MEDVACON Life Sciences works with many leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.

Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.

Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their Indianapolis site.  This is a full-time role directly with the client - an outstanding opportunity to join an innovative company developing brilliant biotechnology.

A successful background will be strong in Lab, Process and Analytical development including working knowledge of cGMPs related to the production of viral therapeutics and the ability to interface successfully with multi-disciplined teams.

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