Aseptic Process Development - CDMO
External
Medvacon · Indianaplos, INPrepare for this interview
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About the role
Direct the development and establishment of processes in GMP. Accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. Provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders. If you're interested so far - apply! A member of our talent team will contact you and share comprehensive job details. Bachelors Degree 5+ years exp in a cGMP pharma/biotech setting Solid foundation in the fundamentals of biochemical engineering, virology and cell biology Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations Experience with cell culture technologies, molecular biology, and aseptic processing Please attach a WORD resume to your submission All of your information will be kept confidential according to EEO guidelines. ON-SITE only This is a FT role and will include a full benefits package 40-hour week NO AGENCIES please
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