Matica Biotechnology is at the forefront of biopharmaceutical research and development. The Matica Bio team brings an average of 15 years of cell and viral vector manufacturing experience to the development and manufacture of advanced therapy products. At our purpose-built GMP facility in College Station, Texas, we provide rapid development and scale-up of cell and gene therapies, vaccines, and Oncolytics meeting worldwide regulatory compliance.
The true value of a CDMO is determined by the quality of its people. Matica Bio consists of a dedicated team of experts. We’re a cell and gene therapy CDMO powered by people, and our people provide real benefits to the quality, safety and speed of the cell and gene therapy development pathway. Our inventive thinking and foresight help us strategize the best path to take therapies from the lab to the market. Come join our dedicated team and Make it Happen With Matica Bio!

• Provide subject matter expertise to the Quality Control organization to ensure that teamwork, high morale, and innovation are fundamental components of a world-class team
• Be able to multi-task and perform Analytical Test Methods with high accuracy and precision while also handling other cGMP activities like Deviations, Out of Specification Investigations and Validation activities.
• Lead investigations into deviations, non-conformances, or quality-related issues, and perform root cause analysis (RCA) to determine corrective actions.
• Implement continuous improvement initiatives to drive Quality Control programs and ensure maximum productivity.
• Collaborate with clients to develop and customize testing protocols based on specific regulatory or product requirements.
• Review and approve all QC-related documentation, including test results, deviation reports, and stability data.
• Create active training and development plans for Quality Control staff with the objective of driving the overall competence and professionalism of the Quality functions