Santa Rufina, Italy, Rieti, Italy
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.
What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.
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 2019.
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.
Learn more about Manufacturing, Supply Chain, and Quality careers within our global biopharmaceutical company.
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.
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.
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.
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