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Senior Engineer Computerized System Validation
Senior Engineer Computerized System ValidationTAKEDA PHARMACEUTICALS AMERICA, INC. • Social Circle, GA, US
Senior Engineer Computerized System Validation

Senior Engineer Computerized System Validation

TAKEDA PHARMACEUTICALS AMERICA, INC. • Social Circle, GA, US
1 day ago
Job type
  • Full-time
Job description

Join to apply for the Senior Engineer Computerized System Validation role at TAKEDA PHARMACEUTICALS AMERICA, INC.

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Join to apply for the Senior Engineer Computerized System Validation role at TAKEDA PHARMACEUTICALS AMERICA, INC.

Skills

On the Global Manufacturing and Supply (GMS) team at Takeda, you'll be part of a rapidly transforming industry that's applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms :

  • Small Molecules
  • Biologics
  • Plasma
  • Cell and Gene

Skills

On the Global Manufacturing and Supply (GMS) team at Takeda, you'll be part of a rapidly transforming industry that's applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms :

  • Small Molecules
  • Biologics
  • Plasma
  • Cell and Gene
  • As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.

    Back to nav

    Job ID R0153071 Date posted 06 / 24 / 2025 Location Social Circle, Georgia

    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'sPrivacy Noticeand 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 Computerized Systems Validation Engineering, is responsible for leading, managing, and performing engineering operations within the organization. This role ensures that standards of quality, cost, safety, reliability, timeliness, and performance are met in production processes. By applying advanced knowledge and working independently with limited supervision, this role contributes to the successful completion of engineering projects.

    Responsibilities

    You will support site projects, technical transfers, and ongoing validation maintenance. Responsible for the design, authorship, and execution of commissioning, qualification and validation studies for the any or more of the following major disciplines :

  • Facilities, Utilities, and Equipment (FUE) qualification
  • Units operations automation qualification with Honeywell, Delta V, and PCL-based systems
  • Computerized systems validation
  • Cleaning validation
  • Sterilization validation
  • Materials validation
  • Process validation
  • Provides technical subject matter expert (SME) support to change controls, investigations, deviations, and CAPAs. Individual must work on moderate to complex assignments, where analysis of situations or data requires an in-depth evaluation of factors or intangible variables

    How You Will Contribute

  • Design, executes, and summarizes commissioning, qualification, and validation studies, collaborating with SMEs to ensure efficient testing strategies.
  • Conduct risk and impact assessments, develops, and reviews SOPs, validation assessments, and interfaces with customers on technical issues.
  • Participate in audits, inspections, and cross-functional investigations to identify root causes and corrective actions.
  • Calculates, interprets data, and supports best practices for validation per industry guidelines.
  • Lead small, complex projects with program managers and operations teams.
  • Demonstrate continuous improvement in validation expertise within biopharmaceuticals.
  • What You Bring To Takeda

  • Bachelor's degree in engineering with minimum 7 years validation experience.
  • 7 years of relevant experience in a GMP regulated environment.
  • At least 4 years of commissioning, qualification and validation (CQV).
  • Technical experience of automation platforms, such as DeltaV, Honeywell, Rockwell PLC, Siemens XFP7.
  • Knowledge working with Building Automation Systems (BAS) Honeywell
  • Knowledge working with Data Historian Systems (DHS) like OSI PI
  • Basic knowledge of networks, interfaces, and OPC
  • Building practical experience with Systems Engineering, applies basic principles with guidance.
  • Building practical experience with algorithms, begins to apply them in simple situations with support.
  • Have a basic understanding of systems modeling, apply it with guidance in simple projects.
  • Lead validation projects, coordinate contractors, and drive results.
  • Direct experience manufacturing operations and biotechnology processes is desired.
  • 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 around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
  • May be required to work weekends, evenings, off-hours, extended periods of time.
  • Occasionally, may be required to lift up to 50 pounds, and be able to walk, stand, reach and stoop.
  • Up to 10% travel expected.
  • 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.

    GMSGQ

    ZR1

    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 - GA - Social Circle - Hwy 278

    U.S. Base Salary Range

    $86,500.00 - $135,960.00

    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 - GA - Social Circle - Hwy 278

    Worker Type

    Employee

    Worker Sub-Type

    Regular

    Time Type

    Full time

    Job Exempt

    Yes

    Apply Now

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    Seniority level

    Seniority level

    Mid-Senior level

    Employment type

    Employment type

    Full-time

    Job function

    Job function

    Quality Assurance

    Industries

    Pharmaceutical Manufacturing

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