Senior Specialist QA Packaging

☞ Takeda

Vue: 145

Jour de mise à jour: 26-11-2025

Localisation: Lessines Hainaut

Catégorie: Assurance Qualité / Contrôle Qualité

Industrie: Pharmaceutical Manufacturing

Niveau: Entry level

Type d’emploi: Full-time

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le contenu du travail

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Job Description

About the role

The purpose of this job is to act as quality expert for quality/compliance related topics in relation with the Packaging, Visual inspection and Labelling operations.

The function will also support CI and digital initiatives through the Packaging, Visual inspection and Labelling department.

How You Will Contribute

Quality Operation within his area of responsibility (Packaging and Labelling)
  • Assure the correct deployment of the cGMP, Takeda guidance within the quality operations department
  • Represent quality in significant quality-related issues, provide support and expertise. Understanding technical/production complex problems and evaluating potential impact on product quality
  • Participate in the definition of the quality requirements for projects related to e.g. process/facility/Equipment modification
  • Support any quality decision on the floor in coordination with Manufacturing.
  • Review data trending in QA perspective within his frame of responsibility ( for example Visual inspection meeting monitoring)
Quality system within his area of responsibility
  • Act as quality representative in the evaluation, the implementation and the approval of change control
  • Act as Quality Representative in the evaluation (risk evaluation, mitigations, lots potentially impacted and to be held from release), the investigation (including quality impact) and the approval of deviation Reports
Continuous improvement/Digital
  • Lead, support and/or participate to continuous improvement initiatives
  • Act as a Yellow Belt coach for projects within the department
  • Lead and/or support digital initiatives
  • Support all global initiatives related to quality related topics for the area of responsibility
  • Provide expertise during the revision of Global procedures and guidance
  • Compliance
  • Participate in external inspections.
  • Provide support if necessary to the Regulatory team by providing required data for submission files
What You Bring To Takeda
  • Master degree in Sciences (Chemist, Bioengineer, Bio statistician, Pharmacist,…)
  • 5-10years Experience in GMP environment and manufacturing environment
  • Excellent IT and digital system knowledge/capability
  • Critical thinking, stress resistant, autonomy,
  • Ability to summaries information, technical writing skills,
  • Strong communication skills,
  • Knowledge in risk management regulation, data analytics skills
  • Ability to work in a matrix organization
  • Driven by operational excellence and digital solutions
  • Focusing on priorities, handle multiple topics simultaneously in a high-volume environment, while meeting deadlines and attention to details
  • Ability to work effectively with all levels of management and resolve problems in a timely manner
  • French and English (written and spoken – advanced level) – mandatory
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.

#GMSGQ

Locations

BEL - Lessines

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

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Date limite: 10-01-2026

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