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 Auditor
- Support the application of GLP/GCP-regulations in our bioanalytical laboratories
- Auditing of study plans, raw data and reports
- Carrying out internal inspections (laboratory and general processes)
- Review of standard operating procedures
- Participation in local/global process improvement projects
Main tasks Senior Quality Assurance Auditor
- Assure GLP/GCP compliance of our bioanalytical laboratories
- Auditing of study plans, raw data and reports
- Carrying out internal inspections (laboratory and general processes)
- Review of standard operating procedures
- Participation in local/global process improvement projects
- Supporting preparation and conduct of client audits, vendor audits and regulatory inspections
- Supporting the Celerion Quality Management System
Your profile Quality Assurance Auditor
- Education in science (biochemistry, chemistry, biology, or environmental sciences)
- Work experience in the pharmaceutical or chemical industry
- Professional experience as a Quality Assurance Auditor (bioanalysis and/or GLP/GCP) is a plus
- Very good oral and written communication skills in German and English
- Attention to detail, perseverant, good IT user skills
- This position may under certain conditions also apply to entry-level applicants with proper education, without working experience
Your profile Senior Quality Assurance Auditor
- Bachelor’s degree in science (biochemistry, chemistry, biology or environmental sciences), knowledge of bioanalytical techniques
- 3-5 years’ work experience in the pharmaceutical, biotechnology or chemical industry
- 3-5 years’ professional experience as a Quality Assurance Auditor (GLP/GCP) or in another position in the area of GLP/GCP
- Knowledge of GLP/GCP regulations and/or bioanalytical guidelines (in theory and practice)
- Excellent oral and written communication skills in German and English
- Ability to organize and manage multiple priorities, excellent time management skills, attention to detail, perseverant
- Proficient IT user skills
- Occasional travel may be required
We offer
- Autonomous and varied work in an open and dynamic team
- Professional introduction to your new tasks in the GLP/GCP environment of our internationally oriented company
- Opportunity to get to know new, future-oriented technologies
- Modern Infrastructure and ergonomic workplace
- Flexible working hours, at least 5 weeks of vacation, occasional home office possible
- Gender equal Salaries, very good social benefits, REKA-Check acquisition possible
Do 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.
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Last updated on Jan 15, 2025