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Quality Assurance Specialist - VIE Contract (W/M) APPLY FOR ROLE MY CANDIDATE ACCOUNT 気になる

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外資系製薬メーカー  統計解析プロジェクトリード

募集要項

業務内容

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

We are looking for: Quality Assurance Specialist - VIE Contract (W/M)
Target start date: 01/04/2023

Responsibilities:
・Initiated and executed an effective and efficient change control process in accordance to internal and external requirements
・Investigated and resolved NCRs -Non-Conformance Reports, Internal Audits, CAPAs - Corrective & Preventative Actions related to Documentation Services
・Assisted with reporting and analysis of Change Control metrics
・Knowledgeable about GQP- Good Quality Practice, and PMDA -Pharmaceuticals and Medical Devices Agency, FDA -Food and Drug Administration and ISO - International Organization for Standardization standards etc.
・Performed data review following staff performance of customer test requests in a timely and effective manner
・Confirmed that all customer requests for information pertaining to testing (or any other services) are met in a timely and effective manner
・Ensured that routine testing submitted by customers is completed within established parameters governing Company quality and regulatory compliance specifications
・Participated in the preparation and review process for appropriate department Standard Operational Procedures, worksheets and data forms
・Frequently communicated with other country’s operation manager to make sure/ keep quality the products
Administrative

語学力


ビジネスレベル

年収

500万~800万

給与

賞与 年3回
3月、6月、12月

雇用形態

正社員

勤務地

東京都

休日

年間休日122日
■完全週休2日制
休日:土日祝
■年末年始休暇 
(12/29-1/4)
■慶弔休暇 
■有給休暇 
(11日~20日)
■産前・産後休暇
(取得実績多数)
■育児休暇
(取得実績多数)
■母性保護休暇
■妊婦健診休暇
■5月1日
■フレキシブル休暇2日
■年次有給休暇(初年度11日/2年目以降付与日数増加、6年目以降毎年20日)
■ラ・メゾン休暇(「未使用で無効になってしまう有給休暇を活用する」ための制度)など

福利厚生

各種保険完備

健康診断、予防接種、健康増進活動
ラ・メゾンルーム
社内マッサージサービス
結婚、出産祝金、弔慰金、妊娠時検査補助金、入院見舞金、災害見舞金等の支給
社宅制度、住宅手当、確定拠出年金、確定給付年金、DCマッチング拠出(企業型)
財形貯蓄、持ち株制度、福利厚生倶楽部

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事業内容

医薬品等の製造販売・輸入、研究開発

業種分類

メディカル/医薬品メーカー

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