Quality Supervisor

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world’s top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

Jabil Inc.

Quality Supervisor

Job Description: 

Quality Supervisor positions offered by Jabil Inc. (St. Petersburg, FL). Supervise the Management Controls and Document Control within the Corporate Healthcare customer division. Responsible for the execution of monthly, corporate site and business unit (15 sites) quality reviews. Provide guidance and support to cross functional team at manufacturing sites, establishing a streamline process to be use across the network. Mentor junior engineers in the document control process and quality systems management. Execute analysis and provide solutions to meet customer agreements and specifications. Translate customer and business needs into quality process operations and business services. Support the Quality Management System go-live activities of multi-site and cross-functional teams within the organization. Participate in development and execution of Quality Plans to launch the Jabil Healthcare Quality Systems at the customer location sites. Collaborate in the development and execution of improvement plans to recover site metrics. Execute corporate nonconformances and CAPA investigations. Support Jabil’s HC customer facing activities and workshops preparation. Responsible for Risk Assessment for Jabil Healthcare Corporate site as per Medical devices and application of risk management to medical devices ISO 14971:2019.

Minimum Requirements: 

Requires a bachelor’s or foreign equivalent degree in Engineering, Bioscience, or a related field and 2 years of experience in the position offered or 2 years of experience developing quality management systems for medical device manufacturing. Also requires 2 years of experience: applying Risk Management ISO 14971 principles; facilitating workshops with strategic customers to address quality concerns; serving as business process owner for quality action systems for NR, CAPA, audit, and customer communications; developing quality system management review presentations on KPI and quality system effectiveness including resource and risk management for senior leadership; and ensuring corrective action plans are effectively implemented to meet defined effectiveness criteria. Position reports to office in St. Petersburg, FL but may telecommute from any location in the U.S. Experience may be, but need not be, acquired concurrently.

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Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

Accessibility Accommodation

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to [email protected] or calling 727-803-7988 with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong#AWorldofPossibilities