Manufacturing Supervisor

Johnson & Johnson•Jacksonville, FL

17h•Onsite

About The Position

Johnson & Johnson is recruiting a Manufacturing Supervisor to join its diverse Vision Care team located in its Global Headquarters 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 Purpose: This position provides leadership and supervision to the department shifts for production performance regarding safety, quality, cost, and conformance to schedule. Primary responsibilities include supervising, developing, and providing directions to assigned manufacturing staff, and technical and leadership support for the Manufacturing Manager. Supervises the adherence to safety, environmental, quality, and regulatory policies & procedures.

Requirements

Vocational/Technical certificate or associate degree required or equivalent experience.
2-4 years’ manufacturing experience
2+ years of supervision experience
Excellent written and oral communication skills.
Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
Stooping, Crouching, Walking, Pulling, Light Lifting (Up to 25 lbs.), Grasping, Hearing, Visual Acuity, Reaching, Pushing, Talking, Standing, Inside Environmental Conditions, Other
Ability to work rotating 12-hour shifts, 6pm to 6am or 6am to 6pm, including weekends, on a regular basis required.

Nice To Haves

Bachelor's degree or equivalent experience preferred – preferably in Engineering or equivalent technical field.
6+ years of manufacturing/engineering experience
3+ years supervision preferred.
technical workforce preferred.
Knowledge of time keeping.
Experience working with International Standards Organization (ISO), Food and Drug Administration (FDA) and Good Manufacturing Practice (GMP) supervised environment.

Responsibilities

Lead production personnel to improve quality and output in a manufacturing operation.
Establishes personnel schedules and product lines based on business needs.
Supervises production operation and personnel to meet production goals.
Performs line Gemba walks.
Owns Platform audit and compliance readiness, including facilities work orders.
Ensure Compliance Wire curriculum is up to date/maintained by Platform needs.
Conducts performance reviews and provides feedback, including disciplinary actions as required.
Provides mentoring and supervision to technicians to safely operate, troubleshoot and maintain equipment.
Identifies, plans, implements, and facilitate improvements to the quality & efficiency of the manufacturing lines under moderate supervision.
Coordinating teams of technicians is vital for completion of projects.
Ensures adherence to safety, environmental, quality, and regulatory policies & procedures.
Identifies and revises safety, regulatory, equipment and process training documentation.
Develops and implements equipment and/or throughput improvements that will improve efficiency, product yield and safety.
Maintain flexibility to meet organizational needs.