Quality Assurance Consultant

3 days ago


Norwood, Massachusetts, United States Saxon Global Full time
Location: Norwood MA

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

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