Takeda

Lead CQV Compliance

India · Work style not stated · Full time

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About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerTakeda
LocationIndia
Work styleWork style not stated
Employment typeFull time
Employer posted29 Sep 2026

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

· Lead the CQV & Compliance Engineering discipline within the GCC and provide expertise supporting qualification readiness, compliance frameworks, and lifecycle quality strategies.

· Build and develop CQV and Compliance Engineering capabilities, talent, technical expertise, and succession pipelines within the GCC.

· Drive consistent application of risk-based CQV methodologies, standardized deliverables, digital qualification approaches and lifecycle-focused compliance practices.

Show full description

· Ensure engineering deliverables, qualification frameworks, and compliance processes support GMP, quality, regulatory, and business requirements.

Accountabilities

Leadership

Lead, coach, and develop CQV & Compliance Engineers.
Support recruitment, onboarding, succession planning, and capability development.
Manage discipline capacity, priorities, and resource allocation.

Qualification & Compliance Expertise

Provide expertise for qualification strategies, validation frameworks, and compliance methodologies.
Support qualification readiness reviews and compliance assessments.
Coordinate interfaces with Engineering, Quality, Manufacturing, Digital Manufacturing, and Project Teams.

Quality, Compliance & Governance

Ensure compliance with GMP requirements, Data Integrity principles, and Takeda standards.
Ensure alignment with ASTM E2500, GAMP5, CFR Part 11, and applicable regulatory requirements.
Lead discipline governance activities, risk assessments, quality reviews, and lessons learned.
Support inspection readiness and compliance initiatives.

Innovation & Continuous Improvement

Drive standardization and reuse of qualification and compliance frameworks.
Promote risk-based and digital qualification approaches.
Support continuous improvement of qualification and compliance methodologies.
Develop standards, templates, and best practices.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

Education

Bachelor's Degree in Engineering, Life Sciences, Pharmaceutical Sciences, Quality, or related discipline.
Master's Degree preferred.

Experience

10+ years of experience in CQV, Validation, Quality Engineering, Compliance, or related disciplines.
Experience supporting GMP-regulated facilities and capital projects.
Experience developing qualification frameworks, plans, and standards.
Experience leading technical teams and capability development initiatives.

Behavioural Competencies

Leadership and talent development.
Stakeholder management and collaboration.
Strategic thinking and decision making.
Quality and compliance mindset.
Continuous improvement mindset.
Strong communication and influencing skills.

Technical Skills

Qualification Planning and Strategy.
KNEAT and or other paperless validation system skills.
ASTM E2500 and Risk-Based Qualification.
Validation Framework Development.
GMP Compliance.
Data Integrity and Computerized Systems Compliance.
GAMP5 and CFR Part 11.
Inspection Readiness and Regulatory Expectations.
Engineering Quality Systems.

Locations

IND - Bengaluru

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

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