Operations Manager, Process & Procedures

Are you passionate about streamlining processes and creating impactful procedural documents? Join our Global Development team as an Operations Manager, Process & Procedures, where you’ll drive the development and management of our controlled procedural document portfolio. This role offers the opportunity to contribute to process innovation and collaborate with cross-functional teams in a dynamic, regulated environment. Based in Tokyo, this position is your chance to make a meaningful impact while advancing your career.

A Typical Day:

• Lead the revision and creation of procedural documents through their lifecycle, including updates for process improvements and administrative changes.
• Facilitate process mapping and content updates in collaboration with authors and subject matter experts (SMEs).
• Support procedural document projects by partnering with functional owners and cross-functional SMEs to improve existing processes.
• Coordinate review cycles and approval workflows for assigned procedural documents.

This Role May Be For You If:

• You thrive in a collaborative environment and enjoy working with cross-functional teams to achieve shared goals.
• You are detail-oriented and excel at identifying gaps in processes and proposing innovative solutions.
• You have strong organizational and project management skills, balancing multiple priorities with ease.
• You possess expertise in controlled procedural document principles and process design.
• You are proficient in tools like Microsoft Visio for process mapping and have experience with electronic document management systems.
• You value integrity and trust, and you’re skilled at negotiating and influencing at all organizational levels.
• You enjoy strategic thinking and problem-solving in a regulated environment.

To Be Considered:
Candidates must have a Bachelor’s degree and at least 5 years of experience in a global regulated organization, with 3 years in a quality role focusing on procedural documents. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements, as well as experience in controlled document principles, is essential. Preferred qualifications include expertise in Microsoft Visio or similar tools and familiarity with electronic document management systems.

本ポジションにご興味をお持ちいただけましたでしょうか。みなさまのご応募を心よりお待ち申し上げております。我々の企業理念であるRegeneron Wayを共に歩む、その第一歩を踏み出しましょう。当社では、多様性を大切にする企業文化に基づき、幅広い内容の福利厚生をご用意しております（内容は地域によって異なります）。米国の場合、ヘルス＆ウェルネスプログラム（医療保険、歯科治療や眼科治療に関する保険、生命保険および身体障がいに関する保険など）、フィットネスセンター、確定拠出年金（401k）、家族支援制度、株式報酬、年次ボーナス、有給休暇、および特別有給休暇制度（例：育児休暇、軍務休職）などがあり、対象となる社員の方であれば、すべての職位においてご利用いただけます。当社の、米国における福利厚生の詳細に関しましては、https://careers.regeneron.com/en/working-at-regeneron/total-rewards/をご参照ください。その他の国における福利厚生に関しましては、採用担当者までお問い合わせください。
最高の仕事を通じて最もすばらしい成功を手にするためには、社員が一丸となって働くことこそ重要である、という信念に則り、当社では多くの職種において、オフィス勤務を必須とさせていただいております。オフィス勤務に関する当社のポリシー、および勤務内容や勤務地に関するみなさまお一人おひとりの個別の条件につきましては、採用担当者にお問い合わせください。