Tunnell Consulting
Batch Record Reviewer/ Deviations SME (Finance)
The staffing division of Tunnell Consulting, looks for top talent on behalf of our Pharmaceutical/Biotech clients. Currently, one of our client's need a QA Batch Record Review/Deviations SME. This is estimated to be a minimum 3-month project with potential for extension. Onsite is required; location Rockville, MD area. Local candidates preferred.
Title: QA Batch Record Review/Deviations SME
Role:
The QA Batch Record Review/Deviations SME will review batch records for completeness and accuracy as well as assessing any identified manufacturing deviations.
The incumbent will be responsible for conducting and documenting GMP investigations including generation, closing and effectiveness checks of CAPAs for a pharmaceutical manufacturer in their respective areas, including evaluating product impact, conducting the cross functional root cause analysis effort, authoring the investigation and shepherding it for review and approval. Ensure that the investigation process used adheres to the client's policies and SOPs.
Skills:
Tunnell is proud to be an Equal Opportunity / Female / Minority / Disabled / Veteran Employer and does not discriminate on the basis of race, color, religion, sex (including pregnancy, child-birth, or related medical conditions), national origin, ancestry, age, disability, family care status, veteran status, marital status, military status, sexual orientation, gender identity, or any other characteristic protected by law. Tunnell makes reasonable accommodation for persons with disabilities to apply for employment.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.