Quality Control (Lab Analyst) – Contract Employee

Business IntroductionWe 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; its 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 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ResponsibilitiesThis 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 YouWork 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 QualificationWe 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 QualificationIf 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 were 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 . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

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