Monitor and schedule resources to ensure timely delivery. Leverage your experience by having scientific knowledge, reviewing prescription documents, diluting active ingredients to ensure that your product is manufactured to specifications.
Responsibilities:
Investigate and define any processes that are critical to T-cell production.
Plan, report and update standard operating procedures (SOPs) and manufacturing reports.
Ensure docility with the Quality Management System.
Analyse results, troubleshoot assays and solve problems.
Liaise with Facility Executives to coordinate manufacturing tasks and raw material warehousing.
Examine the manufacturing records.
Working in a cleanroom environment with manufacturing teams.
Requirements:
Knowledge of GMPs in accordance with EU, FDA and MHRA standards.
Excellent attention to detail and problem-solving abilities, as well as the ability to investigate and evaluate data.
