Johnson & Johnson

Makes prescription drugs and medical devices

Operations Staff

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours

Full-timeSunto District, Shizuoka, JapanNo salary listed

About the Job

Requirements

High school graduation or an equivalent qualification is required.
Fluency in Japanese at JLPT N1 level is required.
The candidate must be comfortable using translation tools to understand English emails.

Responsibilities

Lead inspection, manufacturing, and storage operations according to the correct procedures and schedule to consistently produce products of the correct quality.
Become fully proficient in operations within the assigned area of responsibility.
Be responsible for safety and quality during inspection, packaging, and storage work.
Manage manufacturing schedules across pharmaceutical inspection, packaging, and operations lines within a shift system.
As a team member, actively pursue continuous improvement and operational efficiency in work efficiency, safety, and quality management.
Actively lead the development of a continuous-improvement culture at the factory.
Complete all required training by the deadlines to comply with Good Manufacturing Practices.
Coordinate team discussions from initiation through closure of quality investigations when work deviations or quality issues arise, determine responses, and prevent recurrence.
Prioritize compliance with quality, safety, and regulations.
Comply with applicable laws, Good Manufacturing Practices, company rules, site policies, and procedures.
For existing-product assignments, be willing to work day and night shifts; the listed night shift is 18:45–03:45 with a one-hour break.
For new-product assignments, after product launch and depending on production conditions, be able to work occasional weekly shift blocks starting between 11:00 and 13:00 and ending between 20:00 and 22:00, approximately once or twice per month.

Desired Qualifications

A university degree or higher in pharmaceutical or biological sciences.
Knowledge of and practical experience with Good Manufacturing Practices or Current Good Tissue Practice.
Knowledge of or experience with Lean or Six Sigma.
At least two years within the last ten years of laboratory experimentation, research, or employment at a university or company, regardless of whether the work was academic or professional.
Willingness to improve English skills in the future.

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:

Professional

All Job Posting Locations:

Sunto, Shizuoka, Japan

Job Description:

■職務概要

・正しい手順で時間通りに検査、製造、保存する作業のオペレーション業務をリードし、正しい品質の製品を継続的に製造する。

■主な職務及び主な責任

候補者の経験値及び適性に応じて、既存製品の製造オペレーション、もしくは、新製品のオペレーションをご担当いただきます。

・正しい手順で時間通りに検査、製造の作業のオペレーション業務をリードし、正しい品質の製品を継続的に製造する。

・責任分野におけるオペレーションに100%精通する。

・検査・包装・保存作業において、作業の安全性、品質に関して責任を持つ。

・シフト体制の中で、医薬品の検査・包装・オペレーション作業の各ラインでの製造スケジュール管理を行う。

・オペレーションにおける作業効率、安全面、品質管理において、継続的な改善や業務効率をあげる努力をチームの一員として積極的に行う。

・工場内の改善カルチャー醸成を積極的に導く。

・GMP遵守のため、各種決められたトレーニングを期日までに完了する。

・作業逸脱、品質問題が起こった場合にはQIの起票からクローズまでのチーム内での協議を取りまとめ、対応の決定及び再発防止に努める。

■法規制の順守に関する責任

・品質、安全、コンプライアンスの順守を最優先とする。

・法規、GMP及びすべての社則・サイトポリシー・手順を遵守する。

応募資格：

【必須（MUST）】

・高等学校卒業、もしくは同等の資格を有すること

・薬事、生物学系の大卒業以上の資格があるとなおよい

・日本語流暢（JLTP1レベル）、英語のメールは翻訳機などを使用して理解することに抵抗がないこと

【歓迎（WANT）】

・GMP/CGTP知識と現場経験　

・リーン、シックスシグマ知識・経験

・仕事研究問わず、直近１０年で２年以上の大学内もしくは企業内でのラボでの実験・研究・就業の経験

・英語を将来的に向上させる意欲

【行動特性】

・コラボレーションとチームワーク　

・誠実なクレドバリュー

・顧客重視

・EHSルール及び手順の遵守

・インシデント、ニアミス等の報告

【勤務形態について】

既存製品担当：日勤及び夜勤（18:45-03:45　休憩１時間）がシフト体制で入れることが望ましい。

新製品担当：製品上市後、生産状況によっては、11:00-13:00の間での勤務開始～20:00-22:00の間での勤務終了（休憩１時間）のシフトが月1-2回、１週間単位で発生する可能性があります。

Required Skills:

Preferred Skills:

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size: 10,001+
Company stage: IPO
Headquarters: New Brunswick, NJ
Founded: 1886

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