CRQA is an independent auditing and consulting firm based in Delhi, INDIA. We are an organization comprised of people specializing in Total Quality Management. We provide full range of GCP, GLP, quality assurance audits on a global basis. Our team provides a comprehensive range of quality assurance services, including auditing, consulting, SOP development and training to pharmaceutical, biotechnology and healthcare industries who are involved in Clinical research and development.
Post: QA AUDITORS-Part Time / Project Basis – All Major Cities
*Perform QA audits of clinical trial data and records in order to assure compliance with client SOPs, study protocols, GCP guidelines, relevant regulations and ISO 9000 requirements.
*Plan and conduct regular and random QA audits.
*Perform quality system audits and contract audits for Sponsors.
*Ensure that audit results are formally recorded and reported and that corrective/preventive actions are documented.
*As an auditor, perform the duties assigned in an efficient and effective manner. This includes liaison with the sponsors on all QA issues, including audit planning and review of audit results.
*Qualification in medicine, science and/or other relevant discipline and appropriate experience.
*Previous experience in Quality Assurance auditing – 2 – 5 years.
*Detailed knowledge of GCP guidelines and relevant regulations for the conduct of clinical trials.
*Ability to review and evaluate clinical data / records.
*Excellent communication and interpersonal skills.
These are part time / project assignment based positions. Only apply if you are interested in working on part time / project basis. Kindly apply in confidence with your detailed CV detailing your QA / Audit experience to firstname.lastname@example.org
LAST DATE: 30th April, 2012
See All Other Jobs in our Database