Manufacturing Support Technician

Krystal Biotech, Inc is seeking a highly motivated Manufacturing Support Technician to support our commercial manufacturing facility in the South Side. The Technician will work closely with the manufacturing team to uphold cleanroom standards, follow strict procedures, and contribute to the smooth operation of all manufacturing processes. Primary Responsibilities: * Assist in the setup, breakdown, and cleaning of equipment and manufacturing areas before and after production runs * Collaborate with manufacturing and quality teams to ensure that facilities are prepared and ready for production activities as per schedule * Execute and maintain strict cleaning and sanitization protocols in compliance with current Good Manufacturing Practices (cGMP) guidelines and Standard Operating Procedures (SOPs) * Conduct routine inspections of cleanrooms to identify any cleanliness or contamination issues, promptly reporting and addressing them according to established procedures * Follow and document all procedures, including batch records, cleaning logs, and any other required documentation accurately and in a timely manner * Adhere to safety protocols and guidelines, including proper handling and disposal of hazardous waste materials * Support the maintenance of process gas levels, calibration of equipment, and preventative maintenance schedules * Participate in training sessions and meetings to stay updated on the latest industry standards, regulations, and best practices * Assist with movement of materials; work with EHS/Materials Teams for collection and dispensing of biohazardous waste * Support a standard 40-hour work week with flexibility to support occasional off-shift hours and/or weekends * Perform other tasks, as assigned Requirements and Preferred Qualifications: * High school diploma or equivalent is required; additional technical or vocational training in biopharma manufacturing, cleanroom operations, or related fields is a plus * In lieu of direct experience, bachelor’s degrees in applicable fields such as life sciences or engineering will be considered * Experience with sanitization, aseptic technique and/or sterile processes in a regulated setting (GMP, ISO) is highly preferred * Ability to follow detailed instructions and maintain accurate documentation * Excellent attention to detail, organization skills, and the ability to prioritize and multitask effectively in a fast-paced environment * Demonstrated commitment to safety protocols and adherence to standard operating procedures * Excellent communication and the ability to work well both independently and as part of a team * Physical stamina and the ability to stand, bend, and lift heavy objects when necessary * Flexibility to work shifts, including evenings, weekends, and holidays as required.