I am looking for a Scientist to work in Quality Assurance. This person will
develop and validate analytical methods related to NDA commitments and foreign
registry requirements for its products. The candidate will be responsible for
providing guidance and leadership to QC analysts in method improvement,
enhancement and transfer; managing cross validation of analytical methods;
preparing reports and maintaining laboratory notebooks according to cGMP's and
established SOP's; and supervising QC analysts. The position requires a Ph.D.
with 1-4 years experience in the pharmaceutical industry or an MS with a
minimum of 6 years in the pharmaceutical industry. Candidates must have
knowledge of cGMP's and strong background in all analytical techniques;
chromatography experience is needed. We are a leading biotech firm with
research facilities in Baltimore, Maryland and can provide excellent benefits
(health insurance, dental, and vision plan, stock options, bonus program, paid
vacation and more). A high impact, high profile position with excellent
opportunity for advancement. Please contact Scott Shanes by phone at
609-584-8733 Ext. 218, fax CV and cover letter to 609-584-9575 or E-Mail to
sis at dmc10.comsis@diedremoire.com
