Global Manufacturing Sciences BioProcess Lead (Sr. Manager)

Takeda

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profile Job Location:

Zürich - Switzerland

profile Monthly Salary: Not Disclosed
Posted on: 15 hours ago
Vacancies: 1 Vacancy

Job Summary

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 Takedas 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

Title: Global Manufacturing Sciences BioProcess Lead (Sr. Manager)

Location: Zurich Switzerland / Lexington MA

About the role:

As a Global Manufacturing Sciences Bioprocess Lead you will be an expert responsible for the manufacturing process for Takedas large and diverse commercial biologics portfolio. You will act as a senior subject matter expert across the biologics portfolio and provide technical expertise and leadership for regulatory interactions including authoring CMC content for multi-site products. You will ensure that complex multi-site biologics drug substance processes are robust well-controlled and aligned across Takedas global network. This is a highvisibility role at the interface of development manufacturing and regulatory where your decisions directly shape how innovative biologics are reliably supplied to patients worldwide.

How will you contribute:

  • Provide upstream and downstream technical expertise and leadership across the biologics portfolio including lifecycle initiatives to enable supply continuity risk management line extensions/discontinuations tech transfers global expansions/contractions and regulatory activities.

  • Ensure technical continuity of biologics drug substance manufacturing processes over time and across multiple manufacturing sites.

  • Serve as a subject matter expert in commercial biologics drug substance processes including mammalian cell culture and antibody production.

  • Lead complex technical investigations and multi-site process improvement projects that span products sites and functions.

  • Partner with site Manufacturing Sciences (MS) teams on process improvement and Life Cycle Management (LCM) projects.

  • Collaborate with Biologics Process Development on process improvements and other LCM projects providing technical input to translate development knowledge into commercial robustness.

  • Shape and align CMC content for multi-site products including authoring and reviewing regulatory filings and maintaining control strategy documents.

  • Drive process knowledge sharing across sites to support consistent execution strong control strategies and effective LCM.

  • Apply industry trends and innovation in bioprocessing to propose and implement practical process improvements and LCM initiatives.

  • Represent Bio Process Sciences on cross-functional and product governance teams influencing decisions and aligning on effective product lifecycle strategies.

What you bring to Takeda:

  • Bachelors degree in Engineering Life Sciences or a related field with 10 years of experience in pharmaceutical/biopharmaceutical development and/or manufacturing; an advanced degree (MS or PhD) is preferred.

  • Technical experience in mammalian upstream and/or downstream drug substance process development ideally with exposure to commercial-scale biologics manufacturing.

  • Experience working in a global matrixed organization collaborating with multiple sites and cross-functional teams.

  • Proven ability to analyze complex technical problems interpret process and manufacturing data and drive data-based decisions and solutions.

  • Experience contributing to regulatory filings for biologics (e.g. CMC sections control strategy documentation or responses to health authority questions).

  • Ability to lead cross-functional technical projects and to mentor or coach technical SMEs even without direct line management responsibility.

  • Strong interpersonal and communication skills with the ability to influence and align diverse stakeholders in a cross-functional setting.

  • Fluent in English (written and spoken); proficiency in Mandarin is an advantage but not required.

Locations

Zurich SwitzerlandUSA - MA - Lexington

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Required Experience:

Manager

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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...
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Key Skills

  • Lean Manufacturing
  • Six Sigma
  • Continuous Improvement
  • ISO 9001
  • Lean Six Sigma
  • Management Experience
  • Manufacturing & Controls
  • 5S
  • Manufacturing Management
  • Kaizen
  • Chemistry
  • Manufacturing

About Company

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Takeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.

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