Offer summary
Qualifications:
Masters or PhD in relevant field, Eight-plus years in biopharmaceutical industry, Experience in downstream process development, Expertise in downstream unit operations, Understanding of regulatory requirements.
Key responsabilities:
- Support downstream process development strategy and execution.
- Provide direction to CMOs and external labs for project performance.
- Oversee technical issue resolution and process validation activities.
- Manage data preparation for regulatory submissions.
- Create technical documents and enhance team collaboration.