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QC Analyst(名古屋)

Date: Jan 11, 2019

Location: Nagoya, JP, 453-0801

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Job Description

原薬・添加剤の分析法バリデーション試験 試験責任者

新規原薬・添加剤の品質評価 試験責任者
原薬・添加剤の分析法バリデーション試験 試験責任者

Qualifications

【必須(MUST)】

【必須経験】
・医薬品のCMC分析試験 試験責任者以上の役職経験
・分析法バリデーション,ベリフィケーション
・試験操作手順書,標準操作手順書の作成

【必須知識】
・日本薬局方全般
・CMC分析技術
・GMP
 

【歓迎(WANT)】

・変更管理業務

・英語(初級~中級レベル)
・分析法バリデーション
・薬剤師資格

協調性のある方
変化を楽しめる方

【歓迎要件】
転職活動が初めての方

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

In process of validation

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.