Senior Principal Scientist API MST

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Job Description
The API Manufacturing Science & Technology (API MST) department provides technical solution to support Small Molecules and Oncology Operating Unit. This is a technical role in a rapidly growing pharmaceutical company where we use an outsourcing model for some of our manufacturing and testing activities. Products supported are primarily complex synthetic molecules.
About the role:
As Sr. Principal Scientist, you will be the primary technical point of contact for the API SMO OpU with external Contract Manufacturing Organizations (CMOs). The primary role will be to provide scientific and technical expertise for all drug substance related activities, ensuring that new and existing drug substance technology and related processes, procedures and specifications are transferred to our CMOs in a manner compliant with all regulatory and quality standards and to support cost-effective technical processes suitable for robust commercial production.
How you will contribute:
• New product introduction, New Chemical Entity process validation and CPV.• Technology selection and acquisition.• Process design, development, optimization and verification.• Technology transfer.• Continuous improvement.• Change Management.• Technical support and oversight of commercial API manufacturing.• Define capabilities required at the CMO to successfully support new product introduction and new chemical entity validation manufacture.• Assess gaps in capabilities and implements plan to build required capabilities at CMO to support technology transfer.• Partner with Pharmaceutical Sciences (PS) and Global Manufacturing Sciences (GMSci) in late-stage process development with technology selection, process design and optimization.• Design, develop and optimize product manufacturing process using robust DoE and QbD principles.• Author, review and approve relevant technical documentation, protocols,
reports and regulatory submissions including Process Risk and Safety,
Assessment, Technology Transfer Plan, Validation Master Plan etc.• Implement right first time (RFT) Technology Transfers and timing to business needs ensuring quality, costs and regulatory requirements.• Contribute and support due diligence activities for new product acquisition.• Assure proposed vendors are capable of passing regulatory inspections by the FDA or other government regulatory agencies. • Author and review regulatory documents for technical consistency and compliance for NDA and DMF etc. Provides responses to technical queries from the agencies.• Lead, prioritize and drive investigations to completion, using standardized approaches to timely closure to avoid product supply concerns. Ensures timeline for tasks are met and facilitates corrective action to maintain and where necessary maneuver timeline back on track.• Manages and maintains change controls throughout appropriate product groups• Develop and maintain technical product knowledge database and technical documents for assigned products. Dissects and interprets data from various sources, using the information to create scientific reports• Lead external CMO network to create or enhance capabilities to deliver RFT the needed quality and quantity of API.• Partner with CMOs to ensure quality of drug substance and drive elimination of customer complaints relating to API. Leads/participates in the deviation investigations, RCA and CAPA. • Build and maintain a network of robust relationships with regulators, CMOs, CROs and Key Opinion Leaders in their respective technical field.• Knowledge of the relevant cGMP, ICH and global Regulatory CMC guidance documents applicable to the function. Keep current on all issues that will affect the use of APIs (Regulatory, Stability etc).• In-depth knowledge of QbD, technology transfer, process development, scale up, optimization, DoE, PAT and risk assessment. • Demonstrated hands-on API plant manufacturing experience, technical proficiency, scientific creativity, and independent judgment. Proven track record for commercial process problem solving. • Able to serve as SME Author on CMC submissions. Support regulatory inspections and audits. • Able to effectively and independently develop, implement and manage multiple API projects that are global in nature.• Demonstrated ability to communicate successfully to present complex scientific information and develop credible relationships with a broad spectrum of people, including CMO's, Vendors / Suppliers and Colleagues.• On a routine basis interacts internally in person or remotely with individuals from Product Strategy, Quality, Compliance, External Supply Management, Pharm Science, GMSci, Regulatory Affairs and SMO OpU.

What you bring to Takeda:
• PhD in Organic Chemistry or Chemical Engineering with 10+ years or MS with 15+ years industry experience.• Hands-on experience in API process development, optimization and validation. • Direct experience in technology transfer and in supporting API manufacturing• Strong knowledge of synthetic organic chemistry and modern analytical methods Experience in global product launches and the associated CMC regulatory requirements.• Strong knowledge of cGMP/GLP regulations, ICH, FDA CMC Guidance Documents and DEA Regulations are preferred.• Recognized as an expert or leader in their specific field.• Strong technical, interpersonal, communication and leadership skills.
• Up to 20% domestic and international travel required.
Desired• Project Management Experience.• Six Sigma Certification
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:
Lexington, MA
U.S. Base Salary Range:
$169,400.00 - $266,200.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in 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, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
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
Lexington, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.