Jobs at Umoja Biopharma

The Logistics Associate manages outgoing shipments, supports supply chain activities, and collaborates with departments to ensure shipping needs are met. Responsibilities include maintaining compliance with shipping regulations and improving warehouse processes.

Perform and review QC microbiology testing and environmental monitoring for lentiviral vector manufacturing. Support method establishment, equipment qualification, microbial investigations, document generation, training delivery, sample shipping, and continuous improvement in a cGMP-regulated QC laboratory.

Support downstream manufacturing operations, focusing on purification processes and compliance with GMP. Execute buffer preparation, chromatography, and material management while adhering to quality systems and SOPs.

The Quality Assurance Specialist will support GMP operations, ensuring compliance, reviewing documents, providing on-floor quality support, and facilitating continuous improvement in manufacturing processes.

Oversee QC Analytical lab operations, ensure compliance with cGMP standards, lead a team, and drive improvements in quality and efficiency.

The Associate Scientist II will develop and execute UPLC methods, ensuring product quality, collaborating with teams, and maintaining detailed experimental records.

The Senior Manager, Quality Assurance Operations leads QA oversight at a biopharmaceutical facility, managing teams and ensuring compliance with regulations. Responsibilities include advancing quality culture, supporting audits, and developing strategies for execution.

The Vice President of Analytical Development will lead Umoja's analytical strategy, overseeing method development and regulatory submissions while ensuring operational excellence and team growth.