
Quality Assurance Consultant
3 days ago
Target start date: Monday June 26th
Duration: 6 months.
Work schedule: 5 days week on site. 8:30am-5pm
Client Domain: Biotech client, manufacturer of the covid vaccinee
Visa: All except H1
Rate: $55-58/hr C2C
Quality Documentation Control Reviewer
Project description:
Our client has 26,000 records that need to be assessed and mitigated. These documents have been already diverted into mitigation buckets and are already in Veeva Vault. A risk migration plan has already been created. The qualified individual will need to assess where these documents fall and into which bucket. With this gap the team has identified that they will need to add five highly qualified document reviewers to their growing team who have prior documentation review experience and who have good documentation practice experience as well.
Technology environment the consultant will be working in:
This individual will be required to have experience with Veeva Vault and other applicable QMS
systems.
Consultants' day to day 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:
• 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
• Veeva Vault
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