Employment Opportunities
PharmAthene, Inc. is experiencing an exciting period
of development and growth. These events have brought
about the need to add additional positions to the
organization. PharmAthene is currently searching
for qualified candidates for the position(s) noted
below. Should you wish to be considered for a certain
position, please e-mail your resume (in Word format)
with salary requirements to hr@pharmathene.com and
note the position title and number in the “subject”
line of the e-mail.
As PharmAthene’s operations are focused in biodefense,
which is subject to special restrictions under
International Traffic in Arms Regulations,
U.S. Citizenship or U.S. Permanent Resident status may
be required. PharmAthene offers a challenging, dynamic
environment with growth opportunity, competitive
compensation and a full benefits program. Only those
candidates meeting the requirements noted below and
selected for an interview will be contacted.
PharmAthene provides equal employment opportunities (EEO)
to employees and applicants for employment in accordance
with applicable federal, state and local laws.
Manufacturing Sciences/Engineer (08-007)
The Manufacturing Sciences/Engineer will provide
hands-on technical directions for all aspects of
the manufacturing of biologics, including technology
transfer, process validation, and process troubleshooting.
The individual will monitor process performance at the
contract manufacturing organization (CMO) and ensure
successful delivery of products with regard to time, quality
and cost.
Responsibilities/Duties: Technology and process assessment
of upstream and downstream processes at the CMO, preparation
of appropriate CMC sections for IND, NDA and BLA submissions.
Requirements include:
- Advanced Degree in pertinent area (chemical engineering, chemistry, biology, biotechnology, pharmaceutical sciences, etc.)
- At least 10 years or more experience in biologic (cell culture highly desired) development and manufacturing.
- An equivalent combination of education and experience with a demonstrated track record in new product development will also be considered.
- Experience should include writing of CMC sections for regulatory submissions, thorough understanding of GMP and hands-on process development experience with recombinant proteins.
- Strict attention to detail, excellent communication skills - both written and oral, strong interpersonal skills, self-motivated with a strong work ethic, good time/priority management skills, and able to work independently and/or in a team environment.
Last Updated: 08/14/08
