UlliSupport Sterility Assurance assessment in regulated manufacturing industry. /liliExperience in Environmental qualification and Contamination control Strategy. /liliExperience in aseptic process simulation risk assessment, validation strategy and oversight. /liliExperience in Contamination control strategy of pharmaceutical sterile products. /liliExecution of sterilizing equipment qualification. /liliExperience in microbiological and biological method application and validation. /liliParticipates in cross functional projects, including customer meetings. /liliParticipates in the writing of protocols, reports, and specifications. /liliDrives deliverables to completion with structured timelines. /li /ulpbRequested Qualifications : /b /pulliDegree in microbiology, biology, biotechnology or science-related field. /liliUnderstanding of good documentation practices and general quality laboratory function. /liliAbility to work independently. /liliStrong attention to details, organizational skills and drive to be successful. /liliExperience with aseptic technique and biological safety cabinets. /li /ulpuEssential : /u Proficient in spoken and written English and / or a native language. /ppAble to travel domestically and internationally if required. /ppJ-18808-Ljbffr /p #J-18808-Ljbffr