Analytical Development Director

5 days ago


Étreux, Hauts-de-France, United States Takeda Pharmaceutical Full time
Job Description

We are seeking a highly skilled and experienced Analytical Development Director - Late Stage to lead our analytical development team in the late stage. The successful candidate will be responsible for overseeing and managing late stage analytical development for clinical trial material efforts across three main areas.

The ideal candidate will have a strong background in analytical science, cGMP compliance, and CMC regulatory requirements. They will be able to drive decision-making within a cross-functional, cross-cultural global team structure and have experience with product development and clinical supply processes.

Key Responsibilities:

  • Develop and implement strategies to ensure timely and cost-effective delivery of high-quality products.
  • Collaborate with multiple functions within the Pharmaceutical Science organization to improve analytical, process, and product knowledge.
  • Contribute to overall functional direction globally and represent function within CMC/Pharmaceutical Science and across the global Takeda organization.

Requirements:

  • Master or PhD in chemistry, biology, pharmacy, or related pharmaceutical science.
  • At least 10 years relevant industry experience including significant experience in analytical science, cGMP compliance, and CMC regulatory requirements.
  • Leadership experience of teams including managers and scientists.

Salary: $190,000 - $230,000 per year.

Benefits: Medical, dental, vision insurance, 401(k) plan, company match, short-term and long-term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits.

Location: Boston, MA.



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