Job Description

Job Description ResponsibilitiesAssemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.Follow standard work instructions and interpret technical drawings to ensure consistent product quality.Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.Complete all relevant training before performing any task.Timely completion of relevant batch records with adherence to Good Documentation Practice (GDP).Participate in Practical Process Improvements (PPI) to improve production efficiency and product quality.Adhere to all safety protocols and guidelines to maintain a safe working environment.Work collaboratively with team members, including engineers, quality assurance, and maintenance personnel.Communicate effectively with supervisors and colleagues to ensure smooth production operations.Ensure accurate storage and handling of materials to prevent contamination or damage.Perform any other duties as assigned by the Manager.