Supervisor Qa Product Release

Details of the offer

The Company Dexcom Corporation (NASDAQ DXCM; Market Cap $44.3B) is a pioneer and global leader in continuous glucose monitoring (CGM).
Dexcom began as a small company with a big dream: To forever change how diabetes is managed.
To unlock information and insights that drive better health outcomes.
Here we are 25 years later, having pioneered an industry.
And we're just getting started.
We are broadening our vision beyond diabetes to empower people to take control of health.
That means personalized, actionable insights aimed at solving important health challenges.
To continue what we've started: Improving human health.We are driven by nearly 10, ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable.
We've already changed millions of lives and we're ready to change millions more.
Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions.
We'll get there by constantly reinventing unique biosensing-technology experiences.
Though we've come a long way from our small company days, our dreams are bigger than ever.
The opportunity to improve health on a global scale stands before us.SummaryPerforms supervisory and administrative duties associated with inspection personnel management.Coordinates the tasks and work plans of the product release inspections.Ensure that all quality control activities comply with applicable regulatory requirements.Essential Duties and ResponsibilitiesLead a team of quality inspectors to perform thorough inspections of final products before shipmentImplement and manage in-process quality control procedures to monitor and evaluate production processesCollaborate with production teams to identify and address quality issues in real timeSupport in routine audit readiness activities including cconduct regular Gemba walk, inspections and audits to ensure compliance with quality standardsMaintain accurate and detailed records of in-process and outgoing quality control activitiesPrepare and submit comprehensive quality reports to management, highlighting key performance indicators, trends, and areas for improvementParticipate in root cause analysis and corrective action initiativesProvide training to production and quality control personnel on quality standards, procedures, and best practicesFoster a culture of continuous improvement and quality consciousness throughout the organizationStay updated on relevant industry regulations and standardsWorks with QA, Manufacturing, Engineering, Supply chain and other department personnel, as necessary, to support quality and business objectivesAssumes and performs other duties as assignedRequired QualificationsMinimum a Bachelor's degree with = 3 years of medical device, pharmaceutical, or other regulated industry experienceStrong understanding of quality management systems, regulations, and standards (e.g., ISO )Experience with statistical tools and methods for quality controlProficiency with Microsoft Office, ERP SystemStrong problem solving and data analysis skillExcellent leadership and communication skillsAbility to work collaboratively across cross-functional teamsAbility to work hands-on in a fast-paced environmentDetail-oriented with a focus on continuous improvement


Nominal Salary: To be agreed

Source: Talent_Ppc

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