Quality Validation Engineer II
Location: Libertyville
Posted on: June 23, 2025
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Job Description:
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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 The Quality Validation
Engineer II ensures the quality of processes and product outputs.
You will define activities, processes, and standards to meet
quality requirements, auditing and monitoring processes, and
reporting on deviations and defects. By maintaining high standards,
you will support Takeda's mission to deliver quality products. You
will report to the Quality Validation Manager. About the role: The
Quality Validation Engineer II position is in the Validation
Quality organization at the Takeda Round Lake aseptic
pharmaceutical manufacturing facility. You will work as part of
cross-functional teams providing quality oversight and approval of
change control and validation deliverables to ensure that products
and processes meet with appropriate regulatory agency validation
requirements, internal company standards and current industry
practices. You will typically focus on disciplines related to
equipment, cleaning, process, control system and computer system
validation. How you will contribute: Experience applying cGMPs.
Knowledge of validation principles across multiple disciplines.
Will work as a collaborative team member and, in some cases, lead a
small team to resolve small to medium scope validation issues. Must
demonstrate excellent problem-solving and understanding of complex
manufacturing processes. Experience presenting to inspection
auditors. Microsoft Office (Word, Excel, PowerPoint) skills.
Knowledge of descriptive statistics. Working knowledge of
inferential statistics and related techniques (e.g., sample size
determination, comparative analysis, ANOVA, DoE). Complete assigned
training. Identify, escalate, and resolve potential compliance and
safety issues. What you bring to Takeda: Requires a BA or BS in the
Sciences/Engineering/Chemistry or other job-related discipline. 2
years of related experience in validation within a pharmaceutical,
biotech, or related industry. Manage Standard Operating Procedures
and other Quality System Documentation relevant to their area of
expertise, and will approve Standard Operating Procedures and other
Quality System Documentation important to all plant areas. Develop
and deliver training materials relevant to their area of expertise
and will approve training materials important to all areas of the
plant. Participate as a team member in the execution and
documentation of Validation Master Plans, Design Qualification,
Installation Qualification, Operational Qualification, Performance
Qualification, Computer System Validation, and Validation
Maintenance packages, Computerized System Change Orders, Controlled
System Work Requests. Approve deliverables for compliance to
defined requirements. Experience in qualifying analytical
laboratory equipment and performing method validation Lead
cross-functional teams in the execution of risk management
activities. Approve change controls for compliance to defined
requirements. Lead Quality project teams and present to Plant
management project plans, progress, and risks. Will represent us in
areas of expertise to governmental Regulatory bodies. Important
Considerations Must be able to lift, push, pull 25 lbs and carry up
to 50 lbs. In general, your work will be a combination of sedentary
work and walking around observing conditions in the facility. Can
work in controlled environments requiring special gowning. Will
follow gowning requirements and wear protective clothing over the
head, face, hands, feet and body. No make-up, jewelry, contact
lenses, nail polish or artificial fingernails may be worn in the
manufacturing environment. Will work in a loud area that requires
hearing protection and other protective equipment to be worn. 20/20
near vision required (corrected vision is acceptable). Will work in
a cold, wet environment. Will work around chemicals such as
alcohol, acids, and alkalines that require protective equipment.
May work in a confined area. Inside and Outdoor working conditions.
Some Clean Room and cool/hot storage conditions. Perform removal of
hazardous waste. More about us: At Takeda, we are transforming
patient care through the development of novel specialty
pharmaceuticals and the best patient support programs. Takeda is a
patient-focused company to 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 - IL - Round
Lake Innovation Park U.S. Base Salary Range: $70,000.00 -
$110,000.00 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: , Glenview , Quality Validation Engineer II, Science, Research & Development , Libertyville, Illinois