Bio Process Sciences Lead (Sr. Manager)
Takeda Pharmaceutical —Zürich, ZH
- CHF 159’300 - CHF 219’010 pro Jahr
- Überstunden
- Management-Erfahrung
- Doktorat
- Englisch
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Bio Process Sciences Lead (Sr. Manager)

Takeda Pharmaceutical -
Zürich, ZH

Jetzt bewerben

Details zur Stelle

100%
CHF 159’300 - CHF 219’010 pro Jahr

Qualifikationen

Management-Erfahrung
Doktorat
Englisch
Master
Bachelor
Produktion
Führungserfahrung
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

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

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 Takeda’s 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 Takeda’s global network. This is a high‑visibility 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:

Bachelor’s 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

CHE - Glattpark (Opfikon) - Zurich HQUSA - MA - Lexington

Base Salary Range:

CHF159,300.00 - CHF219,010.00

For information about our benefits, please click here.

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Jetzt bewerben

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