Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. The role: The Sr. Quality Inspector (Line Operations) is a member of the Finishing Quality Assurance Team reporting directly to the Quality Finishing Line Operations Supervisor. They are responsible for ensuring an acceptable quality level (AQL) for all GMP products produced on the finishing lines. In addition, they are expected to be able to effectively make risk-based quality decisions for issues that occur online. They are expected to contribute to an environment where teamwork and productivity are encouraged, and safety, identity, strength, purity, and quality (SISPQ) are reflected in the finished product. The working hours for this role are Monday-Friday 2:45p-11:15p
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED