Quality Assurance Document Supervisor- Manufacturing Industry

Job Id OOJ - 19838
Job Title Quality Assurance Document Supervisor
Industry(ies) Biotechnology/ Life Sciences,Pharmaceutical
Primary Skills Quality Assurance Professionals
Location -Lancaster, SC
Work Experience (Years) 3-15
Degree University - Bachelor's Degree/3-4 Year Degree
Pay Rate ********
Job Description
Initiating investigations, assessing NCRs to determine if they have the necessary information to be closed out. Oversee the Finished Product Update spreadsheets, including downloading the recently packaged batches from SAP and ensuring the laboratory sample receipt dates are accurate. Track individual reviewer metrics to determine if additional training or guidance is needed. Ensure cross training is performed and documented for individuals within the QA Document Specialist group. Establish and oversee an organized system for both buildings to meet turn-around time goals. Establish and oversee an organized system to track the change control process. Hold monthly team meetings to ensure both buildings are communicating and working together as a team. Perform other assigned duties as may be required in meeting company objectives Regular attendance is required. Communicate effectively with other departments within the organization and function within a team environment. Qualifications
Bachelors or Associates degree with 5 years' experience in a cGMP environment
Must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control.