Supplier Quality Management Expert

☞ Takeda

看过: 110

更新日: 26-11-2025

位置: Lessines Hainaut

类别: 质量保证/质量控制

行业: Pharmaceutical Manufacturing

水平: Entry level

工作类型: Full-time

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工作内容

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Job Description

About the role

At Takeda’s Lessines plant, we blend science, dedication, and a drive for quality. We’re seeking a professional to helm our Supplier Quality and Material Management programs, an endeavor that bridges robust supplier relationships with global alignment and regulatory acumen.

Dive into a role where empathy meets precision, and your deep knowledge becomes our shared pathway to excellence.

How You Will Contribute
  • You will be driving the development, deployment, execution and maintenance of the Supplier Quality and Material Management programs at the Lessines plant.
  • Executing of global supplier and material/product management and audit activities for the suppliers assigned to the Lessines plant.
  • Support the coordination with Global Supplier Quality management group and global audit planning.
  • Performing external audits as needed (up to 15 % travel time due to audits).
  • Executing of qualification, maintenance and monitoring for the plant’s local suppliers, with an emphasis on continuous improvement, global alignment, risk management and supply chain reliability.
  • Partnering with the business and key stakeholders to drive continuous improvement in Quality performance across the plant and the company.
  • Supporting local cross-functional stakeholders and stakeholders in the Plasma Business Unit.
  • Executing the strategic direction and oversight pertaining to external auditing and supplier quality and material management.
  • Providing performance metrics to drive continuous improvement of the programs.
What You Bring To Takeda
  • Scientific degree (Bachelor or Master).
  • 3 - 5+ years of experience combined with good knowledge of the manufacturing industry (Pharma or biotech would represent a great value).
  • Experience with Quality pillars (QA, QC, Systems or Compliance, Services and Improvement).
  • Understanding of local and global regulations. Experience working with regulatory agencies and/or direct interface experience with regulatory agencies during inspections is preferred but isn’t a must.
  • Fluent in written and spoken French and a very good English.
  • Communication skills engaging stakeholders site, business, network, company, regulators.
  • Personal accountability for results and integrity.
  • Critical thinking, analytical, technical writing,
  • Ability to drive change.
  • Ability to present key quality/department/business concepts to senior representatives of external business partners and internal senior leadership teams.
  • Expertise with Word, Excel, PowerPoint and SharePoint.
  • Your eagerness to be part of a vibrant and collegial team of professionals.
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.

Empowering our people to shine

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, or characteristics, marital or other status. At Takeda, we embrace diversity as a whole.

Locations

BEL - Lessines

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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最后期限: 10-01-2026

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