Takeda Pharmaceuticals
Head RDQCS Compliance
Takeda Pharmaceuticals, Boston, Massachusetts, us, 02298
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
Job Title : Head RDQCS ComplianceLocation : Cambridge, MAAbout the role:
Leads the global R&D Quality Compliance organization, providing oversight of the quality systems supporting Takeda’s R&D Quality organization across the RDQ enterprise and ensuring that it is robust, aligned with, and compliant to applicable regulatory requirements, and governed and positioned for continual improvement.Establishes the framework for quality oversight of the R&D Quality Management System.
Serves as a strategic Quality Partner to Compliance leads across R&D Quality and the Enterprise Global Quality organization.
Key member of the RDQCS Leadership Team, contributing to the design, implementation and advancement of the R&D Quality Management System strategy, model and operations.
How you will contribute:
Responsible for the RDQ framework of audit and inspection management, inspection readiness, gap assessments, risk management and incident escalation. Builds strategic plans for R&D audit programs and inspection preparation to minimize critical observations and ensure Takeda’s regulatory reputation remains positive with global authorities in coordination with R&D Quality leadership.
Leads the systematic application of Risk Management principles across RDQ, ensuring consistency of approach and compliance to SOPs. Responsible for authoring, editing, and circulating for approval the associated family of documents.
Owner of the RDQ Regulatory Intelligence program, reviewing, documenting and gap assessing global regulatory changes across all GxPs (GMP, GCP, GDP, GLP, PV) used within R&D/R&D Quality to ensure continued compliance with current global regulations.
Accountable for strategic oversight of the application of the gap assessment process, ensuring consistency of approach and compliance to SOPs. Responsible for identifying and executing on process improvements that are identified associated with the process.
Leads the R&D Quality Compliance team in stewardship of the R&D Quality Management System, ensuring R&D and R&D Quality remain in compliance with Global GxP regulations.
Leads representatives from across R&D/R&D Quality those who serve as system owners for centrally accessed QMS processes Advances R&D/RDQ-wide forums to increase awareness, foster cross-functional learning, and improve knowledge. Works with system owners to develop metrics, trending programs, and continuous improvement plans for processes and systems used across R&D/R&D Quality.
Define, lead, and implement critical projects which enhance RDQ’s efficiencies and innovation. Engage in global, enterprise-wide cross-functional project and programs on behalf of RDQ to serve key business partners in R&D/R&D Quality.
Provides subject matter expertise and consultation for R&D Compliance related to deviations, CAPAs, change controls, responses to inspection outcomes and incident escalations. Escalates issues and incidents with regulatory authorities in coordination with R&D and R&D Quality leadership.
What you bring to Takeda:
Bachelor’s Degree in Chemistry, Biology, Engineering, or related field.
Minimum of 10 years professional working experience in the field of healthcare products or related activitiessuch aspharmaceuticalor devicemanufacturing, Quality Control or Quality Assurance including at least 4 years in GMP Quality or Compliance.
Six sigma/lean processing, project management professional and/or auditor certification preferred
Technical/Functional (Line) ExpertiseWorking knowledge of current GxP (e.g,, Good Manufacturing Practice, Good Laboratory Practices, Good Clinical Practices, Pharmacovigilance) requirements for the pharmaceutical industry
Experience in compliance and systems related processes and tasks
Experience with risk management strategies and general project management
Proven success in identifying and implementing continuous improvement initiatives
Proficient in analyzing data to identify performance trends
Ability to proactively manage the development and re-engineering of key processes and systems in support of the business’s mission
LeadershipDemonstrated teamwork, initiative, and problem-solving skills
Clear, concise, and consistent in written and verbal communications
High attention to detail
Decision-making and AutonomyAble to manage projects, programs and tasks with little, to no, oversight. Able to analyze data and make recommendations to management and/or escalate as appropriate.
InteractionExperience working within complex/matrixed organizations
Demonstrated ability to collaborate with and achieve results through others, the ability to build strong and sustainable relationships and the capability to interact within all levels of the organization
InnovationAbility to read, analyze and interpret common scientific and technical data/reports and legal/regulatory documents
Effectively presents information to management, internal groups, and stakeholders
ComplexityAnalytical capabilities with the ability to analyze a wide variety of information and data to determine potential risks
Ability to anticipate potential problems and risks related to quality expectations and regulatory compliance, formulate action plans, and implement solutions
Ability to work effectively in a fast paced, rapidly changing environment and to work on multiple work streams and projects simultaneously
Important Considerations
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection.
Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
Work in a cold, wet environment.
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
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.#GMSGQ #ZR1 #LI-MA1Takeda Compensation and Benefits SummaryWe 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 StatementTakeda 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
Job ExemptYes#J-18808-Ljbffr
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
Job Title : Head RDQCS ComplianceLocation : Cambridge, MAAbout the role:
Leads the global R&D Quality Compliance organization, providing oversight of the quality systems supporting Takeda’s R&D Quality organization across the RDQ enterprise and ensuring that it is robust, aligned with, and compliant to applicable regulatory requirements, and governed and positioned for continual improvement.Establishes the framework for quality oversight of the R&D Quality Management System.
Serves as a strategic Quality Partner to Compliance leads across R&D Quality and the Enterprise Global Quality organization.
Key member of the RDQCS Leadership Team, contributing to the design, implementation and advancement of the R&D Quality Management System strategy, model and operations.
How you will contribute:
Responsible for the RDQ framework of audit and inspection management, inspection readiness, gap assessments, risk management and incident escalation. Builds strategic plans for R&D audit programs and inspection preparation to minimize critical observations and ensure Takeda’s regulatory reputation remains positive with global authorities in coordination with R&D Quality leadership.
Leads the systematic application of Risk Management principles across RDQ, ensuring consistency of approach and compliance to SOPs. Responsible for authoring, editing, and circulating for approval the associated family of documents.
Owner of the RDQ Regulatory Intelligence program, reviewing, documenting and gap assessing global regulatory changes across all GxPs (GMP, GCP, GDP, GLP, PV) used within R&D/R&D Quality to ensure continued compliance with current global regulations.
Accountable for strategic oversight of the application of the gap assessment process, ensuring consistency of approach and compliance to SOPs. Responsible for identifying and executing on process improvements that are identified associated with the process.
Leads the R&D Quality Compliance team in stewardship of the R&D Quality Management System, ensuring R&D and R&D Quality remain in compliance with Global GxP regulations.
Leads representatives from across R&D/R&D Quality those who serve as system owners for centrally accessed QMS processes Advances R&D/RDQ-wide forums to increase awareness, foster cross-functional learning, and improve knowledge. Works with system owners to develop metrics, trending programs, and continuous improvement plans for processes and systems used across R&D/R&D Quality.
Define, lead, and implement critical projects which enhance RDQ’s efficiencies and innovation. Engage in global, enterprise-wide cross-functional project and programs on behalf of RDQ to serve key business partners in R&D/R&D Quality.
Provides subject matter expertise and consultation for R&D Compliance related to deviations, CAPAs, change controls, responses to inspection outcomes and incident escalations. Escalates issues and incidents with regulatory authorities in coordination with R&D and R&D Quality leadership.
What you bring to Takeda:
Bachelor’s Degree in Chemistry, Biology, Engineering, or related field.
Minimum of 10 years professional working experience in the field of healthcare products or related activitiessuch aspharmaceuticalor devicemanufacturing, Quality Control or Quality Assurance including at least 4 years in GMP Quality or Compliance.
Six sigma/lean processing, project management professional and/or auditor certification preferred
Technical/Functional (Line) ExpertiseWorking knowledge of current GxP (e.g,, Good Manufacturing Practice, Good Laboratory Practices, Good Clinical Practices, Pharmacovigilance) requirements for the pharmaceutical industry
Experience in compliance and systems related processes and tasks
Experience with risk management strategies and general project management
Proven success in identifying and implementing continuous improvement initiatives
Proficient in analyzing data to identify performance trends
Ability to proactively manage the development and re-engineering of key processes and systems in support of the business’s mission
LeadershipDemonstrated teamwork, initiative, and problem-solving skills
Clear, concise, and consistent in written and verbal communications
High attention to detail
Decision-making and AutonomyAble to manage projects, programs and tasks with little, to no, oversight. Able to analyze data and make recommendations to management and/or escalate as appropriate.
InteractionExperience working within complex/matrixed organizations
Demonstrated ability to collaborate with and achieve results through others, the ability to build strong and sustainable relationships and the capability to interact within all levels of the organization
InnovationAbility to read, analyze and interpret common scientific and technical data/reports and legal/regulatory documents
Effectively presents information to management, internal groups, and stakeholders
ComplexityAnalytical capabilities with the ability to analyze a wide variety of information and data to determine potential risks
Ability to anticipate potential problems and risks related to quality expectations and regulatory compliance, formulate action plans, and implement solutions
Ability to work effectively in a fast paced, rapidly changing environment and to work on multiple work streams and projects simultaneously
Important Considerations
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection.
Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
Work in a cold, wet environment.
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
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.#GMSGQ #ZR1 #LI-MA1Takeda Compensation and Benefits SummaryWe 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 StatementTakeda 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
Job ExemptYes#J-18808-Ljbffr