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QA Systems Specialist

vor 2 Wochen

Bulle FR, Freiburg, Schweiz Randstad Vollzeit
Jobdescription

Location: Bulle,Switzerland

Activity rate: 100%(non-negotiable)

Contract: temporarycontract

Start date:02.06.2025

End date:30.11.2025

UCB, one of Switzerland's BestEmployers, is an internationally active biopharmaceutical companyspecialising in the therapeutic areas of neurological disorders andimmunology. The Bulle site is home to the company's Swiss salessubsidiary and primarily a biotechnological and chemical productionplatform for the manufacture and distribution of pharmaceuticalspecialities for the treatment of allergy, epilepsy and autoimmunediseases.

To support the Quality team atUCB's Bulle site in Switzerland, we are looking for a 100% QASystems Specialist.

As a QA SystemsSpecialist, you provide strategic and operational quality systemssupport to senior management, line management, and internalstakeholders to ensure the site meets expected performance levels.You work closely at both local and global levels to proactivelysupport operations and embed high-quality standards across theorganization.

Your keyresponsibilities:

  • Strengthen thecompliance culture at Bulle site through UCB and GMPstandards
  • Actively participate in projectsrelating to Quality strategies
  • Represent theQuality Systems team internally
  • Activelycontribute to simplification and streamlining of processes andsupport continuous Quality improvementinitiatives
  • Write / approve / authorize Qualitydocumentation and maintain / improve quality systemprocedures
  • Organize and participate in Qualitycommittees
  • Help in organizing the qualitymanagement review on a quarterly basis
  • Performweekly and monthly quality systems KPIs
  • Overseegovernance, training deployment, and compliance of the process withUCB and GMP standards
  • Monitor processperformance, report issues to management, and track action plans toensure continuous improvement
  • Be responsiblefor the local process for the main quality systems (deviationsmanagement, CAPA management, investigation root causes management,QMS-Lifecycle management)
Qualifikationen

What will make yousuccessful:

  • Minimum 5 years ofprofessional experience in GMP-regulated industry, preferablywithin Quality Assurance or operationaldepartment
  • Strong autonomy, agility, andflexibility to manage multiple tasks and complex projects whilemeeting critical deadlines
  • Excellentleadership, coordination, and communication skills for effectivecollaboration
  • High level of discretion,negotiation, and persuasion abilities
  • Solidunderstanding of the GxP environment and expertise in writingscientific/technical documents
  • Proactiveapproach to improving quality processes
  • Fluentin French and English (spoken andwritten)

UCB iscommitted to fostering a diverse, inclusive, and equitableworkplace where everyone's talents and perspectives are valued andrespected.