Document Control Specialist - Quality
Tandym Group
A biotech company in California is looking to add a new Document Control Specialist, Quality to support document management operations within a quality environment. This role focuses on processing and maintaining GxP documents throughout their lifecycle, with an emphasis on controlled issuance, reconciliation, and archival.
About the Opportunity:- Schedule: Monday to Friday
- Setting: Onsite
- Follow the Standard Operating Procedures (SOPs), work Instructions, and other administrative practices
- Organize and manage a high volume of documentation for electronic and paper-based archival
- Assist with filing, retrieval, retention, and archival of documents and records
- Support the issuance of controlled documents and related document reconciliation activities
- Provide Document Control support before, during, and after audits and inspections
- 1-4 years of Quality experience in the Pharma, Biotech, or related Life Sciences industry
- Bachelor's Degree in Science, Engineering, or related discipline
- Experience in Document Control and Electronic Document Management systems
- Strong attention to detail and organizational skills
- Ability to work independently, prioritize tasks, and manage multiple assignments simultaneously.
- Knowledge of GDP and cGMP principles
- Proficiency in Microsoft Excel, Word, and PowerPoint
- High ethical standards, good judgment, and professionalism
- Experience documenting processes and supporting continuous improvement efforts
- Exposure to audit and inspection support in a regulated environment
Vacancy posted 20 hours ago
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