Quality Support Coordinator
Quality Support Coordinator
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Salary Not Disclosed
1 Vacancy
Job Description
Make your mark for patients
We are looking for a Quality Support Coordinator who is detail-oriented collaborative and proactive to join us in our Quality Manufacturing team based in our Bulle office in Switzerland.
About the role
As a Quality Support Coordinator you will support and oversee quality activities related to the manufacturing and release of Drug Substances and Bulk Drug Products. Youll play a key role in compliance continuous improvement and maintaining inspection readiness to ensure alignment with GMP standards and UCBs strategic goals.
Who youll work with
Youll be part of the Quality Manufacturing department and collaborate closely with Supply Chain Technical Services and other local and global teams. Your work will contribute to fostering a strong quality culture across departments and sites.
What youll do
- Manage quality events/deviations related to analytical laboratory (QC) activities in LIMS
- Provide quality support related to management of activities and processes related to minor deviations
- Review batch records from raw material to bulk drug product
- Coordinate and execute release activities of intermediates and components
- Support planning and execution with Supply Chain and Manufacturing
- Ensure release decisions comply with regulations and internal standards
- Contribute to SOPs and audit readiness
- Lead or support quality and process improvement initiatives
Interested For this role were looking for the following education experience and skills
- Bachelors degree or equivalent experience (e.g. CFC lab technician)
- Min. 5 years of professional experience in Quality Support
- Strong knowledge of GMP and quality release processes
- Experience with analytical testing in the Quality Control department
- Experience with Laboratory Management System (LIMS)
- Experience with batch review and regulatory documentation
- Skilled in stakeholder communication and cross-functional teamwork
- Ability to support and lead audits inspections and KPIs
- Committed to continuous improvement and quality culture development
- Candidates must be fluent in French (written and spoken)
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 around 8500 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.
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.
Required Experience:
IC
Employment Type
Full Time
