Precigen · 19 hours ago
Document Control Specialist
Germantown, MD
Full-time
Onsite
Senior Level
5+ years expPrecigen is a company focused on Quality Assurance, and they are seeking a Document Control Specialist to manage the daily operations of controlled documents and records. The role involves executing the document control process, maintaining documents, and supporting overall QA functions.
BiotechnologyLife ScienceMedicalTherapeutics
Responsibilities
Execute the daily functions of the document control process including but not limited to: formatting documents, tracking documents through the review/approval cycle, issuing documents for execution, reconciliation of issued records, and archiving
Scan, organize, maintain, and file documents, adhering to the company's document lifecycle procedures. Includes both paper-based and electronic filing
Issue labels for finished products and Quality Control samples
Support overall QA functions; perform additional duties as assigned by supervisor
Qualification
Required
High School diploma, Associate or Bachelor's Degree or commensurate experience
Minimum five (5) years of experience in a regulated work environment
Experience with document control systems; experience with Veeva is a plus
Experience working within a GxP pharma/biologic environment is a plus
Strong understanding and use of Microsoft Office Suite and Adobe Acrobat Pro
Preferred
Experience with Veeva is a plus
Experience working within a GxP pharma/biologic environment is a plus
Company
Precigen
Precigen is a life sciences company researching and developing bio-therapeutic control systems to minimize toxicity.
51-200 employees
Funding
Current Stage
Public CompanyTotal Funding
$809.8MKey Investors
Pharmakon AdvisorsPatient Capital ManagementThird Security
2025-09-02Post Ipo Debt· $100M
2024-12-27Post Ipo Equity· $79M
2024-08-06Post Ipo Equity· $30M
Leadership Team
Rutul R. Shah
Chief Operating Officer
Bryan T. Butman
Senior Vice President and Head of CMC
Recent News
Company data provided by crunchbase