Position: Mid-Senior level

Job type: Full-time

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Job content

To strengthen our Quality Operations department, based in our manufacturing site in Bulle, Switzerland, we are looking for a talented individual to fill the position of: Quality Operations Coordinator.

As a Quality Operations Coordinator for the Raw-Material,you will be responsible for coordinating release activitieswith regards to the operations, planning related to the external products (Solvents, Chemical & Pharmaceutical Raw Materials, purchased APIs) in compliance with national and/or international regulations, Pharmacopoeia, guidelines (GMP), relevant UCB Quality Policies.

You like to work in an environment where you can:

  • Have a diversity of activities on the field.
  • Collaborate with different internal stakeholders from manufacturing, Supply Chain, Technical Services, Quality & HSE Compliance and Business Acceleration departments.
  • Proactively support operations (on the floor) in order to identify, develop, and implement quality and operational excellence improvements in response to business requirements and/or technical changes and/or regulatory requirements.
  • Actively contribute to simplification and streamlining of processes to remove unwanted roadblocks and support continuous quality improvements.
  • Take an active role in the follow-up of Quality items.

Responsibilities - You will contribute by:

  • Being responsible for the review of batch records related to the external products (Solvents, Chemical & Pharmaceutical Raw Materials, purchased APIs).
  • Being responsible for the release activity of external products, released by QC.
  • Managing in close cooperation with Manufacturing, Supply Chain and QOPS Team Leader the analysis and release planning.
  • Participating to laboratory organization.
  • Managing the Deviations, Investigations, CAPAs.
  • Assessing the quality of batches to assure the release is carried-out according to regulations and UCB standards/procedures.

Interested? For this position you’ll need the following education, experience and skills:

  • Minimum of 4 years professional experience in manufacturing, laboratory, development, quality control or quality assurance.
  • Demonstrated understanding of GMP environment.
  • Education: Bachelor in Life Sciences / CFC of laboratory technician or equivalent.
  • Strong analytical and investigations skills.
  • Ability to meet/respect critical deadlines.
  • Strong teamwork and collaboration skills.
  • Ability to plan and prioritize.
  • Capacity to make decisions.
  • Excellent communication skills (both oral and written).
  • Demonstrate negotiation and convincing skills.
  • Demonstrated ability to write-up scientific/technical documents.
  • Developed sense of discretion, precision and responsibility.
  • Languages: French, English (both writing and speaking).

Why you should apply

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.

If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

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Deadline: 10-05-2024

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