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 youll 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 youll 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 followup in collaboration with Quality and subject matter experts.
• Coordinate and support internal audits and inspections including preparation documentation readiness and followup 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 valueadding solutions.

Interested For this role were looking for the following education experience and skills

• Bachelor or Master in Life Sciences.
• Experience working in a GMPregulated pharmaceutical or manufacturing environment.
• Solid understanding of GMP compliance documentation management deviations CAPAs and audits.
• Ability to work crossfunctionally 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 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.