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
Job details are sourced from the employer's original posting.
Open job postingAbout the company
MEDVACON Life Sciences works with many leading pharmaceutical companies to hire temporary and full-time employees to join their organization. We're providing hiring support for our pharma client located in Foster City, CA for 2 Research Assocaites in the Foster City location.