Associate Director, Quality Control
Location: Libertyville
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 The
Associate Director of Quality Control will lead the establishment
of a state-of-the-art quality control laboratory. Responsibilities
include overseeing its design, construction, qualification, and
regulatory approval. Collaborate with global teams to align with
Takeda’s laboratory-of-the-future strategy, focusing on automation
and paperless systems. Hire and train the Quality Control team,
eventually overseeing lab operations to support a 24/7
pharmaceutical manufacturing site. How you will contribute ·Lead
the planning and execution of a new Quality Control Laboratory
startup, ensuring full compliance with regulatory standards.
·Design and implement efficient lab processes and workflows to
optimize operational performance and throughput. ·Collaborate
cross-functionally with IT, R&D, and Manufacturing to ensure
seamless system integration. ·Oversee the selection, validation,
and implementation of laboratory automation technologies and LIMS
platforms. ·Develop and enforce SOPs that uphold the highest
standards of safety and quality. ·Manage resources, timelines, and
deliverables to ensure a successful and timely lab launch.
·Recruit, train, and lead a high-performing laboratory team,
fostering a culture of excellence and accountability. ·Stay current
with industry best practices, emerging technologies, and regulatory
developments to drive innovation. ·Develop and manage departmental
budgets, ensuring alignment with organizational goals and fiscal
responsibility. ·Promote team development, engagement, and
retention through effective leadership and mentorship. ·Communicate
and present effectively to senior leadership and key stakeholders.
·Supervise and support technical teams in a regulated environment,
ensuring operational excellence. ·Lead and support regulatory
audits and submissions with confidence and precision. ·Maintain
clear and consistent communication with the Site Quality Head
regarding quality and safety matters. What you bring to Takeda
·Bachelor’s degree in science, engineering, or a related technical
field. ·Minimum of 8 years of industry experience, including at
least 3 years in a managerial or leadership role. ·Demonstrated
expertise in Quality Assurance, Quality Control, and laboratory
startup operations. ·Strong working knowledge of FDA regulations,
current Good Manufacturing Practices (cGMP), and EU regulatory
standards. ·Proven ability to lead teams and thrive in dynamic,
fast-paced environments. ·Proficient in assessing quality risks and
authorized to approve or reject laboratory results. ·Active
participation in global forums to stay informed on industry
innovations and best practices. ·Deep understanding of Quality
Control and Sterility Assurance, including experience with
technical upgrades and system improvements. ·Skilled in applying
risk management principles to daily operations and decision-making.
·Ability to safely manage hazardous and biological materials in
compliance with safety protocols. About our Round Lake Facility:
Takeda's manufacturing facility in Round Lake, Illinois, is an
integral part of Takeda’s Plasma Network. Close in proximity to
both Chicago and Milwaukee, the state-of-the-art facility
specializes in producing Flexbumin through the GALAXY manufacturing
process. Flexbumin is albumin, contained in a flexible pouch, for
patients who experience a loss of plasma volume from situations
such as trauma, surgery, blood loss and burns. Round Lake supplies
its product to patients all over the world, with key markets in the
U.S., China, and India. Join us to make a difference. What Takeda
can offer you: Comprehensive Healthcare: Medical, Dental, and
Vision Financial Planning & Stability: 401(k) with company match
and Annual Retirement Contribution Plan 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 and company match of charitable
contributions Family Planning Support Flexible Work Paths Tuition
reimbursement 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: Work
in a controlled environment requiring special gowning and wear
protective clothing over the head, face, hands, feet and body. This
may include additional hearing protection for loud areas. 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. This posting excludes
Colorado applicants. Empowering our people to shine: 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. GMSGQ
LI-FM1 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 - IL - Round Lake Innovation Park 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 - IL - Round Lake
Innovation Park Worker Type Employee Worker Sub-Type Regular Time
Type Full time Job Exempt Yes
Keywords: , Rockford , Associate Director, Quality Control, Science, Research & Development , Libertyville, Illinois