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Responsible for commissioning, qualification, and validation support in a cGMP facility. Manages CQV projects, technical investigations, and creates documentation in compliance with regulations.

The FP&A Business Partner will support financial planning, forecasting, and performance analysis, serving as a liaison between Corporate Finance and business units.

The Scientist role focuses on supporting R&D in lentivirus production and CAR T cell therapy optimization, conducting experiments, and analyzing data.

The Director of Operations oversees cell therapy production, manages a large team, ensures compliance with cGMP, and drives operational excellence in a fast-paced biotechnology environment.

The Operations Associate performs manufacturing procedures in a cGMP environment, ensuring quality compliance and supporting the production of CAR-T products. Responsibilities include executing processes, documenting data, and collaborating within a production team.

The Batch Record & Document Coordinator manages batch record documentation, ensuring compliance, correctness, and communication within the organization, while supporting audits and corrections as needed.

The Principal Scientist focuses on advancing analytical innovation for developing pipeline therapies, enhancing analytical workflows, and ensuring regulatory compliance through proof-of-concept studies.

The Senior Procurement Contract Specialist negotiates contracts, ensures compliance, manages risks, monitors performance, and resolves issues, focusing on procurement for various functions.

The Associate Director will lead CMC drug development projects, ensuring adherence to scope, budget, and timeline while coordinating cross-functional teams and communication.

The Associate Director manages compliance risk assessments, audits, and monitoring activities, ensuring effective compliance programs and alignment of company policies.