Document Control Specialist - Quality
Tandym Group · Bedford, MA · 3 days ago
Quality AssuranceFull-time
About the role
A biotech organization located in Bedford, MA is seeking a Document Control Specialist, Quality.
Responsibilities
- 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
Qualifications
- 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
Desired Skills
- Experience documenting processes and supporting continuous improvement efforts
- Exposure to audit and inspection support in a regulated environment