Live opening · Posted 6 hours ago

Process Coordinator

Janssen-Cilag Limited · Kiryat-Ono, Tel Aviv District, Israel
Workday
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At a glance

The key details from the original listing.

Posted 6 hours ago
CompanyJanssen-Cilag Limited
LocationKiryat-Ono, Tel Aviv District, Israel
SourceWorkday
ListedPosted 6 hours ago

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About the role

Description supplied by the original job listing.

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.
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Pharmaceutical Process Operations
Job Category:
Business Enablement/Support
All Job Posting Locations:
Kiryat-Ono, Tel Aviv District, Israel
Job Description:
Responsible for performing a variety of tasks related to the processing of ingredients and/or pharmaceutical products. Operates general manufacturing equipment, such as autoclaves, ovens, stills and filtration apparatus. Handles raw materials and intermediate or finished products. Mixes compound ingredients for liquid products, suspensions, ointments, mixes or blends for tablet granulations and capsule powders. Performs general maintenance as required on pumps, homogenizers, filter presses, tablet compression machines, etc. Performs standard operating procedures to meet current Good Manufacturing Practices (GMP) and maintaining records as required. Completes tasks in compliance with all regulatory requirements. Participates in program or functional team projects developing process improvement methods, solutions and procedures to enhance program quality, cost and scheduling.
Required Skills:
Preferred Skills:
Agile Manufacturing, Analytics Dashboards, Chemistry, Manufacturing, and Control (CMC), Communication, Data Compilation, Data Savvy, Execution Focus, Gap Analysis, Good Manufacturing Practices (GMP), Issue Escalation, Operational Excellence, Pharmaceutical Industry, Plant Operations, Proactive Behavior, Problem Solving, Process Optimization, Project Administration, Quality Auditing

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