A growing biotechnology/life sciences company has an opening for a Sr. Process Engineer.  

Our client is a leading provider of products and services to accelerate development of viro-immuno-oncology drugs.

In this role your responsibilities will be to:

• lead transfer activities for formulation & filtration processes as they progress from execution in development lab to aseptic manufacturing


• serve as clinical manufacturing lead for aseptic pre-GMP and GMP batches


• support manufacturing of pilot scale development batches


• facilitate project communication and issue resolution with internal/external customers

• BS/BA in chemistry, biochemistry, chemical engineering, or related science with 5-8 years cGMP manufacturing experience in pharmaceutical/medical device/biotechnology


• A combination of experience and education may be acceptable


• Aseptic background is strongly preferred


• “Hands On” experience working in a lab/manufacturing area


• Previous experience w/ process development and process validation; technology transfer and process transfer


• Previous experience with biopolymers - Preferred!


• Previous experience in critical analysis of data (statistical software experience - Preferred!)


• Previous experience w/ continuous improvement/lean projects/programs - Preferred!


• Previous GMP manufacturing experience


• Qualities to be successful – Leadership skills – ability to take initiative, strong interpersonal skills, ability to coach and teach on development, collaborative team player- ability to create strong working relationships