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Sr Development Engineer I

Company: Takeda Pharmaceutical
Location: Methuen
Posted on: August 7, 2022

Job Description:

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: Sr Development Engineer I Location: Lexington, MA About the Role: As an important member of the Technical Services - Commercial Manufacturing Support Laboratory group, you will provide technical and scientific support to upstream processes for commercial production and late-stage clinical production of biologics, through process and product investigations/troubleshooting, process improvement and life-cycle management, technology transfer and process validation. You will lead or contribute as an important member of multiple teams and will work with other departments within Takeda, including Manufacturing, PTS, QA, QC, PD, Engineering and RA . The responsibilities will include:Lead and complete process improvements, aimed at improving robustness, capacity, and productivity.Implement and sustainable process control strategy including new Process and Analytical Technologies (PAT)How you will contribute:

  • Deliver process improvements, aimed at improving robustness, capacity, and productivity.
  • Provide technical expertise and leadership in identifying opportunities/areas, planning, designing, and conducting experiments, analyzing data and documenting results towards upstream process improvement, including reducing recurring deviations and increasing level of safety and compliance.
  • Support regulatory inspections and filings as an author and reviewer
  • Implement and sustainable process control strategy including new Process and Analytical Technologies (PAT)What you bring to Takeda:
    • A PhD in Chemical Engineering or related disciplines with 1 or more years of relevant experience in a biotechnology/pharmaceutical environment; or MS in Chemical Engineering or related disciplines with 5 years of experience; or BS in Chemical Engineering or related disciplines with 8 years of experience is required.
      • Hands-on experience in process characterization leading to definition of design space.
      • Experience in implementation of process control strategy using QbD principles.
      • Experience in implementation of disposables in manufacturing of biologics.
      • Have experience with mammalian cell culture process development, scale-up and scale-down, tech transfer and GMP manufacturing support.
      • Have experience in design-of-experiment (DoE) and the ability to analyze and interpret data collected.
      • Demonstrate teamwork.
      • Be customer focused, science driven and embrace values.
      • learn new technologies and manage changes in upstream process development and improvement.
      • Have experience in GMP working environments.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
        • Professional development opportunities
        • Tuition reimbursementAt 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. 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..
          • Work multiple shifts, including weekends, or be asked to work supplemental hours.
          • 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 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.This posting excludes Colorado applicants.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 - MA - Lexington - BIO OPS Worker Type Employee Worker Sub-Type Regular Time Type Full time

Keywords: Takeda Pharmaceutical, Methuen , Sr Development Engineer I, Engineering , Methuen, Massachusetts

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