinary projects working in close collaboration with team members and/or in project groups across the QC Bioassay Cell based assays groups responsibilities.

The main tasks will be the following:

• Routine maintenance of cell lines
• Testing of release and stability samples in cell-based assays
• Validation of cell-based assays
• Daily housekeeping of cell laboratory
• Documentation according to our quality system GDP/GLP/GMP
• Responsible for analytical equipment i.e. keeping log books, ensure service has been performed etc.
• Working according to cGMP
• Be able to utilize new knowledge quickly and have good communication skills

You can look forward to a great deal of responsibility and varied work tasks. You can also look forward to being part of a really good team in an open and informal environment with solid professionalism, high pace and lots of good laughs.
Your profile
The ideal candidate holds a degree as technician (laborant) or equivalent, and has a minimum of 3-5 years of work experience in analytical development or quality control. We expect you to have a structured mindset, be able to work independently and meet tight deadlines with a can-do attitude, but without compromising the quality.

In addition, we expect you bring some of the following experience and characteristics:

• Experience within Cell-based assays
• Experience working in a Cell laboratory
• Experience working in a GMP environment
• Good communication skills and a service-minded attitude as you will work closely with different stakeholders
• The ability to handle multiple tasks simultaneously in a busy environment
• Fluent in written and spoken English

Join an international and agile organization
At AGC, you will get great opportunities to work with a wide array of tasks and challenges, and you will get experience with our various departments. Furthermore, as we plan projects and tasks together in the team, you will get the opportunity to influence your daily work. AGC offers an informal working environment where high energy and enthusiasm is part of the daily work life. We respect each other and our individual differences. At AGC, we have a flexible attitude, and we help each other reach deadlines as a team.
Contact and application
For any further questions, you are more than welcome to contact Manager Ann-Louise Theis Littau phone 26830439 or email: atlittau@agc.com. Please be aware that we take in consideration only the applications send via our career page and, not via email. We will process the applications as they arrive.
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AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy, and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.
Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on
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AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances

• Routine maintenance of cell lines
• Testing of release and stability samples in cell-based assays
• Validation of cell-based assays
• Daily housekeeping of cell laboratory
• Documentation according to our quality system GDP/GLP/GMP
• Responsible for analytical equipment i.e. keeping log books, ensure service has been performed etc.
• Working according to cGMP
• Be able to utilize new knowledge quickly and have good communication skill