GENERAL RESPONSIBILITIES:
? Coordinate and carry out process design, development, scale-up and cGMP
production of clinical materials
? Independently design and execute purification steps for recombinant
proteins.
? Develop in-process characterization methods
? Supervise people within the Process Biochemistry group.
? Provide materials for methods development, product and process
characterization, validation and clinical grade materials
? This position is primarily hands-on bench work involving problem solving
and troubleshooting
REQUIREMENTS/QUALIFICATIONS:
? MS or BS level with minimum of 5 years work experience. Recent Ph.D. with
an internship or prior GMP Pilot/Process Development work experience
? Candidate must have a broad-based background in purification technology;
candidates with fluidized bed experience may receive preference
? Must be able to sequence protein purification steps in such a way that the
steps are compatible
? Experience in all or a combination of: Process Development, Protein
purification &/ characterization, GMP Clinical Production for protein-type
vaccines/therapeutics
? Prior experience with Baculovirus, Yeast and/or E. coli systems
Our client has therapeutics and vaccines in the market and a strong pipeline
of products in various stages of development and clinical trials. Non-PhDs
have the ability for strong career growth with our client. The company has
both a scientific and management track that does not limit a person based on
degree.
If you have an interest in this or other opportunities, please email your
resume as an attached file or mail/FAX your CV/resume to RS&A to the
attention of Ann G. Rathbun, Managing Director. All correspondence is held
in strict confidence.
Rathbun, Sapir & Associates
P.O. Box 2337
Sedona, AZ 86339-2337 * USA *
(520) 203-0074 Office (520) 203-0075 FAX
E-mail: rathbun@sedona.net