Pharmaceutical Documentation Expert
4 days ago
Technical Source is a leading provider of pharmaceutical manufacturing solutions. As a Documentation Specialist, you will play a crucial role in ensuring compliance with GMP and regulatory requirements.
Responsibilities:
- Create and maintain accurate documentation related to validation protocols, reports, process changes, and SOPs
- Ensure all documents meet GMP, FDA, and other regulatory standards
- Work closely with validation and process engineering teams to gather and organize technical data
- Perform detailed reviews of documents to identify discrepancies or errors
Requirements:
- 2-4 years of experience in documentation or administrative roles within a pharmaceutical or regulated manufacturing environment
- Bachelor's degree in a relevant field or equivalent experience
- Technical skills: document management systems, Microsoft Office Suite, familiarity with validation processes, engineering documentation, and GMP guidelines
- Exceptional accuracy and focus on detail in reviewing and organizing documentation
Compensation: The estimated salary for this position is $65,000 - $85,000 per year, depending on experience.
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