
Senior Associate – Specialist, Global Regulatory Affairs CMC
Boston, Massachusetts- Job Level: Senior
- Travel: Minimal (if any)
Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.
In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.
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Job Description
About the role:
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
Senior Associate – Specialist, Global Regulatory Affairs CMC role is within in the GRA Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows:
With supervision, support the execution of regulatory CMC investigational, registration and post-approval strategies for assigned products.
Support RA CMC member on Regulatory, Pharmaceutical Development, and Commercial project teams throughout clinical development and commercial lifecycle.
With supervision, prepare project plans and timelines for CMC submission activities and responsible for organization of CMC-relateddocuments for regulatorysubmissions.
Expected to have a sound understanding of global RA CMC regulations and guidelines and participate in the development of strategies to enhanceprobability of regulatory success or enhancingregulatory compliance. Has ability to applythisunderstanding to support the development and execution of strategies to enhanceprobability of regulatory success and regulatory compliance.
Sound analytical or processunderstandingthatenables the development of robust and accurate submissions.
Assist in the coordination of communication and collaborationamonginternal and externalcolleagues.
Minimum Requirements/Qualifications:
PhD / PharmD, or MS/BS with 3+ years of relevant pharmaceutical experience(RegulatoryCMC,Pharmaceutical Development, Analytical Development, GMP Manufacturing, Quality Assurance, etc.)
Understanding of scientificprinciplesrelevant to global drugdevelopment and post-market support.
Ability to understand and communicateregulatory strategy to drugdevelopment, registration, and post-market support teams.
Analyzeissues with attention to detail.
Ability to assess alternative approaches.
Base regulatory strategy recommendations on precedents and otherregulatory intelligence aswellasregulations and guidelines.
Exercises good judgement in elevating and communicatingactual or potentialissues to line management.
Understandswhoisresponsible for differentdecisions and escalatesasnecessary
Support to applydecisionstaken by the company
Demonstrates sound understanding and knowledge of the principles, practices and processeswithin the GRA organization and with key stakeholder groups.
Consistentlydemonstrates a “can do” attitudewhichresults in otherswillingness to work together to drive results.
Demonstratesawareness of company's mission, culture, functions, policies and procedures to operate effectively
Proactivelyestablishesrelationships to accomplishindividualobjectives
Demonstratesattention to detail and problem-solving abilities
Good judgement in elevating and communicatingactual or potentialissues to line management.
Excellentwritten and oralcommunication skills.
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
This position is currently classified as "hybrid" following Takeda's Hybrid and Remote Work policy.
#LI-Hybrid
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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:
Boston, MAU.S. Base Salary Range:
$99,500.00 - $156,420.00The 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-termincentives. 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
Boston, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeJob Exempt
YesIt 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.The heart of our work
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Working at Takeda
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Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team. -
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission. -
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients. -
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Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2024. -
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. -
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
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Create an exceptional people experience.
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