Aseptic Process Development - CDMO
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.
Qualifications
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
Additional Information
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