CMC薬事シニアマネージャー~定年65歳の優良企業!~

Job Details

<求人タイトル>

17640 CMC薬事シニアマネージャー~定年65歳の優良企業!~

<職務内容>

・Providing Japanese strategic and operational regulatory CMC expertise and support in cross-functional teams, as required, and working flexibly within and across regions to provide broad operational support to ensure the delivery of project/products and business objectives.
・Preparation and delivery of CMC regulatory operational plans for products in Japan and supporting the preparation and delivery of regulatory submissions.
・Responsible for submission from defining and agreeing content with CMC global team to executing reviews as required to ensure complete, concise and accurate submissions to PMDA in Japan with CMC Regional Regulatory Lead.
・Writing and / or Review of Japanese CMC submission documents and responses to PMDA questions
・Managing CMC aspects of routine and non-routine regional Health Authority interactions including issue resolution and negotiation of approvals, as delegated.
・Monitoring changes in the regulatory CMC environment in Japan to support and advise CMC global lead and teams with Regional Regulatory Lead.
・Providing input into regulatory CMC risks assessment and mitigation plans from a regional
perspective for Japan and ensuring that it remains in line with the overall global regulatory CMC strategy
・Coordinating and completing regulatory assessments of CMC changes in the designated systems
・Responsible for supporting Regional Regulatory Lead and maintaining open lines of communication with them on assigned projects/products to ensure awareness on status and issues relating to submissions in Japan.
・Responsible for leading or assisting in delivery of project assignments supporting business
needs e.g. representation of RegCMC on cross functional work streams
・Responsible for leading or assisting in delivery of RegCMC initiatives and the development of RegCMC standards and SOPs in Japan, as assigned.
・Ensure that appropriate records are maintained in the designated system for submission in
Japan

<応募要件>

・BS University degree in Life Sciences, Engineering, Biotechnology, or relevant Pharmaceutical Science
・Fluent English:spoken and written
・At least 5~7 years relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity, with at least 5 years of experience in Regulatory CMC and preferably 2 years professional experience in pharmaceutical manufacturing, analytical development, and quality assurance/control or related technical field.
・For at least two late phase development products or commercial product, interact with Global RegCMC team and relevant Biogen Japan departments with strong leadership as Japan CMC lead
・Successful authoring and contribution to delivering CMC submission documents of development and marketed products (biological, oligonucleotide, chemical entities and/or gene therapy products)
・Broad background of registration experience gained from working in the pharmaceutical
industry or a regulatory authority in one of the ICH regions on development and postapproval products
・Experience of direct communication and negotiation with regulatory agencies on CMC matters
・Knowledge of GMP requirements and standard systems (e.g. change management systems)
・Demonstrated competence in leading cross-functional teams and operating within a matrix
organizational structure
・Ability to work, with responsibility, both independently and within project teams or committees to attain group goals and key project milestones.
・Ability to solve problems in complex environments.
・Ability to project and timeline management.
・Ability to budget planning/management.
・Demonstrated inclusive leadership and emotional intelligence, along with verbal and written
remote working communication abilities.
・Demonstrated strategic thinking, change champion leadership, and risk assessment, including ability to integrate overall business objectives into the goals/vision/values of department and to communicate these effectively.
・Demonstrated competency in operations, planning, project management and tracking projects of high complexity and risk with clearly defined critical paths.
・Proven ability to manage projects across global locations/time zones. Proven ability to create strong, productive working relationships in a global setting with many different cultures.
・Enthusiastic orientation to teamwork. Works inclusively and collaboratively, effectively and
efficiently with others internally and externally. Strong conflict resolution skills: proven abilities to effectively and expeditiously reach satisfactory resolution among all involved parties.
Preferred requirements:
・Knowledge for Japanese regulation of regenerative drug product’s category
・Experiences for gene therapy product’s development
・Graduate degree preferred

<会社概要>

革新的医薬品の開発に取り組むグローバルバイオファーマです。現在新薬発売に合わせ、日本法人の組織体制も充実させるとともに、社員の働きがいを後押しする人事制度の拡充も図っています。

就業時間: 9:00-17:30(フレックスタイム制適用あり)

<注目ポイント>

同社の重点領域であり豊富なパイプラインも有しているうえ、業界注目度の高い製剤に関われるチャンスです!定年65歳まで長く働ける環境も整っているのも魅力です。ご興味がございましたら、是非お気軽にお問い合わせください。

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