Sr Manufacturing Support Coordinator

Johnson & Johnson • Jacksonville, FL

5d • Onsite

About The Position

Johnson & Johnson Vision is recruiting for a Senior Manufacturing Support Coordinator, located in Jacksonville, FL. About Vision Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Role Summary The Senior Manufacturing Support Coordinator will support manufacturing operations by maintaining key production metrics, monitoring back orders, supporting product flow, and partnering with cross-functional teams to resolve production and quality-related issues. This role will also support non-conformance activities, CAPA investigations, and product disposition processes in accordance with established procedures and regulatory requirements.

Requirements

• An Associate degree, Vocational Technology Certificate, Trade School certification, military training, or equivalent experience is required.
• A minimum of six (6) years of professional business experience is required.
• Prior medical device manufacturing experience is required.
• Ability to demonstrate positive impact across multiple areas of the business is required.
• Ability to identify and describe examples of manufacturing process variation is required.
• Basic statistics experience is required.
• Understanding of compliance and regulatory requirements is required.
• Strong communication, organization, and follow-up skills are required.

Nice To Haves

• Experience working in a regulated manufacturing environment is preferred.
• Prior leadership experience is preferred.
• Experience pulling and analyzing production data is preferred.
• Knowledge of quality systems, non-conformance processes, CAPA, and documentation practices is preferred.

Responsibilities

• Coordinate, drive, and maintain weekly plant OPP and WIP metrics.
• Monitor department back orders and assist with expediting product to support business needs.
• Identify, investigate, and help resolve aging WIP by partnering with appropriate cross-functional teams.
• Lead department Corrective Information investigations related to non-conformance events.
• Monitor department quality events and provide non-conformance updates during daily and monthly review meetings.
• Support CAPA investigations and partner with Quality, Operations, Engineering, and other functional teams as needed.
• Coordinate product return, release, quarantine, disposition, and destruction activities in accordance with established procedures.
• Support department initiatives, special projects, and continuous improvement activities as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Associate degree