Not specified (assumed to be in-office based on the nature of the role).
Cgmp manufacturing experience
Upstream and downstream process knowledge
Cell culture and fill-finish operations
Esco Aster Pte. Ltd. is seeking a Manufacturing Biotechnologist with experience in cGMP environments to support the technology transfer and manufacturing execution of cell and gene therapy products. The role involves collaboration with multiple teams and requires strong leadership, communication skills, and a commitment to safety and compliance
Job Summary
The role supports the successful technology transfer and commercial readiness of cell and gene therapy products within a cGMP environment.
Candidates will serve as Manufacturing Subject Matter Experts during audits and lead commissioning, qualification, and process performance activities.
The position offers firsthand exposure to emerging modalities including cultivated meat certification and full cell line creation capabilities.
Matching Summary
Match Score: 85
Esco Aster Pte. Ltd. is seeking a Manufacturing Biotechnologist with experience in cGMP environments to support the technology transfer and manufacturing execution of cell and gene therapy products. The role involves collaboration with multiple teams and requires strong leadership, communication skills, and a commitment to safety and compliance.
Skills & Requirements
Must-have
cGMP manufacturing experience
Upstream and downstream process knowledge
Cell culture and fill-finish operations
Aseptic technique and cleanroom work
Batch record documentation and GDP compliance
Nice-to-have
Experience with autologous/allogeneic campaigns
Knowledge of USFDA, EU GMP, HSA GMP regulations
Strong leadership and communication skills
Ability to work independently under pressure
Familiarity with electronic batch records
Key Requirements
Minimum Bachelor's Degree in Biotechnology or related field
2-4 years experience in cGMP biologics or cell/gene therapy
Hands-on equipment experience in upstream/downstream processes
Proficiency in MS Office Suite and Good Documentation Practices