Manufacturing Specialist

We are seeking a Manufacturing Specialist to support cGMP biopharmaceutical manufacturing operations with a focus on upstream virus production and downstream purification processes. This role will be responsible for executing manufacturing activities, supporting process operations, maintaining GMP documentation, and ensuring compliance with quality and safety requirements. Key Responsibilities: Perform hands-on upstream and downstream manufacturing operations in a cGMP environment Prepare media, buffers, and manufacturing support materials Set up, operate, and maintain bioprocess equipment and chromatography systems Pack chromatography columns for clinical and commercial manufacturing campaigns Support process monitoring, production activities, and technology transfer initiatives Assist with deviation investigations, data analysis, and manufacturing troubleshooting Review batch records, SOPs, and manufacturing documentation for accuracy and compliance Maintain equipment logs, production records, and GMP documentation Follow safety procedures and support continuous improvement initiatives Qualifications: Bachelor's Degree in a scientific or engineering discipline 2–5 years of manufacturing experience in a cGMP environment Experience with upstream processing, downstream purification, or bioprocess manufacturing Strong knowledge of GMP documentation and batch record review Excellent organizational, analytical, and communication skills #J-18808-Ljbffr United Pharma