Currently I have an opening for a QC Specialist located in Lexington, MA. Details for the position are as follows :

Job Description :

• Primary duties of the position are focused on non-laboratory support of the QC functions.
• Primary activities would generally include but not limited to analytical method transfer, analytical method validation, data analysis, data trending, project and testing coordination product and material specification management, inspection support, document authoring, revisions, initiating / completing quality systems, method / equipment validation and method projects activities.
• Contributes to the completion of organizational projects and goals. Errors in judgment or failure to achieve results would normally require a moderate expenditure of resources to rectify.
• 50-60% data analysis, data trending, project and testing coordination, support of product specification management, COA generation, material specification creation, document revisions.
• 20-30% Regulatory and / or inspection support, method projects activities, initiating / completing quality systems.
• 20% Involvement in other QC activities as required (ex. records retention).
• Software skills : MS Office, LIMS, SAP, Trackwise, EDMS, and QMS compliance.
• Bachelors 5 years or master’s with 3 years of GMP / cGMP experience and skills in method development, method transfer, method validation, and any bioassays, capillary electrophoresis, or HPLC.

Technical Information :

• Pay : $50-62 hourly, depending on experience level
• 6-month contract with potential for extension or conversion to permanent
• Onsite, M-F, 8am-5pm
2 days ago