The Manager will handle site-level Quality System compliance, ensuring full compliance of the site quality System with US FDA, ISO 13485, MDSAP/MDR and other applicable country specific regulatory requirements. Specific focus will be on QC testing, documentation review, and product release. 

Responsibilities:

• Establishes, maintains, and promotes a strategy for compliance with quality objectives.
• Ensure product is tested in accordance with company policies and procedures.
• Ensure product release is conducted in accordance with company policies and procedures.  Ensures product is not released for distribution until all Device Master Record requirements have been met.
• Ensures timely and accurate evaluations and investigations. Implements prompt actions as necessary to ensure product safety and efficacy based upon investigation results.
• Manages and ensures follow-up on activities related to Internal and External QMS Audits.
• Establishes, maintains, and promotes a culture of compliance/regulatory requirements and a keen focus on quality and customer requirements throughout the site organization.
• Establishes and maintains a robust employee training process.
• Manage direct reports to ensure timely completion of activities to support release of products.
• Establish and maintain an effective and compliant site Document Control process.
• Approve / Sign-off work of direct reports and other team members.
• Identify process improvement opportunities to enhance surveillance and to increase efficiency.
• Participate in and lead cross-function and cross-location activities to improve efficiency and compliance.
   

Requirements:

• Bachelor's degree (preferably science or engineering discipline) required.
• At least 7 or more years of experience in Medical Device Quality Operations.
• Broad extensive knowledge of methods, processes, equipment, and techniques in manufacturing, development, and engineering.
• Significant knowledge and experience with designing and implementing QMS processes that meet the requirements of ISO 13485, 21 CFR 820, and MDR.

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

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