Manager Manufacturing - Purification

☞ Takeda

Visualizza: 125

Giorno di aggiornamento: 16-11-2025

Località: Lessines Hainaut

Categoria: Consiglio di amministrazione Produzione / Funzionamento

Industria: Pharmaceutical Manufacturing

Posizione: Mid-Senior level

Tipo di lavoro: Full-time

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Contenuto del lavoro

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Job Description

Aboutthe role

The Purification Manager is responsible for managing the manufacturing operations of his Purification Line (depending on the Purification Line, products can be amongst others Glassia, Gammagard Liquid/Kiovig, Gammagard S/D, Cuvitru) in line with the Takeda Business Strategy Plan.

How You Will Contribute
  • Guarantee the output of Purification Line assuring the respect of the quality, production schedule and standard cost;
  • Ensure strict compliance with cGMP, 21 CFR’s, Corporate, Divisional and regulatory requirements;
  • Promote individuals in technical, organizational and management fields
  • Manage a multi-shift production team, ensuring resource availability, and developing staff, fostering a culture of continuous improvement
  • Strongly support the Takeda culture in Ethics, Compliance and EHS.
  • Drive the deployment of the Continuous Improvement (CI) culture across his field of responsibilities; responsible for the good execution of the project portfolio on his Manufacturing Line.
  • Ensure production commitments are met, implement lean manufacturing processes, report KPI’s (Quality, Supply Chain, EHS), facilitate process improvements and fosters team development and flexibility.
What You Bring To Takeda
  • Bachelor’s in Biochemistry/Science/Bio-Engineering or higher degree (Master/Ph.D)
  • Minimum 5 years in a position of Manufacturing/Manufacturing Sciences/Process Engineering
  • Management skills leadership, assertive, stress resistant, flexibility, integrity, communication, excellent manager for himself and for the team
  • Outstanding communication skills, be able to interact with manufacturing teams, internal and external customers and regulatory bodies
  • Capacity to federate the services interacting with Manufacturing (i.e. Quality, Supply Chain) in order to achieve manufacturing or site objectives.
  • Mastering DMAIC methodology and associated statistical tools
  • Fluent in French and English (both oral and written)
  • Computer skills Microsoft Office Programs (Word, Excel, PowerPoint), JDE, Minitab, SQ LIMs, Critical Farm Citrix (OSIPI)
  • Experience with Lean Six Sigma tools and Project Management skills
  • Experience with troubleshooting and problem solving with process and equipment
  • Experience with automated process equipment and control
  • Broad technical knowledge in Purification and more specifically in production capacity modelling
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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Scadenza: 31-12-2025

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