Quality Control Biologics Specialist

Make your mark for patients

We are looking for a rigorous proactive and continuous improvement-oriented Biological Quality Control Specialist to join our Patient Supply Quality Control team based at our site in Bulle Switzerland.

About the Role

As a Biological Quality Control Specialist you will provide scientific and technical support for the laboratorys analytical activities. You will be responsible for maintaining and improving analytical methods and laboratory equipment while ensuring compliance with regulatory requirements and GMP standards. You will actively contribute to operational excellence problem-solving quality investigations and continuous improvement initiatives to support the sites competitiveness and ensure the quality of products supplied to patients.

Who Youll Work With

You will collaborate closely with Quality Control Manufacturing Supply Chain Technical Services Quality Assurance HSE and UCBs global functions. You will also interact with Analytical Development teams and Centers of Excellence to support investigations method transfers the implementation of new equipment and strategic projects related to laboratory analytical activities.

What Youll Do

• Provide technical expertise for analytical methods and laboratory equipment.
• Lead analytical investigations deviations and troubleshooting activities.
• Support the implementation of new analytical methods and laboratory equipment.
• Contribute to GMP compliance activities audits and regulatory inspections.
• Drive continuous improvement projects related to analytical processes.
• Collaborate with cross-functional stakeholders to ensure product quality.

Interested For this role we are looking for the following qualifications experience and skills:

• Masters degree in a scientific discipline or equivalent experience in the biopharmaceutical industry.
• Minimum of five years of experience in pharmaceutical or biotechnology Quality Control.
• Strong expertise in analytical techniques including ELISA bioassays HPLC UPLC and UV spectroscopy.
• Good knowledge of GMP regulations the European Pharmacopoeia USP and JP requirements.
• Experience managing investigations deviations and corrective and preventive actions (CAPAs).
• Excellent organizational leadership and communication skills with fluency in English.

Are you ready to go beyond to create value and make your mark for patients If this sounds like you then we would love to hear from you!

About us
UCB is a global biopharmaceutical company focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe inspired by patients and driven by science.

Why work with us
At UCB we dont just complete tasks we create value. We arent afraid to push forward collaborate and innovate to make our mark for patients. We have a caring supportive culture where everyone feels included respected and has equal opportunities to do their best work. We go beyond to create value for our patients and always with a human focus whether thats on our patients our employees or our planet. Working for us you will discover a place where you can grow and have the freedom to carve your own career path to achieve your full potential.

At UCB weve embraced a hybrid-first approach to work bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.