Japon

QA Manager/ Life Sciences [Professional haken]

Emploi Japon

Titre du poste : QA Manager/ Life Sciences [Professional haken]

Entreprise :

Description du poste : 求人の要約 給与 年収 600 〜 800万円 職種 品質マネージャー, ディレクター, ヘッド 勤務地 東京23区求人詳細■Work conditions
・Temp-to-Perm
・Telework possible
・Location: Tokyo
・Hourly wage: Up to ¥3,000 – 5000 (Annual salary: Up to ¥8 million)Lead a dynamic team, ensuring top-tier quality in a cutting-edge life sciences environment.■About the company
Our client is a pioneering life sciences company committed to delivering innovative pharmaceutical solutions. They foster a collaborative and supportive work environment where continuous learning and professional growth are highly valued. They are seeking a highly skilled and experienced QA Manager to join their team.■Role & Responsibilities
You will oversee all aspects of quality assurance, ensuring compliance with Japanese regulatory requirements. You will lead a team, mentor junior staff, and collaborate with cross-functional teams to guarantee the highest quality standards in all processes, from research and development to commercialization. You will play a pivotal role in the company’s success.■Main tasks include
・Lead preparation of pharmaceutical documents for submission to Japanese regulatory authorities.
・Ensure compliance with regulations related to ethical pharmaceuticals, OTC, and regenerative medical products.
・Conduct GMP audits of manufacturing sites.
・Review QA submission documents, assess change controls, and manage batch release of commercial products.
・Oversee QMS, SOPs, vendor audits, and market complaint handling.
・Support GMP inspections by PMDA and other relevant authorities.
・Manage departmental goals, budgets, and training of subordinates.If you are interested in this exciting opportunity, apply now.
We look forward to hearing from you.
#LI-Hybrid こんな方を求めています経験・スキル ■Requirements
・Minimum 10 years of experience in a QA role within the pharmaceutical industry.
・Minimum 3 years of experience as a QA Manager or QC Manager for Type I, Type II, or regenerative medical products.
・University degree or higher in a biological science (medicine, pharmacy, science, agriculture, etc.); doctoral degree preferred.
・Expert knowledge of Japanese pharmaceutical regulations (PMDA and MHLW).
・Proven experience conducting GMP audits and supporting regulatory inspections.
・Experience reviewing manufacturing documents, deviations, change controls, and CAPAs.
・Excellent written and verbal communication skills in English and Japanese.
・Proven ability to lead and manage a team.
・Experience preparing presentations and communicating complex information clearly.
・Strong understanding of QMS, SOP development, and vendor management. 学歴 大学卒業以上 募集要項職種 品質マネージャー, ディレクター, ヘッド 給与 年収 600 〜 800万円 賞与 – 雇用形態 契約社員 雇用期間 期間の定めなし 就業時間 09:00~18:00 休日休暇 土曜日 日曜日 祝日 保険 健康保険 厚生年金保険 雇用保険 受動喫煙防止措置 敷地内禁煙 業種 医療機器・医療品関連※詳細はお仕事のご紹介時にお伝えしますランスタッドは、すべての⼈に平等に機会が与えられ、その可能性を引き出し、多様な経験と個性を社会の発展につなげていけるようサポートしていきます。

Salaire attendu : 6000000 – 8000000 per year

Localisation : 東京23区内

Date du poste : Tue, 20 May 2025 22:29:31 GMT

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Artia13

Depuis 1998, je poursuis une introspection constante qui m’a conduit à analyser les mécanismes de l’information, de la manipulation et du pouvoir symbolique. Mon engagement est clair : défendre la vérité, outiller les citoyens, et sécuriser les espaces numériques. Spécialiste en analyse des médias, en enquêtes sensibles et en cybersécurité, je mets mes compétences au service de projets éducatifs et sociaux, via l’association Artia13. On me décrit comme quelqu’un de méthodique, engagé, intuitif et lucide. Je crois profondément qu’une société informée est une société plus libre.

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