Global Pharmaceutical Science Director
1 month ago
We are seeking an experienced Global Pharmaceutical Science Director to lead our team in the field of analytical controls and compliance. As a key member of our organization, you will be responsible for developing and implementing strategies to control quality of drug substances and products based on current Good Laboratory/Manufacturing Practice (cGMP, cGLP) regulations.
About UsTakeda Pharmaceutical is committed to creating a diverse workforce and providing equal employment opportunities to all employees and applicants 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.
About the JobThis role offers a unique opportunity to contribute to product development from Research to Commercialization by collaborating with multiple functions within the Pharmaceutical Science organization to improve analytical, process and product knowledge. You will also have the chance to develop and implement externalization activities with external partners, facilitate development of execution plans for each, and ensure completion of agreed upon activities.
Key Responsibilities:- Lead and develop a global team of managers and scientists and their teams in the field of analytical controls and compliance
- Develop and manage strategies for regional and global departmental infrastructure, resources, projects, etc. in conjunction with senior staff and global line and function heads
- Analyze and synthesize concepts from diverse information –and articulate them effectively
- Contribute to overall functional direction globally and represent function within CMC/Pharmaceutical Science and across the global Takeda organization
- Bachelor degree with 20+ years of experience
- Advanced degree with 15+ years relevant industry experience
- Minimum of 10 years of experience working in CMC analytical development area for active pharmaceutical ingredients and drug products under cGMP's
- Demonstrates effective project management skills
- GMP and compliance experience required
- Analytical method development experience required
- Regulatory submission experience required with basic knowledge for regulatory guidelines
- Familiarity with working in a global setting
The estimated salary range for this position is $150,000 - $200,000 per year, depending on qualifications and experience. Additionally, U.S.-based employees may be eligible for short-term and/or long-term incentives, medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits.
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