Biotech Document Reviewer

4 days ago


Norwood, Massachusetts, United States Saxon Global Full time
Job Description:
Saxon Global is a leading provider of quality assurance services. We are currently seeking a Biotech Document Reviewer to join our team in Norwood, MA.

About the Position:
This is an excellent opportunity to work with a biotech client, manufacturer of the Covid vaccine, on a six-month project. Your responsibilities will include reviewing multiple documents daily, converting them into the QMS system, and transitioning paper-based and electronic documents to Veeva Vault.

Key Responsibilities:
- Responsible for quality documentation review
- Reviewing multiple documents daily and being able to convert the documents into the qms system
- Documents will consist of paper-based and electronic-based documents that need to be transitioned to Veeva Vault

Required Skills and Qualifications:
- Must have at minimal two plus years of quality documentation review experience
- Must have Good Documentation Practices (GDP) experience
- Must have experience with risk assessments
- Must have One year of quality review experience

Benefits:
The successful candidate will receive a competitive salary, commensurate with their experience, as well as opportunities for professional growth and development.

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