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R0057670 Leader, BD & CMB Quality (Open). Zürich. Suiza

Trabajos de Tenedores de libros en Suiza (Zürich)

Clasificación del trabajo: Técnicos y profesionales de nivel medio › Profesionales de nivel medio en operaciones financieras y administrativas › Profesionales de nivel medio en finanzas y matemáticas › Tenedores de libros.

Traducción de la profesión: Techniker und gleichrangige nichttechnische Berufe › Nicht akademische betriebswirtschaftliche und kaufmännische Fachkräfte und Verwaltungsfachkräfte › Nicht akademische Fachkräfte im Bereich Finanzen und mathematische Verfahren › Nicht akademische Fachkräfte im Rechnungswesen.

Descripción de la oferta de trabajo:

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 that will 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.

About the role:


Manage assigned due diligence and divestiture activities for Quality Support Due Diligence activity through engagement with regional Quality teams to provide professional and detailed quality support to support Takeda Business Development and Divestiture projects Develops Quality strategy for management of external partnerships and management of CMB customers. Manages partnerships where product is out-licensed i.e. where ownership belongs to third party or shared with Takeda Primary Quality contact for CMB customer(s) for QIM, Inspections, Audits, QMS communication and product release support

Delegates tasks associated Business Process ownership of Business Development & Due Diligence and CMB business support.

How you will contribute:


Manage Quality Divestiture and Due Diligence activities worldwide in conjunction with the Head, BD & CMB Quality.

Support the execution of divestiture plans, collaborating with management, HR, legal, Finance and all necessary functions to ensure a smooth process and timeline

Interface regularly with BD leads for deals, and collaborate with buyer teams to execute divestiture plans in a manner consistent with Takeda’s values of PTRB

Lead quality related activities in support of divestiture implementation project teams

Execute Internalization Operating Model (IOM) inconjunction with Pharmaceutical Sciences and GMS-BD

Lead the development of an Externalization Operating Model (EOM) inconjuction with Pharmaceutical Sciences, GMS-BD, GBD and CEI.

Manage relationship between CMB Customer(s) and Takeda manufacturing plants

Support CMB related change controls and appropriate regulatory filings to ensure proper and consistent regulatory compliance

Quality lead supporting business growth in due diligence and divestment activities and works in partnership with relevant stakeholders to influence quality, supply and regulatory strategy.

Participate in or facilitate multi-site product quality investigations teams. Supports the Incident Escalation process.

Provide strategic guidance regarding the timely implementation of multi-site global changes with regulatory impact

Enact global audit policies, guidance, standards, procedures governing self inspection, risk identification and auditing

Execute duties associated with one or more of the following:

Business Process ownership of IOM and EOM processes

Business Development & Due Diligence: provide subject matter expertise to enable decision making; identifying quality related risks to projects and the provision of appropriate resolutions

Support/attend site visits/audits by CMB customer(s) with manufacturing plants

Participate in CMB customer(s) business meeting

Establish, align, and trend Quality metrics between CMB customer(s) and manufacturing plants

Project Management:  Oversee Project Management activities within the group including visibility, tracking, implementation and governance through change and project management

Track closure of divestiture TSAs

Establish business process for externalization operating model and align with partner organizations (GMS, RA, GS)

Other duties as assigned


Technical/Functional (Line) Expertise

Knowledge and experience of Bio-Pharmaceutical, R&D and/ or Vaccines Manufacturing

Knowledge and understanding of therapeutic areas as well as scientific advances and modalities for treating diseases.

Knowledge and understanding of relevant regulations enabling effective partnerships across the organization


Ability to lead cross functional teams in support of Divestiture activities and In-licensing activities

Tactical role to help develop, deploy and govern the Quality CMB processes and tools to sites / regions and global function

Decision-making and Autonomy

A member of the BD & CMB Quality team

Responsible for risk identification for internal sites and operating units and resolution of incidents


Partner with Operating units to support business priorities from a CMB, business development and divestiture perspective

Externally this role will interact with executives and implementation teams of potential buyers, CMB customers, management and strategy consultants

Partner with Operating units to support business priorities from a Quality perspective

Communicate and train sites, operating units and global functions regarding business development due diligence


A firm grasp of industry, scientific and regulatory trends, understands market conditions, and leverages innovation to evolve Takeda’s regulatory profile to become the model for the industry


The complexity in the role lies in the diversity of manufacturing techniques and facilities as the role covers all geographies and therapeutic areas

Must be able to travel domestically and internationally 30-50%

What you bring to Takeda:


Scientific degree (BSc, MSc)

15 years of increasing management responsibility combined with knowledge of pharmaceutical manufacturing

Experience across all of the Quality pillars (QA, QC, Systems and Compliance, Services and Improvement) and working in an international environment

Fluent in written and spoken English

Core Competencies / Skills

Critical Thinking

Current on local and global regulations

Digital and analytical skills

Investigation and problem solving

Strong communication skills engaging stakeholders: site, business, network, company, regulators

Risk identification, evaluation and management

Continuous improvement

Leadership Behaviors

Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust

Creating the environment that inspires and enables people

Focusing on the few priorities and provide superior results

Elevating capabilities for now and the future

País del trabajo: Suiza.

Región: Zürich.

Ver 643 ofertas de trabajo en "Zürich" (Suiza).

Número de puestos: 1.

Empleador: Takeda Pharmaceuticals International AG.

Instrucciones para solicitar:

Forma de contacto:

  • Teléfono: +35 31 429 77 56
  • Sitio web:

Oferta de trabajo obtenida del portal Eures, con fecha 12 de Abril de 2022, y con identificador de la vacante:062d2e78-8a6f-11ec-97af-baccfefb1517.

Ver las 257 ofertas de trabajo de Técnicos y profesionales de nivel medio › Profesionales de nivel medio en operaciones financieras y administrativas › Profesionales de nivel medio en finanzas y matemáticas › Tenedores de libros ofertadas.

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