Sr. Quality Program Manager

Job Posting Start Date 05-13-2024 Job Posting End Date 07-22-2024

Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.

We believe in the power of diversity and inclusion and cultivate a workplace culture of belonging that views uniqueness as a competitive edge and builds a community that enables our people to push the limits of innovation to make great products that create value and improve people's lives.

A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.

Job Summary

To support our extraordinary teams who build great products and contribute to our growth, we’re looking to add a Requalify Program Manager located in Austin, TX

Reporting to the Director of Quality the Sr. Quality Program Manager role will be in-charge of guiding a team of cross functional experts in the delivery of customer focused products and services and will hold up development and implementation of a project, pricing and program strategies in order to continue to deliver value to the business and its customers

What a typical day looks like:

• Responsible for internal tracking system for deviations / non-conformances, including issuance, review and approval of corrective and preventive action systems.
• Responsible for ensuring investigations are robust and that corrections and/or corrective actions taken eliminate the non-conformance.
• Responsible for the maintenance of the Quality Management System (QMS) and associated documents
• Lead compliance and process improvement initiatives related to the Quality Management System.
• Supports QMS Management Reviews, Quality Updates, etc.
• Assist in the preparation, coordination, and execution of Compliance (ISO) and Regulatory (FDA) audits
• Establish and maintain successful cross-functional relations with Engineering, Manufacturing, IT, and Quality departments. Coordinate corrective actions for issuance, review, and closure of action plans.
• Engage with customer, present data / presentations, follow up to ensure resolution on issues
• Ensure that document release packages are accurate, complete, and current and that all documents are maintained and controlled.
• Assist in other quality systems responsibilities requested by management to ensure a robust and compliant Quality Management System. 
• Develop and implement performance metrics.

The experience we’re looking to add to our team:

• 10 years of experience in program administration/ management or related area. 
• 10 years of Medical Devices (FDA CFR 820, ISO 13485) experience
• Training experience
• Experience in Contract Manufacturing and international regulatory requirements preferred

What you’ll receive for the great work you provide:

• Full range of medical benefits, dental, vision
• Life Insurance
• Matching 401K
• PTO
• Tuition Reimbursement
• Employee discounts at local retailers

Job Category

Operations

Is Sponsorship Available?

No

Flex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We celebrate diversity and do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).