Mar 24, 2022
$125,000 - $150,000 yearly
Provide total quality and regulatory management and oversight for all aspects of ABM activities.
Duties and Responsibilities:
Establish clear outcomes and reliable milestones for all regulatory projects executed for and on behalf of ABM.
Responsible for “bullet-proof” regulatory compliance in all aspects of operations, product development and acquisitions.
Oversee the regulatory and quality team members as their activities and responsibilities relate to ongoing regulatory projects.
Attend weekly Executive team, Staff, Regulatory, and Product Development meetings and other meetings as required.
Participates in all aspects of the ABM Executive Team and staff to fully execute tasks to achieve ABM’s mission, goals and objectives.
Ongoing Work Projects:
Fully compliant regulatory systems
USFDA QSR
USFDA CGMPS
ISO 13485
Canadian Medical Device Regulations – Medical Device Single Audit Program
CE Marking from Medical Device Directive
IMCAS...
Aesthetics Biomedical Inc.
Phoenix, AZ, USA
Full time