Job Detail

Manufacturing Associate - Fixed-term contract 7 months

Inseriert am: 23.02.2021

Manufacturing Associate - Fixed-term contract 7 months


Neuchâtel, Switzerland

Apply NowEmail Me

  • 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.


Back to Job Navigation (Overview)


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


Back to Job Navigation (Success)


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.



Back to Job Navigation (Life at Takeda)


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.



Back to Job Navigation (Rewards)


Manufacturing Associate - Fixed-term contract 7 months

Apply NowJob ID R0025978Date posted 12.16.2020Location Neuchâtel, Switzerland

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.


Job Description


Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine.


Here, everyone matters, and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.


An exciting and challenging opportunity has become available at Takeda’s Neuchatel Manufacturing plant (approx. 650 employees) for an experienced


Manufacturing Associate - Fixed-term contract 7 months


to join our Manufacturing support team.


This is an exciting career opportunity for a dynamic, autonomous, continuous improvement minded and change agile manufacturing professional to embrace a team-based culture and more specifically within the manufacturing teams within a world-class Biotech manufacturing environment.


Your mission


Within the Manufacturing Department, reporting to the Manufacturing Support Group, the purpose of this role is primarily to provide the technical expertise needed to investigate deviations within the manufacturing process and to act as a catalyst for continuous improvement. Main responsibilities of the Manufacturing Support Group are problem solving, creation of added value, standardization and improvement of manufacturing processes


Essential Duties & Responsibilities


As a deviation owner for the Manufacturing Department:



  • Initiate and manage deviations within the framework of production events and within quality systems (i.e. Trackwise) in a timely manner

  • Perform evaluations related to impact on concerned equipment/product/material with the support of relevant Subject Matter Experts (SME)

  • Perform investigations of moderate complexity/severity using root cause analysis tools (e.g. DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.), including management of investigation team as appropriate

  • Determine corrective and preventive actions (CAPA)

  • Write complete investigation report and impact assessment

  • Participate and support Manufacturing Engineers for investigations of high criticality events

  • Support internal and external audits preparation as a Subject Matter Expert (SME) for selected topics

  • Participate to manufacturing process improvement and/or enhancement projects

  • Incorporates and respects cGMP concepts (Good Manufacturing Practices)


Required Skills



  • Strong knowledge and interest in detailed manufacturing operations (e.g. engineering designs, automated documentation) and biotechnological processes (USP and/or DSP).

  • Ability to think and act cross-functionally, interacting with various SME (EHS, QA, QC, engineering, projects, etc.).

  • Structured, rigorous and self-motivated

  • Able to work in a fast and dynamic environment with a high emphasis on achieving results

  • Demonstrate excellent communication skills orally and written, ability to describe complex technical processes and qualifications and to translate it into clear, precise reports

  • Team player prepared to work in a team-based culture including with the manufacturing personnel on the production floor, ability to listen and adapt to the audience.

  • Fluency in French, good oral and written skills in English


Education & Experience



  • CFC, HES Diploma or Bachelor in Biotechnology or Pharmaceutical Engineering and 3-5 years of experience within a biotech/pharmaceutical manufacturing environment

  • Technical knowledge of the biotechnological processes (USP and/or DSP)

  • Ideally demonstrated experience in “deviation” management including use of Six Sigma tools (e.g. DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.)

  • Experience of Quality/Compliance requirements within aGMP manufacturing environment


Working Environment



  • While this is a day-time job, must be able to work on occasions in controlled environments (ISO 5, ISO 7 and ISO 8 environments; grade A, B and C) requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.


Locations

CHE - Neuchatel

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time



Job ID R0025978Apply NowEmail Me

Back to Job Navigation (Responsibilities)


Manufacturing Associate - Fixed-term contract 7 months

Apply NowJob ID R0025978Date posted 12.16.2020Location Neuchâtel, Switzerland

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.


Job Description


Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine.


Here, everyone matters, and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.


An exciting and challenging opportunity has become available at Takeda’s Neuchatel Manufacturing plant (approx. 650 employees) for an experienced


Manufacturing Associate - Fixed-term contract 7 months


to join our Manufacturing support team.


This is an exciting career opportunity for a dynamic, autonomous, continuous improvement minded and change agile manufacturing professional to embrace a team-based culture and more specifically within the manufacturing teams within a world-class Biotech manufacturing environment.


Your mission


Within the Manufacturing Department, reporting to the Manufacturing Support Group, the purpose of this role is primarily to provide the technical expertise needed to investigate deviations within the manufacturing process and to act as a catalyst for continuous improvement. Main responsibilities of the Manufacturing Support Group are problem solving, creation of added value, standardization and improvement of manufacturing processes


Essential Duties & Responsibilities


As a deviation owner for the Manufacturing Department:



  • Initiate and manage deviations within the framework of production events and within quality systems (i.e. Trackwise) in a timely manner

  • Perform evaluations related to impact on concerned equipment/product/material with the support of relevant Subject Matter Experts (SME)

  • Perform investigations of moderate complexity/severity using root cause analysis tools (e.g. DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.), including management of investigation team as appropriate

  • Determine corrective and preventive actions (CAPA)

  • Write complete investigation report and impact assessment

  • Participate and support Manufacturing Engineers for investigations of high criticality events

  • Support internal and external audits preparation as a Subject Matter Expert (SME) for selected topics

  • Participate to manufacturing process improvement and/or enhancement projects

  • Incorporates and respects cGMP concepts (Good Manufacturing Practices)


Required Skills



  • Strong knowledge and interest in detailed manufacturing operations (e.g. engineering designs, automated documentation) and biotechnological processes (USP and/or DSP).

  • Ability to think and act cross-functionally, interacting with various SME (EHS, QA, QC, engineering, projects, etc.).

  • Structured, rigorous and self-motivated

  • Able to work in a fast and dynamic environment with a high emphasis on achieving results

  • Demonstrate excellent communication skills orally and written, ability to describe complex technical processes and qualifications and to translate it into clear, precise reports

  • Team player prepared to work in a team-based culture including with the manufacturing personnel on the production floor, ability to listen and adapt to the audience.

  • Fluency in French, good oral and written skills in English


Education & Experience



  • CFC, HES Diploma or Bachelor in Biotechnology or Pharmaceutical Engineering and 3-5 years of experience within a biotech/pharmaceutical manufacturing environment

  • Technical knowledge of the biotechnological processes (USP and/or DSP)

  • Ideally demonstrated experience in “deviation” management including use of Six Sigma tools (e.g. DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.)

  • Experience of Quality/Compliance requirements within aGMP manufacturing environment


Working Environment



  • While this is a day-time job, must be able to work on occasions in controlled environments (ISO 5, ISO 7 and ISO 8 environments; grade A, B and C) requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.


Locations

CHE - Neuchatel

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time



Job ID R0025978Apply NowEmail Me