management system for Act 101 products. Integrate ISO 13485 medical devices into the QMS. Co-audit local audits product review, ongoing stability. GMP auditing/ ISO 13485 auditing experience (advantageous). Experience
management system for Act 101 products. Integrate ISO 13485 medical devices into the QMS. Co-audit local audits product review, ongoing stability. GMP auditing/ ISO 13485 auditing experience (advantageous). Experience
trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) File programs and databases in alignment with ISO 13485 requirements and ensure deadlines are not missed
trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) File programs and databases in alignment with ISO 13485 requirements and ensure deadlines are not missed
/>Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred)
ISO 13485 requirements and ensure deadlines are not missed
File programmes and databases in alignment with ISO 13485 requirements and ensure deadlines are not missed trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred)
File programmes and databases in alignment with ISO 13485 requirements and ensure deadlines are not missed trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred)
applicable to medical device distribution (e.g. ISO 13485). Must have own vehicle.