【大手外資製薬企業】Process Improvement Lead

製造現場で発生する逸脱やその他全ての品質インシデントを処理し、製造部門と品質保証の架け橋となる

仕事内容

As a Process Improvement Lead you are expected to handle deviations and all the other quality incidents that happen on the shop floor and act as a solid bridge between Production and QA. You will also drive the optimization journey in shop floor together with production management and other key functions within while closely collaborating with other parts of global Product Supply for process standardization representing .

Your goal will be to implement and anchor robust production systems and processes in shop floor to eliminate potential/actual root causes of errors with higher hierarchy of control (HoC) in place and ultimately to reduce the number of deviations. At the same time, it is required to keep the site aligned with peers in the rest of Product Supply by proactively introducing globally standardized process.
Other tasks include, but are not limited to:

Tackle quality deviations that happen on the shop floor and interact mainly with QA (sometimes with QAs from global organizations), and propose and implement higher HoC with Line managers, process supporters and/or LEAN Professional if necessary
Continuously optimize and standardize shop floor processes by utilising LEAN tools and by introducing global or industry standard
Well understand and identify business needs and translate them into viable and sustainable solutions and keep the Production leadership team updated on potential opportunities for process improvements.
Participate in relevant Process Group (PG) and/or global projects as representative to , share what is discussed therein with leadership team and lead the implementation, change management. Drive the LEAN related agenda in Production area with relevant stakeholders.
Support Operation Responsible (OR) with validation activities that include but not limited to validation planning, risk assessment, documentation, change control including (Organizational Change Management) OCM, and work closely align with Training Partner to implement more robust, more agile and simpler training system especially for shop floor operators.

応募条件

【必須事項】

・Minimum bachelor’s degree in Engineering, Manufacturing, Mathematics, ・Statistics, Pharmaceuticals, Technology, Project Management, or any other relevant fields.
・Minimum of 5 years of hands-on experience working in in Production, Manufacturing, or Operations environment (pharma companies preferred), delivering process improvements or change management.
・Be a strong logical thinker with both right quality mindset and basic statistic competency.
・Business-level in English and Japanese (writing and speaking) are required.

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

学歴

大学卒以上

雇用形態

正社員

試用期間

6ヶ月

勤務地

福島

転勤の有無

転勤なし

受動喫煙防止措置

屋内禁煙

勤務時間

フレックスタイム制
フルフレックス（コアタイムなし）

勤務開始日

応相談

休日休暇

年間休日数：129
土日祝
年間有給休暇：入社半年経過時点10日　10日 ～ 20日
法定休暇：年次有給休暇、産前産後休暇、介護休暇
その他休暇：ボランティア休暇、リフレッシュ休暇など

年収・給与

年収　　700万円～　経験により応相談

諸手当

通勤手当（全額支給）、時間外手当、住宅手当、その他各種手当有
MRの場合上記に加え、営業手当、外勤日当を支給

昇給

年1回

賞与

年2回

採用人数

若干名

待遇・福利厚生

通勤手当：有
確定拠出年金制度

各種制度

健康保険：有
雇用保険：有
労災保険：有
厚生年金：有

選考プロセス

１）書類選考
２）一次面接
３）最終面接