Celerion is one of the world's leading companies in bioanalytical contract research and has been supporting pharmaceutical and biotech companies around the world for more than 40 years. Celerion provides regulatory services for new drugs - from early development to clinical trials - and is committed to provide patient support as fast as possible. To strengthen our Quality Assurance team we are looking for an experienced, committed and motivated person for our bioanalytical site in Fehraltorf (Zurich area) Switzerland for the position

 (Senior) Quality Assurance Auditor 100%Main tasks Quality Assurance AuditorSupport the application of GLP/GCP-regulations in our bioanalytical laboratoriesAuditing of study plans, raw data and reportsCarrying out internal inspections (laboratory and general processes)Review of standard operating proceduresParticipation in local/global process improvement projectsMain tasks Senior Quality Assurance AuditorAssure GLP/GCP compliance of our bioanalytical laboratoriesAuditing of study plans, raw data and reportsCarrying out internal inspections (laboratory and general processes)Review of standard operating proceduresParticipation in local/global process improvement projectsSupporting preparation and conduct of client audits, vendor audits and regulatory inspectionsSupporting the Celerion Quality Management SystemYour profile Quality Assurance AuditorEducation in science (biochemistry, chemistry, biology, or environmental sciences)Work experience in the pharmaceutical or chemical industryProfessional experience as a Quality Assurance Auditor (bioanalysis and/or GLP/GCP) is a plusVery good oral and written communication skills in German and EnglishAttention to detail, perseverant, good IT user skillsThis position may under certain conditions also apply to entry-level applicants with proper education, without working experienceYour profile Senior Quality Assurance AuditorBachelor’s degree in science (biochemistry, chemistry, biology or environmental sciences), knowledge of bioanalytical techniques3-5 years’ work experience in the pharmaceutical, biotechnology or chemical industry3-5 years’ professional experience as a Quality Assurance Auditor (GLP/GCP) or in another position in the area of GLP/GCPKnowledge of GLP/GCP regulations and/or bioanalytical guidelines (in theory and practice)Excellent oral and written communication skills in German and EnglishAbility to organize and manage multiple priorities, excellent time management skills, attention to detail, perseverantProficient IT user skillsOccasional travel may be requiredWe offerAutonomous and varied work in an open and dynamic teamProfessional introduction to your new tasks in the GLP/GCP environment of our internationally oriented companyOpportunity to get to know new, future-oriented technologiesModern Infrastructure and ergonomic workplaceFlexible working hours, at least 5 weeks of vacation, occasional home office possible Gender equal Salaries, very good social benefits, REKA-Check acquisition possibleDo you have questions? Your contact person Iris Rüttimann (HR Manager) is always available on +41 43 355 7676.
We want to get to know you! We are looking forward getting your application!

Information for recruiting agencies: Celerion only accepts direct applications for this vacancy. Unfortunately, we cannot consider dossiers from employment agencies.