Quality Control Associate II

Position Details: 

Client Direct Client

Location Research Triangle Park, NC

Job Title Quality Control Associate II

Duration 1 Year+

Must have skill-set [Job Description] Primary Responsibilities 

The primary responsibilities for a Quality Control Associate II include: 

• The execution of QC routine testing to include TOC, conductivity, and nitrates. 

• In addition, the Associate II will be responsible for executing TOC method validations and all associated activities. 

• All activities are executed in a cGMP manner. 

• Additional responsibilities include, but are not limited to, data review/analysis, analytical/technical support and problem solving capabilities, technical writing skills, support of method transfer, execution of robust and compliant cGMP documentation practices, and an understanding of FDA/EMEA regulations. 

• An Associate II will adhere to the Quality Systems and apply them, as appropriate, to daily functions. 

• The Associate II will proactively communicate with direct management regarding cGMP compliance and identification of issues and/or corrective actions on the laboratory floor. 

• The Associate II will be able to work effectively within the group to promote robust teamwork by having both verbal and written communication skills. 

• The Quality Control Associate II will possess demonstrated technical ability regarding fundamental laboratory techniques, analytical methodology, and method validation. 

• The position requires but is not limited to the following: Understanding of basic biological science principles; ability to communicate with peers and management; effective organizational skills; ability to multi-task and coordinate multiple activities in parallel; developing or demonstrated instrument/method troubleshooting and problem solving skills; general knowledge of FDA/EMEA regulations and compliance.