34 English-speaking jobs in Canton of Fribourg

  • Batmaid - CH
  • Düdingen
  • August 20
Experienced and reliable cleaners needed for part-time permanent contracts. Tasks include home, office, and end-of-tenancy cleaning. Requires cleaning industry experience and German, English, or French skills.
  • Johnson Electric International AG
  • Murten
  • August 7
Develop MBD control strategies for thermal system management, optimizing compressor modulation and energy efficiency. Responsibilities include MATLAB/Simulink modeling, MIL/HIL validation, and vehicle software integration. Requires 5-7+ years in automotive control.
  • COMET AG
  • Flamatt
  • August 7
Seeking a customer- and teamoriented Group Function Controller (80-100%). Responsibilities include financial reporting, planning, performance management, and acting as a Finance Business Partner. Requires a Finance degree and 5+ years of controlling experience.
  • COMET AG
  • Flamatt
  • August 6
Lead day-to-day operations of R&D laboratories and workshops, managing infrastructure, safety, and operational excellence. Requires a technical degree and experience in laboratory management.
  • Liebherr Group
  • Bulle
  • July 29
LogoActs as main communication partner for internal and external customers regarding diesel engines and hydraulic products. Handles complaints and warranty claims, prepares 8D reports, and conducts statistical analyses of field experience data. Approves technical statements and organizes modification actions at customer sites.
  • Sonova
  • Murten
  • July 21
LogoDevelop next-generation wireless technologies by designing and optimizing RF circuits and PCB antennas. Responsibilities include RF simulation, verification, and managing compliance for wireless communication systems. Requires a Master's degree and RF design experience.
  • UCB
  • Bulle
  • July 13
LogoGlobal Impact Quality Lead responsible for maintaining a proactive approach to pharmacovigilance compliance. Oversees PV systems, GVP/GCP guidance, and Phase IV studies. Requires 12+ years in GVP QA or Pharmacovigilance.
  • Bio-Rad Laboratories, Inc.
  • Cressier
  • July 10
LogoLead Human Factors Engineering and design validation for IVD medical devices. Conduct user research, create task analyses, and develop validation plans to ensure safety and regulatory compliance. Requires 7+ years in medical device HFE.
  • Bio-Rad
  • Cressier
  • July 10
LogoLead Human Factors Engineering and design validation for IVD medical devices. Execute user research, create design requirements, and develop validation plans to ensure safety and regulatory compliance.
  • Liebherr
  • Bulle
  • July 10
This 12-month internship supports the development of a data product foundation and a standardized data value framework. The role involves exploring data governance within the Liebherr Group, supporting the creation of a global data product framework, and identifying and evaluating the business impact of data-driven use cases.
  • Liebherr Group
  • Bulle
  • July 9
LogoInternship supporting data product foundation and building a standardized data value framework. Focus areas include data product implementation, impact estimation, and scaling valuation across divisions. Requires strong analytical skills.
  • Liebherr Group
  • Bulle
  • June 19
LogoLeads and manages GRC teams, developing and implementing the GRC strategy and framework. Oversees information security risk assessments, develops policies and procedures, and monitors compliance with regulations. Drives innovation in GRC by embedding AI and automation.
  • Liebherr Group
  • Bulle
  • June 19
LogoLeads and manages GRC teams, developing and implementing the GRC strategy and framework. Oversees information security risk assessments, develops policies and procedures, and monitors compliance with regulations. Drives innovation in GRC by embedding AI and automation.
  • UCB
  • Bulle
  • June 11
LogoThe Evidence Quality Lead ensures compliant Research, Development and Pharmacovigilance processes from candidate to commercial branding. This role develops and maintains quality strategies, identifies and manages risks, and leads compliance investigations. The ideal candidate has a Bachelor's degree in a relevant field, 10+ years in the (bio)pharmaceutical industry, and experience within the ATMP regulatory framework.
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