Manufacturing Supervisor

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 https://www.jnj.com

Job Function:
Supply Chain Manufacturing

Job Sub Function:
Manufacturing Pharmaceutical Process Operations

Job Category:
People Leader

All Job Posting Locations:
Gurabo, Puerto Rico, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Manufacturing Supervisor to join our team in Gurabo, PR.

Summary:

The Manufacturing Supervisor is responsible for fulfilling the production/manufacturing schedule requirements in terms of quantity and due dates while maintaining the highest quality standards in compliance with company policies and procedures, and all applicable regulations.

They plan day-to-day manufacturing and/or packaging functional areas assigned and are accountable for the supervision, coaching, and development of assigned personnel.

The Supervisor uses their professional and technical expertise to resolve complex problems and will work with a variety of critical assignments, requiring analytical skills and critical thinking.

The Supervisor may serve as the area Sr.

Supervisor when required, and provide support during budget preparation, critical projects, and meetings.

Key Responsibilities:


* Ensure that department has adequate resources and capacity in personnel, equipment and materials to meet the planning demand.


* Monitor and control the process for its efficiency (yields, scrap, equipment downtime, personnel attendance, etc.).


* Fully responsible for developing and updating all areas SOP’s, JHA, Batch Records, forms and logbooks to reflect the manufacturing process and to be in full compliance with cGMP’s and EHS requirements and also perform systematic walkthroughs' audits of the operational floor.


* Responsible for on time and complete investigation of deviations on its area of control.


* Apply knowledge of the scientific principles involved in the Parenteral Manufacturing processes, including knowledge of raw materials, processes, quality control, costs, and other techniques for enhancing the effecti...