Manufacturing Science Specialist - Contrat V.I.E.

☞ Takeda

Aussicht: 130

Update Tag: 03-12-2025

Ort: Lessines Hainaut

Kategorie: Geschäftsführung Produktion / Betrieb

Industrie: Pharmaceutical Manufacturing

Position: Entry level

Jobtyp: Full-time

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Jobinhalt

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Job Description

This position will be provided under a V.I.E contract. For more information about V.I.E contract please follow this link https //mon-vie-via.businessfrance.fr/en/what-is-the-vie-french-international-internship-program

About The Role

The Process Science Specialist handles large and complex investigations related to manufacturing processes and ensures that adequate corrective actions are implemented in a timely manner.

He defends such investigations in front of regulators. He also works on process improvements and process robustness initiatives and leads such projects from start to implementation, including the submission preparation. He leads risk analyses for existing manufacturing processes as well as for new/upgraded processes. He leads cross-functional groups (also with other facilities), evaluates possible actions to mitigate/reduce the effect of the identified risks, and ensures the follow-up of the implementation of the actions.

How You Will Contribute
  • Handles complex CAPA investigations related to manufacturing operations. In view of this
  • Uses Six Sigma and DMAIC methods where appropriate.
  • Defines tasks/experiments to be performed, provides required documentation and ensures also that adequate corrective actions are implemented to address the identified root-cause(s).
  • Ensures and defends adequate deployment, implementation and utilization of all quality systems as defined by Takeda Procedures within his organization. Ensures a thorough and timely handling of associated tasks and activities
  • Ensures and defends the Compliance to cGMP’s, GDP’s, Licenses and Takeda Procedures by defining, implementing and maintaining appropriate SOP’s and training.
  • Develops and leads projects that will improve yields, throughput & process efficiency, production process control and/or will reduce process variations. In view of this
  • Uses QbD, DIDOV, Lean and implements new technologies (including PAT) where appropriate.
  • Conducts risk analyses for existing manufacturing processes as well as for new/upgraded processes (Capacity increase, Change Request, …), evaluate and implement actions to mitigate/reduce the identified risks.
  • As a recognized process expert
  • Is involved in technology transfers, CMO related activities.
  • Ensures training of personnel on Scientific & Technical topics.
What You Bring To Takeda
  • Master or PhD degree in Pharmaceutical Sciences, Bio-Engineering or BioChemistry or equivalent by experience
  • A first experience in Pharmaceuticals & Bio-therapeutics manufacturing, in a similar function is a plus
  • Critical thinking and Problem Solving
  • GMP and bioprocessing knowledge and experience is a plus
  • Experience with Technical writing (in English) in preparation of regulatory submission files and defending topics during an FDA or cGMP audit is a plus
  • QbD, DIDOV, Lean, Six Sigma and DMAIC methods as appropriate
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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Frist: 17-01-2026

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