Summary from listing
The QA Compliance Officer Process - Document Coordinator will manage and coordinate documentation for aseptic product projects, including new NCE or NBE products and combination products. The role oversees GMP documentation lifecycle, local procedures, alignment with training systems, document management and training information systems, and continuous improvement. It requires a relevant university degree, more than five years of pharmaceutical quality-systems experience, knowledge of document management and training systems, and fluency in English and Spanish. Benefits include flexible working hours, life and accident insurance, medical insurance, training and development, health care, and smartworking.
