About the Company
Our client is a
global Contract Development and Manufacturing Organization (CDMO)
dedicated to advancing the development and production of biologic therapeutics. With world-class facilities and a commitment to innovation, quality, and collaboration, they provide
end-to-end biologics solutions –
from cell line and process development through to clinical and commercial manufacturing.
Their mission is simple yet powerful: to help biotech and pharma partners
bring high-quality, affordable biologics to patients faster
. Backed by deep technical expertise, operational excellence, and a partnership-first approach, they continue to expand their global reach and service portfolio in response to a dynamic and rapidly evolving industry.
The Opportunity
Overview
This is a senior leadership role responsible for overseeing all activities within the Purification Process Development Department, ensuring scientific excellence, operational efficiency, and alignment with company objectives. The Director will lead a team of scientists and engineers in the development, optimization, and scale-up of purification processes for biologics, while maintaining the highest standards of safety, quality, and compliance.
Key Responsibilities
- Supervise departmental personnel and resources to ensure all goals and objectives are achieved safely and efficiently.
- Lead the development, optimization, and scale-up of
purification processes
for biologics and related molecules. - Provide leadership in
incident investigation, troubleshooting, and root cause analysis
, ensuring timely and accurate reporting.
Ideal Candidate
- Master's Degree or above in Life Sciences / Chemistry / Pharmacology.
- 6+ year of related work experience in purification process development or tech transfer
- Rich experience in purification process development, tech transfer and scale up.
- Familiar with FDA, ICH, CDE related drug research and development quality research guidelines.
- Fluent in English