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Senior QC Manager for Gene Therapy Products
1 week ago
About MeiraGTx
We believe temporal control of gene therapy products has the potential to transform the gene therapy landscape. Our state-of-the-art manufacturing facility was designed to meet global regulatory requirements, including current good manufacturing practices (cGMP) required by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK and the U.S. Food and Drug Administration (FDA). The facility has the flexibility and capacity to produce sufficient product for all our clinical trials and will scale to commercial capacity.
Job Requirements
- Degree in a relevant scientific discipline or equivalent experience.
- 7+ years of experience working in a Pharmaceutical/Biotech QC function within a sterile manufacturing site.
- Experience managing a team in a cGMP QC analytical environment.
- Excellent collaboration, communication, and conflict resolution skills.
- Experience in audit inspections.
- Good technical writing skills.
- Natural curiosity and desire to learn and understand systems and processes.
- Ability to work in a fast-paced environment.
