Head, Analytical Development Synthetic Molecules – Late Stage (Sr. Director)

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’sPrivacy Noticeand 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: 

• Lead and develop a global team of managers and scientists and their teams in the field of analytical development in the field of late stage synthetic molecules

• Oversee and manage late stage analytical development for clinical trial material efforts across three main areas: a) Characterization and in vitro comparability, b) Method development and validation of methods for release/stability use, c) Method development for In-Process analytics

• Contribute to product development and transfer from development to commercialization by collaborating 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.

• Implement and execute externalization activities with external partners, facilitate development of execution plans for each, and ensure completion of agreed upon activities

ACCOUNTABILITIES:

• Direct and indirect supervisory responsibilities in analytical areas for development of high-quality late stage synthetic molecules therapeutics (small molecules, oligonucleotides, …)

• Drive global late stage team to obtain scientific data; data compilation and review; preparation and review of technical reports, global regulatory filings, and other documentation; project/CMC team representation/leadership; technical interactions with internal partners and contract laboratories

• Collaborate with other functions in Pharmaceutical Sciences to encourage strategic alignment and successful achievement of shared goals

• Be well versed in all stages of analytical development and understand the global regulatory trends for CMC activities, to ensure robust and high-quality regulatory filings in all major countries

• Develop, implement and execute a smart sourcing strategy

• Lead global CMC key initiatives and represent Pharmaceutical Science to other cross functional stakeholder key initiatives

• Manage functional area budget and human resources to be within required limits

• Drive continuous improvement in the technology, methodology and business processes used to support analytical development, characterization and associated operational and documentation systems

• Strong knowledge of ICH and other regulatory guidelines including Quality by Design

• Maintain an active understanding of the future trends of medicine to build an organization adaptable for the future

• Inspire confidence in team members and lead the organization culture, promoting a healthy and inclusive working environment

• Build future leadership while mentoring direct reports and junior employees

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

• 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, CMC regulatory requirements in multiple analytical development areas

• Leadership experience of teams including managers and scientists. Development of team members to managers of scientific analytical teams including individual contributors with an exceptional commitment to science

• Direct experience in analytical development for synthetic molecules, especially late stage assets, and ability to drive study completion in a timely, sustainable, robust and cost-efficient manner

• Drive decision making within a cross-functional, cross-cultural global team structure

• Knowledge and experience with product development and clinical supply processes and product commercialization. Quality experience is of advantage

• Experience in reviewing and approving analytical-related CMC sections of IND/IMPD and BLA/MAA regulatory submissions. Knowledgeable in European, Japanese, Chinese and US CMC regulatory requirements for Biologics

• Develop, implement and execute a smart sourcing strategy

• Deep and broad knowledge of analytical chemistry of synthetic molecules in support of drug substance and drug product release and stability method development, raw material control, in process control, and characterization

• Exceptional problem solving and troubleshooting skills related to analytical methodology

• Proven working knowledge of current GMPs, ICH guidelines including Quality by Design, other regulatory requirements, and various quality system

• Proven knowledge, skills, and abilities with statistical analysis (with emphasis on analytical testing applications).

• Knowledge of complex and state-of-the-art methodology for biologics GMP method development and characterization

• Proven ability to work efficiently and effectively as a leader of managers and scientists

• OPEX and CAPEX budget planning and controlling skills and efficient resource planning

• Strong verbal, presentation, and written communication skills.  Can concisely articulate and deliver effective presentations on complex technical issues to non-technical audience.

• Ability to create collaborative and trusting relationships internally and with external partners.

• Requires strong organizational skills and attention to detail for composing and proofing materials, scheduling, establishing priorities, and meeting deadlines.

• Other professional competencies include: building authentic relationship, global and cross-boundary communication, excellence in execution, courage to challenge, inspiring and motivating others

TRAVEL REQUIREMENTS:

• Approximately 10-15% travel is required, including domestic and international flights with overnight stays

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

U.S. Base Salary Range:

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 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.

Locations

Worker Type

Worker Sub-Type

Time Type

Job Exempt