Senior Associate Director, Global Regulatory Labeling and Compliance
3 weeks ago
About the Role
">We are seeking a highly skilled Senior Associate Director, Global Regulatory Labeling and Compliance to join our team at Takeda Pharmaceutical. This role will be responsible for leading global labeling compliance and quality initiatives, ensuring alignment with regulatory requirements and industry best practices.
About Us
">Takeda is a global pharmaceutical company dedicated to bringing better health to people and a brighter future to the world. We are committed 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 or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Key Responsibilities
">- Lead cross-functional teams and deliver results in a matrix organization.
- Develop and implement processes for end-to-end tracking of global labeling updates.
- Collaborate with internal stakeholders and external partners on labeling compliance and quality initiatives.
- Ensure compliance with legislation and regulations related to labeling and regulatory affairs.
- Represent Takeda at industry forums and conferences.
Requirements
">- Bachelor's degree (or equivalent) required; Master's preferred.
- 8+ years of experience in pharmaceutical industry, with good exposure to Regulatory Affairs, labeling, quality assurance, and/or compliance.
- Familiarity with inspections and audit procedures.
- Strong knowledge of business area and interactions with strong regulatory environment and ability to identify and proactively manage the interactions necessary for achieving business goals and objectives.
- Able to manage both time and priority constraints and to manage multiple priorities simultaneously.
- Capability to critically analyze complex and/or ambiguous information and the impact on products and process and to effectively communicate complex issues both verbally and in writing.
Salary and Benefits
">The estimated salary range for this position is $125,000 - $155,000 per year, depending on qualifications and experience. U.S. based employees may be eligible for short-term and/or long-term incentives, medical, dental, vision insurance, 401(k) plan, short-term and long-term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others.
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Allentown, Pennsylvania, United States Takeda Pharmaceutical Full timeJob Summary:Takeda Pharmaceutical is seeking an experienced Associate Director to lead our global regulatory affairs labeling compliance efforts. The ideal candidate will have a strong background in pharmaceutical regulations, labeling, and quality assurance, with excellent analytical, technical, and problem-solving skills.About the Role:This role involves...
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Allentown, Pennsylvania, United States Takeda Pharmaceutical Full time**Job Overview**Takeda Pharmaceutical is seeking an experienced Associate Director to lead our Global Regulatory Affairs Labeling Compliance team. This role will be responsible for ensuring regulatory approval for new products and product amendments, while maintaining license currency and compliance with legislation and regulations.Key...
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