Upstream Process Development Specialist

2 days ago


Copenhagen, Copenhagen, Denmark AGC Biologics Full time

We are looking for an experienced Upstream Process Development Specialist to join our Clinical Team in Manufacturing Product Support department. As a key member of our team, you will be responsible for developing and implementing upstream processes for clinical products, ensuring compliance with GMP regulations.

The ideal candidate has experience working in a cGMP environment and is familiar with Good Manufacturing Practices (GMP) and applicable regulations. They should also have strong technical problem-solving skills and the ability to coordinate multi-departmental tasks.

Main Responsibilities:

  • Develop and implement upstream processes for clinical products
  • Ensure compliance with GMP regulations
  • Collaborate with cross-functional teams to develop and implement process improvements
  • Train technicians on new processes

About Our Company:

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO). 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.

We value personal initiative and professional achievement, and offer a competitive compensation package and a friendly, collaborative culture. AGC Biologics is an equal opportunity employer, committed to diversity and inclusion.



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