[Innovative Medicine] Staff, Quality Control Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant)

Japan·Shizuokalead

OtherQuality Control

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Quick Summary

Requirements Summary

科学、化学、生物学、バイオテクノロジー、微生物学、関連分野の学士号もしくは同等の教育医薬品業界における 3 年以上の業務経験 GMP準拠環境下における分析業務またはラボシステム関連業務の経験 Bachelor's degree or equivalent education in science, chemistry, biology, biotechnology, microbiology,

Technical Tools

OtherQuality Control

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.

Quality

Supplier Quality

Professional

Shizuoka, Japan

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

Responsibilities

~1 min read

教育/経験Education and Experiences:

→科学、化学、生物学、バイオテクノロジー、微生物学、関連分野の学士号もしくは同等の教育

→医薬品業界における 3 年以上の業務経験
→GMP準拠環境下における分析業務またはラボシステム関連業務の経験

→Bachelor's degree or equivalent education in science, chemistry, biology, biotechnology, microbiology, or related fields.

→Over 3 years of work experience in the pharmaceutical industry
→Experience in laboratory or laboratory systems-related activities under GMP-compliant conditions

知識、資格、及び技能 Knowledge, Qualification and Skills:

→GMP/GCTPとデータインテグリティ

→医薬品の規制、基準、およびガイドライン

→分析試験/ 機器分析/ 機器管理文書化 (SOP、WI、ラボワークシート、および評価)

→Microsoft Officeなどの基本的な PCソフトウェアプログラムおよびEmpowerなどの分析ソフトウェアプログラム (データ入力、データ分析、ワードプロセッシング、プレゼンテーション、および計算のためのソフトウェアアプリケーションの使用)

→英語でのコミュニケーション（メール/会議）

→GMP/GCTP and Data integrity

→Pharmaceutical regulations, standards, and guidelines

→Experience in analytical testing, instrument analysis, and equipment management

→Proficiency in documentation (e.g. SOP, WI, lab worksheet, and assessment)

→Ability to use basic PC software, including Microsoft Office and analytical software such as Empower (usage of software applications for data entry, data analysis, word processing, presentations, and calculations)

→Good communication skills in English (both written and verbal)

行動特性Core Competencies:

→確固たるクレド―バリュー

→EHS 規則と手順の遵守

→すべてのインシデント、事故、およびニアミスイベントの報告

→コラボレーションとチームワーク

→Credo value of integrity

→Compliance with EHS rules and procedures

→Report all incidents, accidents, and near missed events.

→Collaboration and teamwork

#LI-Onsite

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社内公募ガイドライン

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在籍期間に関わらず、書類選考を通して１次面接に進んだ場合は、社内公募に応募し選考に進むことを上司に報告してください。
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Nice to Have

~1 min read

Analytical Reasoning, Business Behavior, Compliance Management, Controls Compliance, Cross-Functional Collaboration, Execution Focus, ISO 9001, Issue Escalation, Performance Monitoring, Persistence and Tenacity, Quality Auditing, Quality Control (QC), Quality Standards, Quality Systems Documentation, Report Writing, Technologically Savvy, Vendor Selection