Director, Regulatory Affairs Vaccines CMC

Director, Regulatory Affairs Vaccines CMC

Vaccines prevent 2 to 3 million deaths each year and have transformed global public health. For the past 70 years, Takeda has supplied vaccines to protect the health of people in Japan. Today, Takeda's global vaccine business is applying innovation to tackle some of the world's most challenging infectious diseases, such as dengue, COVID-19, Zika and norovirus. Takeda’s team brings an outstanding track record and a wealth of knowledge in vaccine development, manufacturing and global access to advance a pipeline of vaccines to address some of the world's most pressing public health needs.
Job ID

R0120763

Date posted

04/16/2024

Location

Boston, Massachusetts
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’s Privacy Notice

and 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

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.
Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development. You will represent the vaccine regulatory affairs team on cross-functional Takeda Vaccines teams (commercial, clinical development, delivery, quality, etc.) to ensure that data are identified, obtained and effectively presented for the registration of products world-wide. The role requires strong focus on analytical, manufacturing, and facilities compliance.
You will also demonstrate leadership and comprehensive understanding of global vaccines CMC regulations and guidelines by applying interpersonal skills and expert Regulatory Affairs Vaccines (RAV) CMC knowledge to identify, communicate, address, and overcome challenges that arise during development and commercialization. You will successfully communicate and negotiate with international Health Authorities as necessary, directly and indirectly. As part of the RAV CMC team, you will report to the Head, RAV CMC and work with strategic partners globally.
How you will contribute:

Lead planning, execution, and management of regulatory submissions for assigned vaccines in various phases of clinical development, global marketing applications, and post-approval life cycle activities, as needed
Participate in technical development teams which require experienced interpretation of applicable EMA/FDA/ICH/Global regulations to ensure CMC compliance within the organization
Lead regulatory compliance assessment with respect to filing requirements for assigned vaccines throughout development and the commercial life cycle
Define CMC content (data and documentation) requirements for regulatory submissions and compile/review this content for conformance with established requirements
Represent Takeda RAV CMC in Health Authority meetings and lead or supports CMC preparation activities for meetings with Health Authorities on CMC related matters
Interact directly with international Health Authorities, as required. Participate in and/or lead agency meetings on CMC topics.
Ensure project team colleagues, line management, and key stakeholders are apprised of risks that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner
Stay abreast of current and evolving regulatory CMC requirements, apply this knowledge to assigned projects, and share knowledge and experience with others to support their development
May serve as direct/matrix manager of RAV CMC staff, depending on project. Responsible for prioritization of workload and professional development of staff where applicable.
Minimum Requirements/Qualifications:

BS/BA Degree in a scientific/engineering discipline required, Advanced Degree preferred.
At least 10 years Regulatory CMC experience (vaccines or biologics experience required). Alternatively 5 years Regulatory CMC experience combined with 5 years relevant vaccines or biologics experience (e.g. Pharmaceutical Development, Process Development, Analytical Development, Production, Quality Assurance). Experience with managing BLA/MAA content and format required.
Experience with regulatory registration of biological drug substances or drug products (including sterile parenteral dosage forms) is required.
Excellent written and oral communication skills required.
Demonstrated track record of successful interactions with US FDA, European Agencies and, preferably, other global health authorities related to CMC submissions.
Understanding of scientific principles and regulatory CMC requirements relevant to global vaccine development, registration, and post-market support. Proven ability to provide strategic regulatory guidance to teams.
Demonstrated ability to deal with issues of critical importance, provide regulatory advice and experience with developing reasoned decisions on regulatory issues for which there may not be clear/specific regulatory guidance.
Demonstrated leadership, problem-solving ability, flexibility and teamwork
Exercises good judgement in elevating and communicating actual or potential regulatory risks to teams and line management.
Active participation in Agency/Industry groups/forums preferred.
Some international travel may be required.
What Takeda can offer you:

401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs
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" in accordance with Takeda's Hybrid and Remote Work policy.
#RM-LI
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, MA

U.S. Base Salary Range:
$169,400.00 - $266,200.00

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’s Privacy Notice

and 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

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.
Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development. You will represent the vaccine regulatory affairs team on cross-functional Takeda Vaccines teams (commercial, clinical development, delivery, quality, etc.) to ensure that data are identified, obtained and effectively presented for the registration of products world-wide. The role requires strong focus on analytical, manufacturing, and facilities compliance.
You will also demonstrate leadership and comprehensive understanding of global vaccines CMC regulations and guidelines by applying interpersonal skills and expert Regulatory Affairs Vaccines (RAV) CMC knowledge to identify, communicate, address, and overcome challenges that arise during development and commercialization. You will successfully communicate and negotiate with international Health Authorities as necessary, directly and indirectly. As part of the RAV CMC team, you will report to the Head, RAV CMC and work with strategic partners globally.
How you will contribute:

Lead planning, execution, and management of regulatory submissions for assigned vaccines in various phases of clinical development, global marketing applications, and post-approval life cycle activities, as needed
Participate in technical development teams which require experienced interpretation of applicable EMA/FDA/ICH/Global regulations to ensure CMC compliance within the organization
Lead regulatory compliance assessment with respect to filing requirements for assigned vaccines throughout development and the commercial life cycle
Define CMC content (data and documentation) requirements for regulatory submissions and compile/review this content for conformance with established requirements
Represent Takeda RAV CMC in Health Authority meetings and lead or supports CMC preparation activities for meetings with Health Authorities on CMC related matters
Interact directly with international Health Authorities, as required. Participate in and/or lead agency meetings on CMC topics.
Ensure project team colleagues, line management, and key stakeholders are apprised of risks that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner
Stay abreast of current and evolving regulatory CMC requirements, apply this knowledge to assigned projects, and share knowledge and experience with others to support their development
May serve as direct/matrix manager of RAV CMC staff, depending on project. Responsible for prioritization of workload and professional development of staff where applicable.
Minimum Requirements/Qualifications:

BS/BA Degree in a scientific/engineering discipline required, Advanced Degree preferred.
At least 10 years Regulatory CMC experience (vaccines or biologics experience required). Alternatively 5 years Regulatory CMC experience combined with 5 years relevant vaccines or biologics experience (e.g. Pharmaceutical Development, Process Development, Analytical Development, Production, Quality Assurance). Experience with managing BLA/MAA content and format required.
Experience with regulatory registration of biological drug substances or drug products (including sterile parenteral dosage forms) is required.
Excellent written and oral communication skills required.
Demonstrated track record of successful interactions with US FDA, European Agencies and, preferably, other global health authorities related to CMC submissions.
Understanding of scientific principles and regulatory CMC requirements relevant to global vaccine development, registration, and post-market support. Proven ability to provide strategic regulatory guidance to teams.
Demonstrated ability to deal with issues of critical importance, provide regulatory advice and experience with developing reasoned decisions on regulatory issues for which there may not be clear/specific regulatory guidance.
Demonstrated leadership, problem-solving ability, flexibility and teamwork
Exercises good judgement in elevating and communicating actual or potential regulatory risks to teams and line management.
Active participation in Agency/Industry groups/forums preferred.
Some international travel may be required.
What Takeda can offer you:

401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs
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" in accordance with Takeda's Hybrid and Remote Work policy.
#RM-LI
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, 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

e

mployee

s

may be eligible for

s

hort

-

t

erm and/

or

l

ong-

t

erm

incentive

s

.

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, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
What makes a successful team member within Vaccines at Takeda?
Integrity
Inventive
Perseverance
Vaccines represent a new dimension of global impact — successful leadership at Takeda can be encompassed in these four pillars:
Demonstrating

strategic enterprise thinking, finding innovative ways to serve patients and build trust, reputation and business
Creating

the environment that inspires and enables people to move the organization forward
Focusing

on the few priorities and delivers superior results
Elevating

the capabilities of the organization for now and the future
Inclusion
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.
Top Workplace
Top Workplace
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
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.
Empowerment
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

Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
Planet
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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