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Manufacturing Technicians (Associates) for the Adjuvant Manufacturing Team

Do you have experience with downstream processing and thrive in a dynamic work environment?  Would you like to be part of a company helping our customers bring new advanced biological products to market? Then join an international company where everyone is responsible for delivering right on time as one team! 

With AGC Biologics increasing activities, we are looking for operators with experience preferably within API production or other areas within the pharmaceutical industry.  

AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 30 nationalities employed at our site in Copenhagen and the daily language is English. 

The Adjuvant Manufacturing Team  The Adjuvant Manufacturing team is part of the larger Manufacturing function, which are responsible for the production of Drug Bulk Intermediate (DBI) and Active Pharmaceutical Ingredient (API) for pre-clinical, clinical and commercial use.  

The team is under establishment and the manufacturing line is currently under construction. When fully staffed the department will consist of approx. 40 full time employees, covering shift supervisors, manufacturing specialist and manufacturing associates (operators). 

The team will operate under cGMP and be responsible for running our dedicated adjuvant manufacturing line, executing unit operations as buffer preparation, homogenization, filtration, tangential flow filtrations and filling operations. As well as securing the compliance framework around the department, covering daily documentation of the operations, establishment and maintenance of SOPs, training documentation, deviation and CAPA management.  

The position
As a Manufacturing Associate you will be part of a team that will be leading in manufacturing excellence, operating a very important part of our business.

You will be responsible for: 

  • Perform the daily manufacturing activities, operate manufacturing equipment and perform individual unit operations according to SOPs and Batch production records 
  • Document all daily work and use of equipment according to cGMP 
  • Secure that daily production targets are meet and that next shift are setup for success 
  • Perform work according to all AGC’s procedures and policies to secure that all work is performed safe, compliant and reliable 
  • Support and perform troubleshooting on process and equipment challenges 
  • Support equipment maintenance and calibration activities   
  • Support optimization and standardization of work processes 
  • If interested, author and update procedures and create logbooks  

Experience & competencies
The ideal candidate holds an Technical degree, has downstream processing experience and has previously worked in a manufacturing team operating under cGMP preferably within the pharmaceutical industry.

The ideal candidate for the position has several of the below competencies/experiences: 

  • 3+ years of experience from the pharmaceutical industry working in an cGMP environment 
  • Technical understanding of, tangential flow filtrations, solution preparation and lipid technologies is an advantage 
  • Experience with automated filtration systems and electronic batch records 
  • Experience with disposable manufacturing equipment  
  • Good communication skills (English) 
  • Structured and punctual 
  • Experience with Lean and a genuine interest in continues improvements  

AGC Offers  AGC Biologics offers a dynamic working place with good opportunities for working with a varied array of tasks and challenges. This opens many doors for personal development and for you to make a real difference towards both patients and customer. At AGC Biologics the work environment is informal and humor is part of the work day. We respect each other and our differences, and we help each other to reach deadlines together as one team. 

How to apply
Upload CV, motivation letter, references and criminal record via the link on this page, and do it as soon as possible. AGC Biologiscs is partnering with Adecco on this recruitment, so if you have any questions about the position, you can contact our recruitment team: 

Tasja Sejerup +45 3838 1135
Lotus Mølgaard +45 3838 1124

About AGC Biologics 
AGC Biologics (AGC) is a global Contract Manufacturing Organization (CMO) with biomanufacturing facilities in Europe, Japan 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.  
AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of AGC Biologics’ innovative approach to cell line and process development.  
Visit to learn why AGC Biologics is a World Leader in process development and contract manufacturing.

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