Support Sterility Assurance assessment in regulated manufacturing industry.Experience in Environmental qualification and Contamination control Strategy.Experience in aseptic process simulation risk assessment, validation strategy and oversight.Experience in Contamination control strategy of pharmaceutical sterile products.Execution of sterilizing equipment qualification.Experience in microbiological and biological method application and validation.Participates in cross functional projects, including customer meetings.Participates in the writing of protocols, reports, and specifications.Drives deliverables to completion with structured timelines.Requested Qualifications :Degree in microbiology, biology, biotechnology or science-related field.Understanding of good documentation practices and general quality laboratory function.Ability to work independently.Strong attention to details, organizational skills and drive to be successful.Experience with aseptic technique and biological safety cabinets.Essential : Proficient in spoken and written English and / or a native language.Able to travel domestically and internationally if required.J-18808-Ljbffr
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