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Biotechnology Project Coordinator

2 months ago

Gladsaxe, Gladsaxe Municipality, Denmark AGC Biologics Full time
Job Role Overview

As a QC Coordinator at AGC Biologics, you will play a key role in supporting the production of biopharmaceuticals by performing analytical testing and validating various analytical procedures according to ICH guidelines.

Responsibilities
  • Represent QC Chemistry in Customer project teams and internal AGC QC analytical teams
  • Lead cross-QC Analytical project teams
  • Coordinate and maintain knowledge of QC Project milestones and Batch release schedules
  • Responsible for coordination and overall timeliness of analytic method validations in collaboration with QC Subject Matter Experts
  • Be Specification owner including establishment and update of Specifications
Requirements
  • MSc within Chemistry, Biochemistry or other relevant area with 2 - 6 years relevant experience or a PhD with 3 years relevant job experience
  • Ability to represent QC in Projects, Project Core Teams and Customer meetings
  • Fluent in written and spoken English
Company Overview

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service. 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 our website.