【今市】Quality Control (Lab Analyst) – Contract Employee

Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Position Summary あなたは今市の品質管理ラボチームの一員として、試料の受入れ・検査・記録を担当します。現場のチーム、製造、品質システムと協力して、試験が社内基準や法規制に適合するようにします。私たちは誠実さ、注意深さ、学ぶ意欲を重視します。この役割は技術力を伸ばし、責任範囲を広げる機会を提供します。あなたの仕事は、科学・技術・人材を結集し、共に病に先んじるというGSKの使命に直接つながります。 Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - 受入試料、原材料、中間体、製品の定期的な分析試験を承認済み方法で実施する。 - 試料の受領・登録・前処理・保管を規程に従って行い、試験結果を正確に記録する。 - 試薬・標準品や装置の簡単な準備・点検・清掃を行い、日常の機器管理を支援する。 - 結果を仕様と照合し、逸脱や異常傾向を速やかに報告・記録する。 - 調査や非適合対応のサポート、改善活動やプロジェクトへの参加を行う。 - 安全、衛生、データ完全性に関する現場ルールと手順を順守する。 Why You? Work arrangement 本ポジションはオンサイト（出社）での勤務となります。シフトや勤務時間は施設の運用に合わせて決まります。現地で協働できる方を求めます。 Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - 高等学校卒業以上。理系（化学、生物、バイオ、臨床検査等）を専攻していると望ましい。 - ラボでの実務経験または実習・インターン経験があること（品質管理、試験業務を含む）。 - 基本的な分析手技や試料取扱いの知識と安全対策の理解。 - 文書化や記録管理を正確に行う注意力。 - 書面・口頭でのコミュニケーション能力とチームで協力する姿勢。 - オンサイトでの勤務が可能で、職場の安全規則に従えること。 Preferred Qualification If you have the following characteristics, it would be a plus - 大学、短大、専門学校で化学・生物・バイオ関連の学位または専攻を修了している。 - 規制環境（医薬品、バイオ等）でのQCやラボ業務経験。 - 基本的な分析機器（分光光度計、クロマトグラフィー等）や微生物学的手法の知見。 - LIMS（ラボ情報管理システム）や電子データ記録の使用経験。 - 問題解決や原因分析に参加した経験、継続的改善活動への貢献経験。 - 英語の読み書きに抵抗がなく、技術文書を参照できること。 What we value 私たちは誠実さと透明性を大切にします。互いに敬意を持ち、学び合う文化を育てています。違う視点や背景を歓迎し、誰もが安心して貢献できる職場を目指します。あなたが持つ丁寧さや学ぶ意欲は、チームの成長と患者への貢献につながります。 Ready to apply? この役割に興味がある方は、履歴書と短い自己紹介（なぜ応募するか、どんな貢献ができるか）をお送りください。あなたと一緒に働けることを楽しみにしています。

Skills

Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact [email protected]. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

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