Job Detail

Process Scientist Manager

Inseriert am: 23.06.2021

Process Scientist Manager


Lexington, Massachusetts, Zurich, Switzerland

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  • Overview

  • Success

  • Life at Takeda

  • Opportunity

  • Responsibilities

  • Map


Overview


Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.


Global Manufacturing and Supply Chain, and Global Quality is the backbone of Takeda, and our employees are the guardians for our patients, our products, and our reputation. As a member of our team, we can offer you the opportunity to grow in a meaningful career, develop your skills, and come to work every day knowing that what you do makes a genuine difference.


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Success


What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.



  • Agile

  • Ambitious

  • Analytical

  • Collaborative

  • Enthusiastic

  • Entrepreneurial


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Life at Takeda



  • A Global Top Employer

    Recognized for our culture and way of working, we’re one of only select companies to receive Top Global Employer® status for 2021.


  • At Takeda, your determination and energy, combined with our cutting-edge technology and global R&D, offers families and communities hope for Better Health and a Brighter Future.

    Global Manufacturing

    Learn more about Manufacturing, Supply Chain, and Quality careers within our global biopharmaceutical company.


  • About Takeda

    At Takeda, there is an unwavering commitment to putting patients first, and to creating a workplace that is underpinned by empowerment and focused on diversity, collaboration and steadfast values.



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Opportunity



  • Innovation

    Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.


  • Inclusive

    Here, you will feel welcomed, respected, and valued as a vital contributor our global team.


  • Empowerment

    Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.


  • Collaboration

    A strong, borderless team, we strive together towards our priorities and inspiring mission.


  • Top Workplace

    Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2021.


  • Work-Life

    Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.



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Process Scientist Manager

Apply NowJob ID R0027310Date posted 04.20.2021Location Lexington, Massachusetts; Zurich, Switzerland

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


OBJECTIVES/PURPOSE



  • Member of the global team of process science experts responsible for the manufacturing process for Takeda’s large and diverse commercial biologics portfolio

  • Acts as a senior subject matter expert across the biologics portfolio

  • Provides technical expertise and leadership for regulatory interactions, including authoring CMC content for multi-site products

  • Independent Contributor Manager: overseeing projects and function


ACCOUNTABILITIES



  • Provide upstream and downstream technical expertise and leadership for various projects across the biologics portfolio, including: lifecycle initiatives to enable supply continuity, risk management, line extensions & discontinuation, process tech transfers, global expansion/contraction, regulatory activities, and capability & improvement.

  • Ensure technical continuity of manufacturing processes across sites and time

  • Provide technical expertise for initiatives and investigations which are complex or span across multiple products

  • Lead process improvement projects that span sites or products

  • Ensure alignment of CMC content for multi-site products

  • Provide technical expertise required to maintain control strategy documents


DIMENSIONS AND ASPECTS


Technical/Functional (Line) Expertise



  • Has a good understanding of biologics manufacturing, the regulatory environment, life cycle management, and trends in innovation


Leadership



  • Ability to influence within teams to drive decisions, alignment, and conflict resolution for complex cross-functional issues

  • Being a mentor developing future leaders

  • Displays and drives Takeda culture of Takeda-ism, PTRB, safety, and quality into the organization


Decision-making and Autonomy



  • Represents Bio Process Sciences on various teams and is empowered to work within the team to align on decisions


Interaction



  • Provides feedback within Bio Process Sciences to ensure LCM alignment across products

  • Works with site MS teams on process improvement projects and other LCM projects

  • Works within product governance teams to align on effective product LCM

  • Works with Biologics Process Development on process improvements and other LCM projects


Innovation



  • Provides technical input to Biologics Process Development for process improvement and other LCM projects

  • Ensures process knowledge sharing across sites to ensure technical continuity for multi-site products


Complexity



  • Provides leadership on cross-functional teams

  • Provides leadership to drive highly complex projects including ones that span multiple sites and products


EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:


Education / experience



  • BS in engineering, life sciences, or related field with a Minimum 10 years experience, MS with a minimum of 8 years experience, or PhD with 0-5 years experience in pharmaceutical development and manufacturing

  • Experience operating globally in a matrixed organization highly preferred


Skills



  • Must have technical knowledge and experience in upstream or downstream process development

  • Must be self-motivated, have good interpersonal skills, capable of analyzing and solving complex problems through innovative thought and experience.


Behaviors



  • Focusing on the few priorities and provide superior results

  • Elevating capabilities for now and the future

  • Provide leadership on cross-functional teams


This job posting excludes CO applicants.


Locations

Lexington, MAZurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time



Job ID R0027310Apply NowEmail Me

Back to Job Navigation (Responsibilities)


Process Scientist Manager

Apply NowJob ID R0027310Date posted 04.20.2021Location Lexington, Massachusetts; Zurich, Switzerland

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


OBJECTIVES/PURPOSE



  • Member of the global team of process science experts responsible for the manufacturing process for Takeda’s large and diverse commercial biologics portfolio

  • Acts as a senior subject matter expert across the biologics portfolio

  • Provides technical expertise and leadership for regulatory interactions, including authoring CMC content for multi-site products

  • Independent Contributor Manager: overseeing projects and function


ACCOUNTABILITIES



  • Provide upstream and downstream technical expertise and leadership for various projects across the biologics portfolio, including: lifecycle initiatives to enable supply continuity, risk management, line extensions & discontinuation, process tech transfers, global expansion/contraction, regulatory activities, and capability & improvement.

  • Ensure technical continuity of manufacturing processes across sites and time

  • Provide technical expertise for initiatives and investigations which are complex or span across multiple products

  • Lead process improvement projects that span sites or products

  • Ensure alignment of CMC content for multi-site products

  • Provide technical expertise required to maintain control strategy documents


DIMENSIONS AND ASPECTS


Technical/Functional (Line) Expertise



  • Has a good understanding of biologics manufacturing, the regulatory environment, life cycle management, and trends in innovation


Leadership



  • Ability to influence within teams to drive decisions, alignment, and conflict resolution for complex cross-functional issues

  • Being a mentor developing future leaders

  • Displays and drives Takeda culture of Takeda-ism, PTRB, safety, and quality into the organization


Decision-making and Autonomy



  • Represents Bio Process Sciences on various teams and is empowered to work within the team to align on decisions


Interaction



  • Provides feedback within Bio Process Sciences to ensure LCM alignment across products

  • Works with site MS teams on process improvement projects and other LCM projects

  • Works within product governance teams to align on effective product LCM

  • Works with Biologics Process Development on process improvements and other LCM projects


Innovation



  • Provides technical input to Biologics Process Development for process improvement and other LCM projects

  • Ensures process knowledge sharing across sites to ensure technical continuity for multi-site products


Complexity



  • Provides leadership on cross-functional teams

  • Provides leadership to drive highly complex projects including ones that span multiple sites and products


EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:


Education / experience



  • BS in engineering, life sciences, or related field with a Minimum 10 years experience, MS with a minimum of 8 years experience, or PhD with 0-5 years experience in pharmaceutical development and manufacturing

  • Experience operating globally in a matrixed organization highly preferred


Skills



  • Must have technical knowledge and experience in upstream or downstream process development

  • Must be self-motivated, have good interpersonal skills, capable of analyzing and solving complex problems through innovative thought and experience.


Behaviors



  • Focusing on the few priorities and provide superior results

  • Elevating capabilities for now and the future

  • Provide leadership on cross-functional teams


This job posting excludes CO applicants.


Locations

Lexington, MAZurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time



Job ID R0027310Apply NowEmail Me

Details