Job Opportunity
This position involves overseeing quality assurance in various operational areas of a pharmaceutical site. The ideal candidate will possess relevant experience and knowledge of quality systems, regulations, and industry standards.
Main Responsibilities:
* Monitor and support quality operations in manufacturing, testing, packaging, and material management
* Review and approve critical documents such as batch records, cleaning records, and other quality reports
* Participate in regular meetings, internal audits, and quality assessments to ensure compliance
* Drive improvement initiatives using Lean methodology to enhance process efficiency
Requirements:
* Bachelor's degree in a relevant scientific field
* Advanced degree preferred but not required
* Minimum 5 years of experience in the pharmaceutical industry with current knowledge of cGMPs and regulatory guidelines
* Significant experience in equipment qualification, cleaning validation, and process validation is highly desirable