QC Chemist, Koriyama Factory
この求人にエントリーする
求人No. 161758
募集要項
業務内容 |
■About the department For 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Novo Nordisk's new drug development portfolio is rich, and we expect to launch many more formulations in the future. The Quality Control Department is also constantly working on new tasks for new developments as well as routine tasks. Therefore, this is a very rewarding job with many opportunities to be exposed to cutting-edge formulations and logical technologies. As a QC chemist, you will have the opportunities to go on business trips to receive the technology transfer in regards to the new products at the headquarters in Denmark, and also many other opportunities to collaborate with the global quality team on a daily basis. You will be able to experience the technology of the world's leading company in diabetes treatment on a global level. ■The position As a QC Chemist, you are to manage the QC projects/activities methodically and properly according to the product specifications and Quality Control Standard Code. You are also expected to enhance the relationship between the QC relevant stakeholders in order to assure the internal compliance with the support of QC Team Leader/specialist when needed. The key responsibilities include (but are not limited to): ・Lead QC technician/s to perform the requested examination and accordingly contribute to the stable supply of high-quality products and accelerating the continuous improvement of the annual routine tasks to seek for higher efficiency, ensuring the compliance of requirements by gathering and grasp of the latest Japanese regulations to create or update the relevant contents. ・Properly manage QC tasks, including reception control evaluation, release evaluation, PPM (Printed Packaging Material) evaluation, etc. Improve processes/procedures by implementing MRA (Mutual Recognition Agreement), considering QC test outsourcing, and introducing TGS (Tail Gate Sample)/certified suppliers for higher efficiency. ・Contribute to stable supply of high-quality products through QC equipment/machine/system management plan. Ensure compliance of QC process and operations with SOPs (Standard Operating Procedures) and other requirements. ・Implement Global IT compliance improvements (Global LIMS, Global Empower3, Planner) as new global systems for all processes according to QC plan. ・Have knowledge of the latest global SOP and Japanese regulations to ensure regulatory compliance and enhance team members' collaborative awareness to ensure the timely launch of new products. Support technicians in performing requested examination for new product launch or handling customer complaints. |
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語学力 |
要 ・FJapanese and English communication skills (email, Teams/Face-to-Face meeting etc.) are essential. |
給与 |
年俸制 賞与 年2回 ※前職を考慮して決定 |
雇用形態 |
契約社員 |
勤務地 |
福島県 |
通勤交通費 |
全額支給 |
休日 |
年間休日122日 【休日】 土 日 祝日 【休暇】 年末年始休暇 【休暇メモ】 ■慶弔休暇、育児休業、介護休業 ■積立休暇制度 ■年次有給休暇(初年度12日 最高20日) |
福利厚生 |
各種社会保険完備 営業手当 日当手当(営業外勤日3000円~/日)■昇給年1回(4月) ■財形貯蓄 ■企業年金 ■退職金 ■慶弔見舞金制度 ■研修制度 ■借上社宅制度 ■クラブ活動、保養所 ほか ※借り上げ社宅制度:補助(6.5万円~11万円)エリアと世帯数によって金額が異なります。 |
企業情報
事業内容 |
医療用医薬品、医療機器の開発、輸入・製造、販売 |
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業種分類 |
メディカル/医薬品メーカー |
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