Biotech Manufacturing Compliance Technician

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Date: Jun 6, 2019

Location: Bulle, Gruyere, CH

Help us transform patients’ lives.
At UCB, we put our heart, soul and skills into making a difference for people living with severe disease. Working together to push the boundaries, we blend the best of our talents to unlock innovation.

Will you join us in our pioneering adventure?

To strengthen our Biotech Operations Compliance team, based in our manufacturing site in Bulle, canton of Fribourg, Switzerland, we are looking to fill the position of: Biotech Operations Compliance Technician.

Do you enjoy being empathetic while keeping an analytical perspective? For UCB, this makes you an ‘empalytic’ person. This remarkable blend of talent means you are very capable of balancing sensitivity with clear thinking for the sake of patients.

As a UCB 'empalytic' person and Biotech Operations Compliance Technician you like to work in an environment where you can:

• Be the point of contact between Operations and the other functions for all quality and compliance matters

• Ensure that compliance is fully embedded in daily operation activities in the biotechnological production

• Make sure that the documentation leaving production is complete and correct

As a UCB 'empalytic' person and Biotech Operations Compliance Technician you will contribute by:
Act as primary point of contact for all compliance topics for the Operation team.

• Ensure that production documentation as batch record, raw data are reviewed according to the GMP requirements and corrected prior to transfer to QA.

• Ensure that all deviations and change request are tracked and correctly completed according to the UCB procedures. 

• Support if necessary the establishment of change control documentation and investigation report.

• Support the redaction of GMP documents as product record, procedures, reports.

• Support to establish a set of KPI to track the Compliance level of the Production activities (deviation and change management, operators training follow-up….).

• Participate to ensure that GMP rules are correctly applied during all manufacturing activities (on the field reviews, documentation reviews, discussion, internal audit, documents update…).

• Review production documentation as appropriate, to ensure proper alignment with GMP rules.

• Communicate with production teams to explain and foster compliance in daily activities. If necessary, manage training on general GMP rules.

• Support for the preparation of the health authorities and internal audits.

• Support for the follow-up of the CAPA plan issued after internal or health authority audits.

• Lead all committees related to release activities and make the link with production team and activities.

• Support the Integration of the UCB Bulle QA systems into the transversal Biotech Production organisation.


Interested? For this position you’ll need the following education, experience and skills:
• 1-3 years in Biotech manufacturing or quality.

• Knowledge of GMP and regulation linked with the Biotech manufacturing.

• High level of independence in his thinking and problem-solving activities.

• Decision-making ability and high sense of responsibility.

• Capacity for innovation.

• Ability to work under pressure and handle challenging situations.

• High communication skills.

• Fluent French and English (spoken and written).

Discover more about the remarkable UCB Talent Blends and how you can contribute to the mix at


Job Segment: Compliance, Biotech, Technician, CAPA, QA, Legal, Science, Technology, Management, Quality

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