品質保証 - 製薬会社

Location: Fukushima, Japan
Job Type: Permanent
Salary: ¥7000000.00 - ¥12000000.00 per annum
Specialization: Life Science (Medical Devices / Pharmaceutical / Chemical / Healthcare / Agriculture / Livestock),
Sub Specialization: QC / QA,
Contact: Eureka Teramura
Reference: JO-2011-450760
about Eureka Teramura

※Applicants must have permission to work in Japan and required fluent ~ native level Japanese.

[Company Description]
外資系製薬会社

  • 「働きがいのある会社」にもランクインされる、糖尿病などの製品を手掛ける会社です
  • 社内公募制度が充実しており、ジョブローテーションもあり、キャリアパスを自分で作りたい人にはぴったり

[Responsibilities]
Key Responsibilities

  • Regulatory responsibility
  • Project member
  • QA oversight

Main Job Tasks
■Regulatory responsibility (30%)

  • Maintain business licence, responsible for GMP inspection
  • Review the application sheet for new product launch
  • Lead the internal audit
  • Trainer of GMP and quality mindset

■Project member (30%)

  • Member of the KFA local project in terms of quality

■QA oversight (30%)

  • Take initiative to implement and manage the process

[Requirements]
■Education

  • University graduates, preferable to have pharmacist license

■Experience

  • At least three years working at QA area

■Personal Skills

  • Communication, Negotiation, Presentation, fair decision, business ethics compliance, advanced English communication

■English/Japanese

  • TOEIC 800 or above
  • Capable to negotiate, propose, and give presentation in English
  • Capable to participate in Telephone/Video Conference

[Employment Type]
Full time

[Salary]
7.2M-11.6M yen
※Experiences and skills will be considered

[Location]
Fukushima


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