Job Description

Associate Director, Global Regulatory Affairs GI & Inflammation

Apply for the role at TakedaPharmaceutical Nordics AB.

Job Description

Associate Director responsible for regulatory affairs for GI & Inflammation programs. Provides strategic and tactical advice, leads crossfunctional initiatives, and maintains compliance with regulatory requirements.

Accountabilities

• Lead global regulatory strategies for complex or highly complex projects.
• Define and execute global regulatory strategies and provide tactical guidance.
• Represent Global Regulatory Teams at project meetings and maintain regulatory compliance.
• Establish and manage relationships with health authorities, including FDA meetings.
• Accountable for all US FDA submissions related to assigned projects.
• Oversee vendor responsibility for regulatory activities.
• Partner with market access for value evidence topics.
• Demonstrate Takeda leadership behaviors.

Education & Competencies

• Bachelors Degree in a scientific discipline (PharmD/PhD/MD strongly preferred).
• 6+ years of pharmaceutical industry experience, including 4+ years regulatory experience.
• Preferred experience in reviewing, authoring, or managing components of regulatory submissions.
• Solid knowledge of drug development process and regulatory requirements (FDA, EU, Canada, ROW).
• Strong oral and written communication skills and negotiation ability.
• Proactive riskmitigation and strategic regulatory solution development.
• Team collaboration and global team alignment.

Hybrid Statement

This position is classified as hybrid in accordance with Takedas Hybrid and Remote Work policy.

Compensation and Benefits Summary

Location: Boston, MA

Base Salary Range: $153,600.00 $241,340.00

U.S. based employees may be eligible for shortterm and longterm incentives. Benefits include medical, dental, vision, 401(k) with match, shortterm and longterm disability, life insurance, tuition reimbursement, volunteer time off, company holidays, and wellbeing benefits. Paid vacation up to 120 hours and sick time up to 80 hours per year.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, veteran status, or other protected characteristic.

Job Details

Job Exempt: Yes

Job Function: Legal

Industry: Pharmaceutical Manufacturing

Worker Type: Employee

Time Type: Full time

Seniority Level: Director

Employment Type: Fulltime

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