Quality Operations Senior Specialist - 製薬会社

Location: Tokyo, Japan
Job Type: 正社員
Salary ¥6000000.00 - ¥12000000.00 per annum
Specialization: ライフサイエンス(医療機器・製薬・化学・ヘルスケア・農業・畜産)
職種 品質管理 / 品質保証
お問合せ Eureka Teramura
参照 JO-2002-436627
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※Applicants must have permission to work in Japan and required fluent ~ native level Japanese.

[Company Description]

  • 100ヶ国以上で事業を展開し、トップクラスの売上を誇る世界的企業


  • 開発費に投資は惜しまない
  • サイエンスを強く追求している会社・合理的
  • 「働き方改革」が流行するずっと前から仕事と生活が共に充実する職場を目指されてきた
  • 「ダイバーシティ経営企業100選」に選出されるなど高い評価
  • 離職率がとても低い、心地がいい
  • 安定、安心感が有難い。従業員は守られている・大切にされている
  • 新しい技術・今までやったことのないやり方をチャレンジしたいと思う人だとのびのび・楽しく仕事が出来る
  • 自身で考えて発信する方は歓迎される

■Position Overview - Basic Functions & Responsibility
Essential function(s) includes, but is not limited to:
This position is critical to ensure sustainable compliance of site products and processes, procedures and systems with our Manufacturing Division requirements and regulatory requirements and expectations.

Under his/her responsibilities fall the quality oversight for

  • Receipt, handling, storage, and disposition of bulk products, raw materials and components
  • Batch record review and Release related to components
  • Deviation investigations
  • Corrective and preventive actions (CAPA) investigation, management and approval
  • Audit Responses

The incumbent interfaces with all site functions and the global Quality organization (collaboratively with Quality Operations Manager) with regards to the above described activities. The incumbent should lead a team of 4 to 5 members whom responsible for above activities at our site.

■Primary Activities
Primary activities include, but are not limited to:

  • Establish adequate controls and procedures for the receipt, handling, storage, and disposition of components, containers and closures, in-process materials, packaging materials, labeling, drug substances incl. intermediates and drug products incl. intermediates.
  • Ensure that adequate processes and procedures are in place and followed for material release
  • Lead investigations related to the section with collaboration of other departments as needed. Also generate deviation reports, perform trend analysis of root causes on a periodic basis.
  • Manage corrective and preventive actions (CAPA) related to components, containers and closures, in-process materials, packaging materials, labeling, drug substances and drug products and associated facilities.
  • Perform Annual Product Reviews/Annual Product Quality Reviews of each product manufactured on site. Utilize annual data to identity system or process improvements and ensure their implementation, as appropriate.
  • Represent quality, provide quality oversight in complex projects or initiatives such as new product introduction.
  • Lead the team for continuous improvement initiatives and be act as a change agent to initiate such activities.
  • Manage Quality and supply KPIs related to the section in aligned with site Hoshin.
  • Establish skill development schemes for the team, be a part of talent development for the team.
  • Manage daily activities, issues through standard processes such as Tier.


  • Degree in Life Sciences, Engineering or related relevant discipline.
  • Minimum of 5 years' experience in the regulated pharmaceutical environment (pharma or medical device); preferably in a manufacturing site in quality (including QC) and/or manufacturing roles.
  • Leadership skills
  • Knowledgeable of Japanese and global authority quality and compliance requirements
  • Knowledgeable in Industry Best Practices for quality and compliance related topics.
  • Strong collaboration and cross-functional leadership skills to drive continuous improvement and promote knowledge sharing and implementation of best practices across the site and with other Quality functions on global and local level.
  • Team lead experience
  • Preferably have project management skills.
  • Be ready to act as change agent
  • Good Japanese and English communication skills (TOEIC 750 or more)

[Employment Type]
Full time

6M-12M yen
※Experiences and skills will be considered


Please click "apply" if you are interested in the job.
We will review your profile and contact you within five business days should we find that you satisfy the requirements of the hiring company.
Further details about the company and position will be notified at a later date.