Associate Director or Principal Scientist, Facility Operations, Pharmaceuti at Takeda Pharmaceuticals

Fujisawa, , Japan -

Full Time

Start Date

Immediate

Expiry Date

28 Jul, 26

Salary

0.0

Posted On

29 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP manufacturing, Biologics, Sterile drug products, Facility maintenance, Plant engineering, Regulatory compliance, Strategic planning, Team leadership, Project management, Construction management, Budget management, Japanese language proficiency, Risk management, Quality assurance, Stakeholder management

Industry

Pharmaceutical Manufacturing

Description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Please note this job requires business level Japanese in speaking, writing, and reading. タケダの紹介タケダは「世界中の人々の健康と輝かしい未来に貢献する」ことを企業の存在意義（パーパス）としています。そして目指す未来を共有しながら、一人ひとりが自分の可能性を引き出し、お互いの個性を認め合う、多様性にあふれた先進的な組織作りに取り組んでいます。私たちと一緒に、世界中の人々のいのちに貢献し、さらなる成長と活躍を目指しませんか。タケダはグローバルな研究開発型のバイオ医薬品のリーディングカンパニーです。従業員は創業時から受け継いできたタケダの価値観であるタケダイズム（誠実＝公正・正直・不屈）を道しるべとしながら、患者さんに寄り添い（Patient）人々と信頼関係を築き（Trust）社会的評価を向上させ（Reputation）持続可能な事業を発展させる（Business）を日々の行動指針としています。 Objective / Purpose: This position is responsible for GMP manufacturing of biologics drug substances (DS) and sterile drug products (DP) for clinical trials, and for their in-process and release testing, in compliance with cGMP, as the Maintenance Director for Facilities Control. Manage the schedule of GMP manufacturing/testing of biologics DS and DP (in the future) and regular maintenance. Establish efficient and robust strategy of engineering and maintenance. Executes strategic planning and operations in the scheme of facilities control. Develops biologics and sterile manufacturing technologies with the improvement of manufacturing efficiency using advanced facility-related technologies including new facility/equipment installation. Manage budget for new equipment implementations and maintenance operations. Management and training of outsourced contractors. Accountabilities: HR Management: Ensuring proper training, qualifications and continuous professional development. Provides strategic direction and oversight to staff to fulfill the following accountabilities. Leads to carry out cGMP compliant maintenance on site, manufacturing and testing operations to reduce the risk of deviations from armed regulatory requirements and promote continuous improvement. Builds and leads efficient and robust maintenance program to ensure stable manufacturing and testing. Continues to evaluate and study innovative facilities and equipment technologies, and to contribute constantly evolving biologics and sterile manufacturing technologies focusing on cutting edge sciences and technologies. Builds good relationships with internal (BPD, AD, DPDD, PS quality, EHS etc.) and external stakeholders (Contractors, Vendors etc.) to carry out facility maintenance, GMP manufacturing, testing operations and manufacturing technology development Establish and maintain safety working environment. Education & Competencies : Majored or worked in the field of Pharmacy, Chemistry, Biology, Engineering or related field. Minimum of 5 years of increasingly responsibility and experience in pharmaceutical industry. Minimum of 3 years of experience for GMP manufacturing or maintenance including 1 year experience of construction work management or maintenance work management on-site. Having experiences for biologics or sterile production is preferred. In-depth knowledge of any field related to plant engineering, such as architecture, electricity, machinery, piping, instrument, etc. In depth knowledge of current relevant international regulatory requirements and guidance for the pharmaceutical industry. Demonstrated ability to anticipate issues and manage a team to proactively implement solutions. Excellent organizational and communication skills. Has the ability to influence at all levels of the organization. Demonstrated ability to negotiate difficult issues and arrive at mutually beneficial solutions. Ability to analyze a wide variety of information and data to make management decisions. regarding potential risks associated with product quality and regulatory compliance. Demonstrated ability to effectively lead and motivate a team of direct reports, build on strengths, and address areas for improvement. In depth knowledge of manufacturing, testing facilities and equipment. Fluent Japanese communication skill is mandatory and English communication skill is proffered. Takeda Compensation and Benefits Summary: Allowances: Commutation, Housing, Overtime Work etc. Salary Increase: Annually, Bonus Payment: Twice a year Working Hours: Headquarters (Osaka/ Tokyo) 9:00-17:30, Production Sites (Osaka/ Yamaguchi) 8:00-16:45, (Narita) 8:30-17:15, Research Site (Kanagawa) 9:00-17:45 Holidays: Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year) Paid Leaves: Annual Paid Leave, Special Paid Leave, Sick Leave, Family Support Leave, Maternity Leave, Childcare Leave, Family Nursing Leave. Flexible Work Styles: Flextime, Telework Benefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc. Important Notice concerning working conditions: It is possible the job scope may change at the company’s discretion. It is possible the department and workplace may change at the company’s discretion. Locations Fujisawa, Japan Worker Type Employee Worker Sub-Type Regular Time Type Full time Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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Responsibilities

This position oversees GMP manufacturing and facility maintenance for biologics and sterile drug products to ensure regulatory compliance and operational efficiency. The role involves strategic planning, budget management, and leading teams to implement innovative facility technologies.