Quality Supervisor- DC- Phoenix, AZ

COMPANY DESCRIPTION At AirLife, we are dedicated to improving the quality of every breath.
Excellence with Every Breath is not just a tag line, but the way we work and take care of our customers.
With a mindset to evolve, innovate, and grow, we are a premier manufacturer of the highest-quality and market-leading breathing consumables.
This growth philosophy has positioned us to increase our global footprint and business reach, impacting even more people around the world.
Our expanding family of the most trusted brands offers a product portfolio that spans the continuum of care from first responder to home care, with safety, patient comfort, and clinical performance in mind.
Collective expertise allows us to provide quality products and experiences to our patients, customers, and our people.
Our values of Customer first, Differentiate with our People, Bias for Action, Continuous Improvement and Accountability define who we are and how we work.
Join us! POSITION SUMMARY Quality Supervisor will be responsible for Quality operations occurring at the Phoenix, AZ Distribution Center, including the overall Quality of product through the facility.
This position ensures products are meeting internal, customer, and regulatory requirements, and that processes and transactions are being conducted in an efficient, compliant manner.
As Quality Supervisor, this role is expected to work collaboratively in a cross-functional team, and will be responsible for overseeing the Quality Control and Inspection teams operating at this facility, ensuring they have the support, tools, and processes in place to conduct their responsibilities as expected.
The Quality Supervisor is expected to drive a strong focus on team development, engagement, and professional growth.
As a leader within the Quality department, this position will participate in strategic initiatives including inventory and process flow planning, continuous improvement activities, and focus on customer and patient safety.
POSITION QUALIFICATIONS The specific minimum competencies needed to perform the essential duties of the job include knowledge, skills, abilities, level of education, and experience necessary for successful performance.
These competencies are generally demonstrated through specific service, education, or training.
Knowledge: Knowledge of quality standards for medical devices (e.
g.
, ISO 13485, FDA QSR, MDSAP, EU Medical Directives, and Canadian Medical Device Regulations.
Skills & Abilities: Excellent verbal and written communication skills.
Excellent organization skills and attention to detail.
Ability to multi-task.
Sound, systematic problem-solving skills.
Strong computer skills: MS Word, MS Excel, PowerPoint, Database Management and Statistical Analysis.
Level of Experience: A minimum of 5 years of Quality System experience in an FDA regulated and/or ISO certified facility (preferably ISO 13485).
A minimum of 3 years in a leadership role, leading and mentoring employees A minimum of 3 years in quality control and product inspection Experience in a warehouse or distribution center a plus Level of Education: Bachelor/Associate degree or equivalent work experience.
Travel: Occasional overnight travel (up to 5%).
ESSENTIAL DUTIES AND RESPONSIBILITIES The core tasks, duties, and responsibilities that must be performed on the job.
Support team through sort and rework activities, and ensure adequate resources for completing daily and project-based work punctually.
Represents customer requirements internally.
Communicates with outside departments within the plant and in other company facilities to ensure a continuous operational flow.
Communicates cross-functionally concerning quality and testing issues.
Lead a team of 1-4 quality control specialists focused on product quality and compliance.
Provide oversight of activities in the Quality inspection laboratory, and management of all equipment therein.
Investigates operational and technical issues, leading root cause and troubleshooting activities, resolution of problems, and thoroughly documented activities.
Owner and leader of nonconformances and CAPAs as it relates to acceptance criteria and distribution processes.
Ensures compliance to AirLife SOP's and quality control documents for product and manufacturing within the warehouse and distribution centers.
Utilizes data to drive quality control results.
Reports to upper management on the performance of product quality and any need for improvement Support pre-audit and post audit activities and facilitate closure of audit findings impacting relevant facilities and processes.
Create, identify, and report on quality metrics when necessary.
Identify areas of opportunity and support continual improvement of the Quality Management System.
Communicates with all departments to ensure a continuous operational flow.
OTHER RESPONSIBILITIES Focus on achieving our Company mission.
Demonstrate accuracy and thoroughness in daily work; look for ways to improve and promote quality & safety.
Inspire the trust of others; treat people with respect and dignity and embrace the value of diversity.
Use time efficiently; perform job accurately, thoroughly, and conserve Company resources to improve profits.
Contribute to building and maintaining a positive team environment.
Assure all policies and guidelines are implemented and followed.
QUALITY POLICY At AirLife, Quality is our promise.
It is our commitment to customer satisfaction and our dedication to product excellence in an evolving global healthcare market.
This promise is kept through a continuously improving and effective Quality Management System and compliance to Regulatory Requirements.
DEIA STATEMENT At AirLife, we are committed to building a diverse workforce and an inclusive workplace that reflects the communities and customers we serve.
We believe our philosophy on Diversity, Equity, Inclusion, and Advancement (DEIA) encourages excellence and equips us to serve an evolving global marketplace.