Our client has over 50 years of experience and expertise, provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services.
Job Title: Document Review Specialist (Contract)
Location: Vista, CA (Onsite)
Pay: $30/hr-32/hr
Duration: 3 months with potential for extension
Position Overview:
We are seeking a meticulous and organized Document Review Specialist (Temp) to support our clients Quality, Regulatory, or Technical Operations teams. The successful candidate will review technical documents, track approval workflows, and extract data from executed records to support compliance and operational excellence.
Key Responsibilities:
- Review scientific and technical documents for accuracy, completeness, and compliance with internal quality standards and regulatory requirements.
- Monitor and manage document approval workflows, ensuring timely reviews and finalizations across cross-functional teams.
- Edit, format, and prepare documentation including SOPs, protocols, reports, and related materials.
- Extract and organize data from executed documents to support tracking, reporting, and audits.
- Collaborate with internal teams (e.g., Quality Assurance, Regulatory, Manufacturing) to streamline documentation processes and resolve discrepancies.
- Maintain compliance with Good Manufacturing Practices (GMP) and company policies in all documentation activities.
Qualifications:
- 1-3 years of experience in document-related roles (e.g., document control, technical writing, quality documentation).
- Familiarity with reviewing or interpreting scientific and technical content.
- Strong attention to detail and a commitment to accuracy.
- Excellent written and verbal communication skills.
- Experience with document tracking systems or workflow tools.
- Working knowledge of GMP regulations and documentation best practices.
- Proficiency in Microsoft Office Suite, particularly Word and Excel; experience with document management systems (e.g., Veeva, MasterControl) is a plus.