consistently deliver to quality, time and cost standards
consistently deliver to quality, time and cost standards
consistently deliver to quality, time and cost standards
Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs actions. Document Control Reviewing and updating of Standard Operating Procedures and Quality Documents. General
Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs actions. Document Control Reviewing and updating of Standard Operating Procedures and Quality Documents. General
Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred)
Experience with Regulatory Affairs
/>Document Control
Reviewing and updating of Standard Operating Procedures and Quality Documents.
safety of oneself and others. Adhere to ethical standards and regulations governing laboratory research
safety of oneself and others. Adhere to ethical standards and regulations governing laboratory research
close contact with the study management group and consult them on strategic issues that might have any safety clinical study in accordance with GCP regulations and standard operating procedures
Patient care
close contact with the study management group and consult them on strategic issues that might have any safety clinical study in accordance with GCP regulations and standard operating procedures Patient care and screening