R&D Quality Laboratory Oversight (Associate Director)

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

OBJECTIVES/PURPOSE

• Provide global GxP Quality oversight of laboratory activities (method development, validation, release, stability) across modalities.
• Ensure implementation and execution of data integrity and quality system standards in internal and external laboratories.
• Partner with cross-functional teams to support analytical lifecycle management and regulatory submission readiness.
• Lead key quality initiatives and investigations related to laboratory operations.

ACCOUNTABILITIES

• Provide quality oversight for internal GxP and non-GxP laboratories performing analytical activities across the R&D pipeline.
• Review and approve GMP/GLP documentation including method validation protocols/reports, deviations, CAPAs, and audit responses.
• Ensure appropriate implementation of ALCOA+ principles and data integrity controls in laboratory systems and workflows.
• Lead or support laboratory-related investigations and inspections, ensuring timely root cause analysis and sustainable CAPA.
• Collaborate cross-functionally with Pharmaceutical Sciences, Regulatory Affairs, Manufacturing, and other Quality functions.
• Participate in the preparation and review of analytical sections for regulatory filings (IND/CTA/NDA/BLA).
• Contribute to the development and improvement of global procedures, standards, and quality frameworks for laboratory oversight.
• Monitor quality performance trends and proactively escalate compliance risks or improvement opportunities.

DIMENSIONS AND ASPECTS

Technical/Functional (Line) Expertise

• Strong understanding of GxP regulations, analytical methods, and laboratory operations across modalities (small molecules, biologics required; cell/gene therapy, plasma, or vaccines a plus).
• Demonstrated application of data integrity principles and computerized system controls in laboratory environments.
• Experience with internal and external laboratories, technical agreements, and audit preparation.
• Proficiency in quality risk management, deviation handling, and CAPA effectiveness.

Leadership

• Supports strategic goals of the R&D GMP Quality organization.
• Coaches junior team members or cross-functional partners on quality principles.
• Effectively communicates quality expectations and analytical requirements.
• Influences decision-making in cross-functional settings and supports change management efforts.

Decision-making and Autonomy

• Exercises judgment in resolving laboratory-related quality events and compliance issues.
• Makes independent decisions within the scope of analytical QA responsibilities.
• Provides recommendations for quality risk mitigation and system improvements.

Interaction

• Collaborates with Analytical Development, QC, Manufacturing, Regulatory, and QA teams.
• Interfaces with external laboratories and CMOs as required.
• Participates in regulatory inspections, audits, and governance meetings.

Innovation

• Contributes to process improvements and implementation of digital solutions.
• Promotes knowledge sharing and continuous improvement culture within the team.
• Identifies new tools or practices to enhance laboratory compliance and efficiency.

Complexity

• Supports laboratory oversight across a range of modalities and global sites.
• Navigates matrixed organizational structures and diverse cultural and regulatory landscapes.
• Balances scientific, compliance, and business needs in decision-making.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

• Bachelor's degree in Life Sciences, Chemistry, Biochemistry, or related field. Preffered advance degree (MS/PhD)
• 7+ years of relevant industry experience in quality oversight of laboratory operations
• Demonstrated experience in GMP/GLP, analytical testing, data integrity, and regulatory inspections
• Strong interpersonal, project management, and problem-solving skills
• Ability to operate in a global matrix environment and manage competing priorities

Employee Signature:

Date:

Manager Signature:

Date:

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

Worker Type

Worker Sub-Type

Time Type