Join a growing CMC Operations group . . . .

The qualified candidate will be responsible for the process development, process scale-up and manufacture of small molecule drug substance material via external laboratories (CRO's CDMO's).

To qualify, your skills should include:

• Developing and implementing drug substance manufacturing processes (small molecule).
• Ability to manage outsourced cGMP manufacturing.
• Knowledge of regulatory requirements for drug substance submissions.

Would you like to learn more?

Call: 978.686.2200 OR

Schedule a call: https://calendly.com/richconnors OR

Email: rich@vista-technology.com

Visit our Company Website - www.vista-technology.com

Visit our Career Opportunities Page - www.biopharmaceuticaljobs.net