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 providing 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 to receiving 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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