Manufacturing Process Specialist (Batch Record)

Johnson & Johnson•Gurabo, PR

22h•Onsite

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. About Innovative Medicine Our expertise in Innovative Medicine is recognized 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 Process Specialist (Batch Record) to be in Gurabo, PR! You will be responsible for implementing significant improvements in the Operations areas using best practices, methodologies, Process Excellence tools, and Key Performance Indicators. This includes leading, planning, and completing projects, coaching project teams, and fostering a continuous improvement and lean culture. Collaborate with support groups and transactional areas to reduce costs, minimize inventory, and create a smooth workflow aligned with customer demand. Also works with Business Excellence to develop and maintain current and future state Value Stream Maps (VSM) to identify areas for improvement. Duties include prioritizing and tracking the progress of projects and initiatives, providing training on Process Excellence methodologies, supporting Process Excellence certification efforts, conducting statistical analysis, and contributing to employee engagement. Serve as a change management agent for new initiatives, using tools such as dashboards, scorecards, and visual factory techniques.

Requirements

Bachelor’s or higher degree is required; focus in Science, Pharmacy, Engineering, or a related field is preferred
Experience in the pharmaceutical or related industry, performing scientific, manufacturing activities, and/or project management.
Fluent in English and Spanish both spoken and written
Excellent communication skills and strong technical writing abilities
Proficient in the use of Microsoft Office, including Word, Power Point, Excel, and Outlook

Nice To Haves

Project Management, Statistical Analysis, and/or Process Excellence certification is a plus
Knowledge of Current Good manufacturing Practices, Regulatory Compliance, and Aseptic Techniques
Proficient in MS Project, ePES systems, and Checklyst Management Program
Knowledge of Lean Methodology and other Process Excellence tools
Good knowledge of Safety and Environmental requirements.

Responsibilities

Provides technical support in planning, developing, and implementing continuous improvement and transformational projects using standards, and Process Excellence tools.
Defines strategies to optimize product costs, including reducing waste, minimizing changeover time, streamlining product flow, and other relevant areas.
Conducts basic research on new technologies for potential application.
Meets with stakeholders to facilitate the conversion of business needs into actionable project cases aligned with strategic goals.
Supports the preparation of technical documentation, such as strategic plans, protocols, and reports, related to projects.
Engages employees in a continuous improvement environment through activities such as Kaizen teams, generating improvement ideas, supporting Process Excellence certifications, and other initiatives.
Coordinates Gemba walks, tracks identified actions, and monitors participation and progress.
Provides support to Managers and Supervisors in day-to-day process activities.
Documents all work-related activities clearly and accurately, adhering to established company and regulatory compliance requirements.
Adheres to all company policies, procedures, programs, systems, rules, and regulations related to safety, environmental practices, quality, record management, human resources, security, and other compliance areas, and encourages co-workers to do the same.
Reports any violations or deviations to immediate supervisors or compliance area officers.