Associate Director Quality Assurance
Location: Thousand Oaks
Posted on: June 23, 2025
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Job Description:
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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: As the
Head of Quality Assurance you will lead quality oversight to ensure
that all products meet applicable regulatory and Takeda quality
standards across global markets. You will oversee critical quality
systems including batch record review, product release, change
control, deviation management, and annual product reviews, while
driving compliance with cGMP and regulatory requirements. You will
contribute in global and site-level strategic initiatives, supports
regulatory inspections, and provides direction during
quality-impacting incidents. Additionally, this position is
accountable for resource and budget management, talent development,
and succession planning to support long-term organizational
success. You will report into the Site Quality Head. How you will
contribute: Assure adequate Quality oversight that meets product
requirements to applicable geographies Ensure adherence to facility
quality systems such as batch record review, product release,
change control, deviation management, and product annual reviews
Manage resources, to ensure production and product release cycle
times are met for supply chain demands Participate on Global Core
teams, site strategic projects Identify and assess quality risks in
activities and ensure conformance to Takeda quality policies, and
government regulations Support Quality Assurance Programs to
improve safety, customer satisfaction, employee development,
continuous improvement, and financial performance consistent with
Site goals Lead the product disposition at the site for all
product, including deviation quality review and disposition of
product Provide support for several activities to ensure compliance
with quality objectives and regulatory requirements Manage
resources to ensure production and release cycle times are met for
supply chain demands Support new product introductions to the site
Technical skills and substantial knowledge of industry best
practices and trends Set annual budget and manage resources to meet
annual budget Implement lean concepts to improve cycle times within
the area Work with manufacturing management in cGMP compliance and
quality systems Provide direction in the event of manufacturing
incidents that may potentially affect quality or compliance
Responsible for management of investigations, CAPAs, batch record
review, assisting with product release, change control,
requalification, and product annual review in the manufacturing
area Work with manufacturing teams in proactive functions that
impact production, solve problems, improve quality, increase
efficiency, generate cost savings, and provide new product support
Responsible for approval of changes within the manufacturing area
including changes to process, equipment, procedures, and
computerized systems Ensure compliance with current regulatory or
product license requirements and cGMPs Support the Thousand Oaks
facility during external and regulatory inspections Work directly
with the investigators on defending facility quality systems and
product investigations Hire and retain great talent; develop and
provide challenging work for team members; support the career
development of their employees both within their current position
as well in situations where employees move on to different roles
within the Takeda organization; manage performance and
differentiate compensation and development; plan for future talent
needs; improve performance Minimum Requirements/Qualifications:
Bachelor's degree in related field Minimum 10 years' experience in
a manufacturing or quality operations function in a biotechnology,
biologics, or pharmaceutical manufacturing facility Minimum 5 years
previous leadership, supervisory or management experience required
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. 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: USA - CA - Thousand Oaks - Rancho Conejo
U.S. Base Salary Range: $153,600.00 - $241,340.00 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-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 USA - CA - Thousand Oaks
- Rancho Conejo Worker Type Employee Worker Sub-Type Regular Time
Type Full time Job Exempt Yes
Keywords: , Los Angeles , Associate Director Quality Assurance, Science, Research & Development , Thousand Oaks, California