Quality Assurance Associate, Records Management

Ocular Therapeutix

Bedford, MA, United States
Base: $76,000 - $83,000 usd; bonus/equity: not spe...
On-site
Electronic document management system administration
Gxp environment experience
Controlled document issuance and archival
Ocular Therapeutix is seeking a Quality Assurance Associate for their Records Management team in Bedford, MA. The role involves overseeing document management processes, ensuring compliance with regulations, and supporting training initiatives within the eDMS system

Job Summary

  • The role supports all activities within the Records Management team including administering the electronic Document Management System and supporting the document revision process.
  • Candidates must maintain appropriate filing structures to keep archived material identified, secure, and easily retrievable while ensuring chain of custody for controlled documents.
  • Ocular Therapeutix strives to build a strong culture where employees can flourish through out of the box thinking and cross-functional collaboration.

Matching Summary

Match Score: 85

Ocular Therapeutix is seeking a Quality Assurance Associate for their Records Management team in Bedford, MA. The role involves overseeing document management processes, ensuring compliance with regulations, and supporting training initiatives within the eDMS system.

Salary

Base: $76,000 - $83,000 USD; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Electronic Document Management System administration
  • GxP environment experience
  • Controlled document issuance and archival
  • MasterControl system proficiency
  • Quality documentation processing

Nice-to-have

  • Cross-functional collaboration skills
  • Process improvement initiative participation
  • Technical writing capabilities
  • Out of the box thinking
  • Customer focus communication

Key Requirements

  • Associate's degree or equivalent required
  • Minimum 3 years document management in GxP environment
  • Minimum 5 years working in GMP environment preferred
  • Proficiency with MS Office suite
  • Experience with MasterControl or similar eDMS

Work Rights

Not specified

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