US-FL-: Quality Engineer To apply for this position, please visit this Website. http://sqa.fyicenter.com/jobs/99659599_Quality_Engineer.html To see other opportunities, please visit http://sqa.fyicenter.com Date: 04-Apr-2013
Quality Engineer * Ability to serves as a Quality resource/facilitator for audit programs including internal audits (routine and directed), external audits (e.g. FDA, ISO, etc.), supplier audit/qualification, and process validation. * Hands-on process validation experience * Experience leading/mentoring other validation professionals * Ability to support Quality Management System (e.g., facilitate change orders, CAPAs, Document control, Design Control System). * At least 2 to 5 years of experience working as a Quality Engineer; preferably in a CBER, CDER or CDRH regulated facility, required. * Must have experience with the application of the FDA’s Quality Systems Regulations (21 CFR Part 820 [especially design control requirements] and 21 CFR Part 11) and ISO quality regulations (13485 and ISO 14971). * Experience as Lead Auditor in medical device/pharmaceutical auditing practice, required. * Hands on experience with supplier auditing, qualification, and process validation, required. * Excellent oral, written and interpersonal communication skills with all internal and external customers are requiredSubject: Thank you, Team SQAFYI - Software QA Resource FYI http://sqa.fyicenter.com -- You received this message because you are subscribed to the Google Groups "Software Quality Assurance Center" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/software_qa_center?hl=en. For more options, visit https://groups.google.com/groups/opt_out.
