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Smithers Pharmaceutical Development Services (PDS) business is a specialized bioanalytical contract research organization (CRO) that supports the development of biologics and vaccines from discovery through phase 4 with expertise including bioassays and high sensitivity assays and gene therapy. PDSs services focus primarily on development validation and sample analysis for PK/TK ADA and biomarker and translational sciences assays.
We have a great opportunity available for a parttime summer intern within our Quality Control Document Review team. This opportunity will provide the selected intern with an opportunity to be introduced to some of the work necessary in ensuring compliance with FDA requirements for GLP regulated studies in various stages of the FDAs drug approval process. The selected intern will receive training and work with our QC team to review documents generated by different laboratory groups for any findings (errors omissions SOP deviations etc.) that need to be addressed.
Expected duration: (May 27th/June 9th through August 22nd/August 29th)
Hours/week: 16 to 24
Candidate must be a minimum of 18 years of age.
Must have a HS Diploma or GED.
Must have strong attention to detail.
Have an interest in pursuing a career or advanced education in a scientific field or support role within a scientific company.
The rate of pay is minimum wage for Montgomery County MD currently $17.15 per hour.
Required Experience:
Intern
Part-Time