The chance to impact a dynamic workforce to offer strategic support with some of the leading SMEs and Large Pharma companies as an external partner to the pharmaceutical industry. Providing knowledge on broad range of drug substances (from small molecules to synthetic oligonucleotides to biologicals) and drug products (from solid orals to sterile solutions to nanoparticulate formulations), you will join this Global leader as a CMC consultant.
- Experience with CMC and regulatory requirements for all development stages, from pre-clinical to Phase III or commercial
- Ph.D. or master's degree in Pharmacy, Chemistry, Biopharmaceuticals, Biochemistry, Biology or comparable
- At least five years in a scientific/technical CMC development or CMC - regulatory affairs function
- Willingness to travel moderately (Meetings with clients, agencies or CMOs)
Please don't hesitate to apply below or contact with your updated CV and availability to speak.