Duties:
Perform dose formulation analysis under FDA GLPs for nonclinical studies.
Provide dose formulation stability testing for GLP studies.
Develop and validated analytical methods for doser formulation analysis.
Assume responsibility for analytical support of nonclinical studies as contributing scientist/principal investigator working with BI nonclinical drug safety study directors and CRO scientists/study directors.
Review laboratory notebooks and chromatographic data.
Write analytical reports for inclusion in nonclinical study reports.
Write dose formulation stability reports for GLP study support.
Skills:
Expertise in HPLC and analytical method development. Preferred experience in GLPs, Microsoft Office, Empower chromatographic data system.
Education:
Bachelor’s Degree and 7-10 years’ experience in analytical chemistry/chromatography
Richha Saini
Senior Clinical/Pharmaceutical Recruiter
Tel: (201) 524 9600 Ext 7179
Direct: 781-262-3067
Job details are sourced from the employer's original posting.
Open job postingAbout the company
USTECH is a global firm providing a wide-range of talent on-demand and total workforce solutions. Through the USTECH Talent Network of 100% company-owned and managed offices, we provide highly-skilled professionals whose education, skills and experience are vetted and matched to your unique hiring needs, work environment and company requirements. Our 24x7 global service delivery drives time and cost out of any recruiting and staffing process (15-30% cost reduction in most cases) across all of our services and solutions, providing you with the talent you need on-demand when, where and how you need it.