- Bâle - 697254 - jobup.ch - Postuler - Enregistrer - Imprimer - Transmettre - - - Réf. jobup : 697254 | Date: 01/03/2012 - Senior QA Specialist - Bâle - Imagine being involved in cutting edge projects that change the course of our industry on a daily basis. At Covance, one of the world’s largest and most comprehensive drug development service companies, you will have an opportunity to build an exciting career while you make a direct impact on the lives of millions. - We are currently recruiting for a - Senior Quality Assurance (QA) auditor - based at our Phase I facility in Basel - Main responsibilities: - · Learn to verify compliance to applicable Standard Operating Procedures (SOPs) and regulations by performing internal and external audits in support of our clinical trials. - · participate in process improvement activities, assist your colleagues with the interpretation of regulatory requirements - · Represent the company during audits and inspections by our client and regulatory authorities - · Mentor less experiences QA staff - Requested profile: - · Educated to degree level or equivalent - · Minimum of 6years experience in the pharmaceutical/CRO industries, with at least 3 years in Clinical Quality Assurance, preferably within a GCP environment - · Recognized expertise in quality assurance practices - · Extensive knowledge of GCP regulatory compliance requirements is essential - · Knowledge of GMP regulatory compliance requirements is desirable - · Ability to effectively interact and communicate with all levels of scientific and management staff - Ability to independently negotiate, provide constructive feedback and support process improvement initiatives - We Offer - Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. - At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. - Experience: - - Minimum of 6(six) years experience in the pharmaceutical/CRO industry, with at least 3 (three) years in Clinical Quality Assurance within a GCP environment - Education: - Educated to degree level or equivalent - At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. - Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us. - Copy/Paste this URL into your browser to apply: http://www.applytracking.com/track.aspx/1Gool - Profil minimum requis : -