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Associate Director Process Engineering
| 採用企業 | 武田薬品工業株式会社 |
| 勤務地 | 神奈川県 |
| 雇用形態 | 正社員 |
| 給与 | 700万円 ~ 1600万円 |
募集要項
【求人No NJB2186970】
Job Description
Synthetic Molecule Process Development （SMPD） is responsible for the development of robust sustainable and cost effective processes for the manufacture of new synthetic molecule pharmaceuticals along with methods for achieving and controlling high standards of purity and quality.
The successful candidate will be responsible for leading a group of Engineers responsible for all aspects of reaction particle engineering including the development of scale down models for the study of unit operations process safety evaluation as well as technical transfer to external contract manufacturing organizations.
The successful candidate will be recognized as a technical resource/expert within SMPD and across Pharmaceutical Sciences and utilize his/ her technical expertise to contribute across multiple projects and drive technical/scientific strategy.
The Associate Director will be collaborating closely with the Chemistry and Technology groups to apply enabling emerging development and manufacturing technologies and will be responsible for helping shape the department’s technology roadmap based on pipeline needs and current trends in research.
The successful candidate will be responsible for maintaining and growing the department’s strategic relationships with our outsourcing partners as well as directing and managing outsourcing across a product platform as appropriate.
応募必要条件
| 職務経験 | 無し |
| キャリアレベル | 中途経験者レベル |
| 英語レベル | ビジネス会話レベル |
| 日本語レベル | ネイティブ |
| 最終学歴 | 大学卒： 学士号 |
| 現在のビザ | 日本での就労許可が必要です |
スキル・資格
※英文レジュメが必要となります※ The ideal candidate will have deep experience in using process analytical technologies （PAT） in combination with mathematical models （both statistical first principle） to enhance process understanding to effectively develop/ optimize/ scale up and troubleshoot processes. strive to continuously improve how pipeline projects are supported and will be developing new workflows to facilitate and accelerate process development optimization and understanding as well as technical transfer to manufacturing leveraging digital tools automation robotics and/ or cobotics. Education and Experience: A Ph.D. degree with 3+ years of academic post doctoral or pharmaceutical industry experience; an MS degree with 9+ years of pharmaceutical industry experience; or a BS degree with 11+ years of pharmaceutical industry experience. Degrees in chemical engineering required. Experience in the use of mathematical both statistical and first principle models as well as advanced process control systems preferred Experience in building reaction kinetic models as well as process models preferred. Experience in building laboratory and pilot plant equipment a plus Experience in crystallization process development and scale up with an emphasis on form purity and particle size control a plus Experience in the use and scale up of milling technologies （both dry and wet） for particle size control a plus Experience in the use of process analytical technologies （FT IR NIR FBRM UV vis etc.） required Experience in building chemometric models preferred Experience in developing continuous processes a plus Sound knowledge of current Good Manufacturing Practices （cGMP） preferred Experience working in a pilot plant a plus Previous experience with the use of contract facilities and managing technical transfers a plus Experience in working in a multi disciplinary team environment Proven scientific track record through presentations at scientific conferences and publication of pier reviewed manuscripts Knowledge and Skills: Analytical and Problem Solving Skills Able to troubleshoot critical issues or problems using appropriate information and determine causes and possible solutions Teamwork Ability to work well on global cross functional teams. Communication Skills Able to expresses one’s self clearly and concisely within team; documents issues and/or concerns concisely with colleagues; adjusts communication style as appropriate for the audience; timely and effectively communicates with senior management; technical writing skills to support authorship and approval of internal technical documents Organization ・ Exercises good time management and prioritization skills to balance multiple project and departmental objectives Technical Subject matter expertise in a specific scientific area or areas. Knowledge Sharing Ability to capture knowledge within the organization; improves solutions processes and deliverables through use of information; improves information capital by contributing experience theories deliverables and models for others to use Resource Management Project management skills; ability to manage one’s time within individual departmental External Involvement ・ Demonstrated involvement in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events. Interacts with external vendors for projects Leadership Skills ・ Develops and uses knowledge and interpersonal skills to appropriately influence and guide others towards the accomplishment of department/function goals and objectives.勤務地
- 神奈川県
労働条件
| 雇用形態 | 正社員 |
| 給与 | 700万円 ~ 1600万円 |
| 勤務時間 | 09:00 ～ 17:45 |
| 休日・休暇 | 【有給休暇】有給休暇は入社後4ヶ月目から付与されます 初年度 12日 4か月目から 【休日】完全週休二日制 土 日 祝日 年末… |
| 業種 | 医薬品 |
職種
- 技術系（電気・電子・半導体） > 設計・開発エンジニア
- 技術系（機械・メカトロ・自動車） > 生産管理・品質管理・品質保証・工場長（機械・自動車）
- 技術・専門職系（メディカル） > 薬事・学術
