Global Quality Systems Specialist
Share
Job Location:
Irvine, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Location: Open to remote in US Canada Mexico Brazil Colombia Argentina
The Global Quality Systems Specialist at Advanced Sterilization Products has the responsibility to execute to the global Quality System requirements. This position reports to the leadership of Quality Systems.
Responsibilities
- Manages document revisions ensures compliance with formatting and approval workflows
- Coordinate change control documentation and facilitate cross functional review.
- Analyzes change orders to ensure compliance to GDP requirements and existing procedures.
- Track and monitor quality systems metrics including but not limited to: IE CAPA and NC
- Support timely documentation and closure
- Assist in quality planning activities and QMS review preparation.
- Manage training assignments and monitor training metrics
- Participate in internal audits and support audit readiness activities.
- Support internal audit logistics such as scheduling
- Provide informal guidance to new team members.
- Solves problems in straightforward situations; analyzes possible solutions using technical experience and judgment and precedents
- Explains complex information to others in straightforward situations
- Collaborate with cross-functional teams to resolve issues.
- Collaborate cross functionally to support projects as assigned by direct manager.
- Responsible for communicating business related issues or opportunities to next management level.
- Supports continuous improvement initiatives
- Perform other duties as assigned.
Qualifications
- Working knowledge of quality management systems and experience with ISO 13485.
- Excellent written and verbal communication skills (English)
- Demonstrated ability to train mentor and coordinate the work of others in daily operations
- Seeks to deeply understand customer needs and prioritize work accordingly
- Willing to take on the unknown and overcome adversity to support the goals of the business
- Seeks varied perspectives and experiments with new ways of solving problems
- Collaborates in support on teams success
- Demonstrates urgency and ownership to consistently deliver on objectives using FBS
Experience and Education
- Bachelors degree in engineering science or related field.
- Minimum 3 years of experience in a quality or regulatory role in medical devices or related regulated industry.
- Equivalent combination of education and experience will be considered.
Required Experience:
IC
Key Skills
- Quality Assurance
- FDA Regulations
- Data Collection
- Food Safety Experience
- ISO 9001
- Mobile Devices
- Root cause Analysis
- Quality Systems
- OSHA
- Food Processing
- Quality Management
- cGMP
About Company
Fortive Corporation Overview Fortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product d ... View more
