(Contract) Technical Writer
, test methods, work instructions, and reports in a cGMP or QSR setting Proven ability to interview SMEs, translate complex...
, test methods, work instructions, and reports in a cGMP or QSR setting Proven ability to interview SMEs, translate complex...
environment Solid understanding of FDA QSR, ISO 13485, and GMP requirements Process & Validation Expertise Hands...
continuous improvement initiatives and ensure all processes comply with ISO, QSR, and FDA regulations. Work Schedule: Monday...