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Business&Compl.Excell.Manager

Santa Rufina, Italy, Rieti, Italy

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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Opportunity

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

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

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

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

  • Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2018.

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

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Business&Compl.Excell.Manager

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Job ID SR0043826 Date posted 11/04/2019 Location Santa Rufina, Italy; Rieti, Italy

The candidate coordinates strategy, system, and cultural integration towards Compliance Excellence for the facility. Assures alignment

with Division and Corporate Compliance Excellence initiatives. Coordinates multiple complex and cross-functional Facility

project to drive continuous improvement in GMP Compliance. Develops metrics and presentations for the purposes of

communicating project status to Senior Management.

Assures the definition of a local Compliance Excellence program, use PMM and QLP methodology:

Helps identify and communicate resource needs and support the commitment process

Develops a Compliance Excellence project plan and promotes execution to timelines and committed resources.

Communicates project status

Identifies challenges, recommends solutions and drives action plans

Leads the development of Compliance Excellence awareness, understanding, and support for these programs

Serves as the primary point of contact for the facility with respect to Compliance Excellence and represents the Facility in

all Division Compliance Excellence operating mechanisms

Coordinate the development of plant Strategic Plan and guarantee the alignment with the company/division objectives

Define the plant strategy for the execution of QLP activities: DDFP, Kaizen, DMAIC, VIPs

Guarantee the interface with divisional OLP team and present plant performance results to stakeholders

Put in place the adequate local operative mechanisms to periodically evaluate performance indicators

Coordinate/deploy a LP training programs (yellow belt, green belt, black belt, DDFP...)

Facilitate QLP/DMAIC project identification, scope, prioritization, tracking and reporting

Define VIP projects identifications, scoping, financial approval, tracking and reporting.

Required skills

Project management experience and PMM certification preferred

Lean/Six Sigma Green Belt Certification Is highly desirable

Must possess expertise In PowerPoint and creating PowerPoint Presentations.

Ability to drive change and motivate other toward a common vision

Demonstrated leadership attributes

Ability to lead teams that are not direct reports

Excellent facilitation, problem solving, and analytical skills

Experience/participation In regulatory inspections

Understanding of cGMP regulations (Us, EU, Japan, Canada, etc.) and quality management system for pharmaceutical,

device biologics or biotechnology operations as applicable to the facility.

Experience in manufacturing ancillary quality operations.

Strong knowledge of quality systems.

Excellent interpersonal/influencing/negotiating skills

Excellent communication and presentation skills, both oral and written with a demonstrated ability to present key quality/department/business indicators to senior management

Excellent project management, organizational, planning and analytical skills

Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda’s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.



Job ID SR0043826

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