(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...
, test methods, work instructions, and reports in a cGMP or QSR setting Proven ability to interview SMEs, translate complex...
related to the proper receipt, quarantine, storage, and disbursement of materials as it relates to FDA, OSHA, QSR, ISO, Good...
for assembly, packaging, and prep operations in compliance with approved documentation and QSR, including: Line clearance...
, storage, and disbursement of materials as it relates to FDA, OSHA, QSR, ISO, Good Manufacturing Practices and other Roche...
compliance with ISO, QSR, FDA regulations, and company manufacturing policies Maintain accurate documentation for quality...: Medical device manufacturing experience Familiarity with ISO, QSR, FDA regulations, Lean manufacturing, GMP, or cleanroom...
, OSHA, QSR, ISO, Good Manufacturing Practices and other firm policies and procedures. Ability to recognize minor issues...
industries such as medical device, diagnostics, or pharmaceuticals. Knowledge of regulatory frameworks such as QSR and ISO...
relates to FDA, OSHA, QSR, ISO, Good Manufacturing Practices and other Roche policies and procedures. â—¦ Recognizes minor...
to the proper receipt, quarantine, storage, and disbursement of materials as it relates to FDA, OSHA, QSR, ISO, Good...