Compliance Specialist

Make your mark for patients

We are looking for a Compliance Specialist, who is eager to join our site Technical Support department, based in our manufacturing site in Bulle, Switzerland.

About the role

We are looking for a Compliance Specialist to strengthen GMP compliance across Technical Services and Manufacturing Support departments.

In this role, you will play a key part in maintaining a high level of GMP compliance across Technical Services and Manufacturing Support and take ownership of compliance and documentation activities. Working closely with Quality and operational teams, you will help strengthen a culture of quality, ownership, while supporting inspections, audits, and continuous improvement initiatives.

Who you’ll work with

You will collaborate closely with Technical Services and Manufacturing Support teams, Quality partners, subject matter experts, and site stakeholders. You will also interface with auditors and inspectors as part of your compliance support responsibilities.

What you’ll do

• Ensure compliance of Technical Services and Manufacturing Support processes, activities, and documentation with GMP, regulatory, and internal requirements.


• Act as a compliance and documentation partner for department management, providing guidance and operational support.


• Support deviations, investigations, and CAPA follow‑up in collaboration with Quality and subject matter experts.


• Coordinate and support internal audits and inspections, including preparation, documentation readiness, and follow‑up of action plans.


• Manage training and competence matrices, ensuring alignment between roles, activities, and GMP training requirements.


• Contribute to continuous improvement initiatives by proposing pragmatic, compliant, and value‑adding solutions.

Interested? For this role we’re looking for the following education, experience and skills

• Bachelor or Master in Life Sciences.


• Experience working in a GMP‑regulated pharmaceutical or manufacturing environment.


• Solid understanding of GMP compliance, documentation management, deviations, CAPAs, and audits.


• Ability to work cross‑functionally with diverse stakeholders in a regulated environment.


• Strong organizational skills, with a structured and analytical approach.


• A proactive, collaborative mindset with a strong sense of ownership and accountability.


• Clear and effective communication skills in French and 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 don’t just complete tasks, we create value. We aren’t 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 that’s 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, we’ve 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 [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.