Production Planning & Scheduling Specialist

Johnson & Johnson Innovative Medicine•San Lorenzo, PR

About The Position

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Requirements

Bachelor’s Degree in business, engineering or operations is required.
A minimum of one year of related work experience is required.
Manufacturing Supervisor experience, Supply Chain Management experience, FG planning or Capacity Planner preferred.
Experience in using ERP system, JDE preferred.
Experience in Advance Planning System preferred.
Demonstrate leadership ability, self-starter, decisive, self –motivated, and desire to work in a team environment.
Strong analytical and problem-solving skills.
Bilingual (Spanish & English).
Availability to work various schedules, which may include 1st, 2nd, 3rd shifts and/or 12-hour daily shifts, including weekends and holidays.
Advance computer skills and use of software application(s). (Microsoft Office)
Excellent verbal and written communication skills required inter-facing with all levels of associates throughout the company.
Experience in using ERP system, JDE preferred.
Experience in Advance Planning System preferred.
Ability to manage multiple projects in a changing environment while still meeting deadlines.
Demonstrate leadership ability, self-starter, decisive, self –motivated, and desire to work in a team environment.
Strong analytical and problem-solving skills.
Ability to anticipate and communicate impact of changes.

Nice To Haves

Manufacturing Supervisor experience
Supply Chain Management experience
FG planning or Capacity Planner preferred.
Experience in using ERP system, JDE preferred.
Experience in Advance Planning System preferred.

Responsibilities

Responsible for Finish Goods and Sub Assembly weekly plan for the responsible areas.
Monitor Raw Material availability, constraint and align capacity usage and ramp up as needed.
Work with PPL Leader to align monthly volume commitments to set up System Capacity.
Monitor planned vs. actual outputs, set-up temporary design changes, ensure production is not schedule over major preventive maintenance. In addition, provides guidance for optimal Preventive Maintenance timing.
Proactively monitor and address production disruptions that may impact Customer Service.
Responsible to analyze and resolve with Business Unit Manager any short-term capacity planning.
Accountable for explaining and monitoring execution versus Weekly Plan and Monthly PSR.
Participated and support Integrated Production Teams (IPT) for manufacturing line (s).
Recommends if additional capacity is needed and align with Business Unit Managers.
Responsible for managing re-introduction of material on-hold and salvage.
Responsible for communicating Available to Promise to Affiliate and Domestic locations for product.
Trend analysis for future demand in areas of starts/transfers.
Work with project team and event planner when product conversions and transfers.
Responsible for ensuring Inventory Targets are met.
Provide information for scorecard reports.
Dosimetry Audit and Bioburden Audit sampling program coordinator.
Key contact with supply planning to manage events and receive CTR factor information if necessary.
Comply with all environmental, safety and occupational health policies (i.e., ISO14001 & OSHAS 18001).
Responsible for communicating business related issues or opportunities to next management level.