Looking for an exciting new career challenge?
Invenia Group is partnered with a growing viral vector CDMO start-up that has only recently emerged from stealth mode, who are seeking an experienced and driven professional to take on the role of Director of Quality Control & Analytical Development.
This individual will have experience in setting up a QC lab, cGMP & cGLP as well as method development & validation with a focus on Gene or Cell Therapy.
Skills & Experience Required:
- cGMP and cGLP experience.
- Setting up a QC lab or being heavily involved in the early stages of this process.
- Method development & Validation.
- Background in gene analytics, protein analytics, and general biological tests is a plus.
- Highly developed analytical skills
- Excellent planning skills
- Leadership
- Highly credible with good communication and interpersonal skills
- Excellent market knowledge
- A strong team player with the ability to work on their own initiative.
- Ability to relocate to Philadelphia (contribution by client)
Sound interesting? Apply to find out more.
