QA Auditor II/III (Vendor Auditor)

Work Schedule Other Environmental Conditions Office Job Description Join us as Quality Assurance Auditor II - And enhance our clinical auditing processes by ensuring regulatory compliance and quality standards. What You’ll Do: Conduct and/or lead a variety of GxP qualification and routine vendor audits, as requested by senior management, including but not limited to on-site, virtual and remote audits of service providers used in clinical trials with or without technology components • Perform directed vendor audits • May perform clinical investigator site Provide GxP consultation and support to internal and external clients • Serve as a knowledgeable resource to operational departments on audit or quality assurance subject matter • Prepare and present audit findings and/or other related information at departmental, internal operations or client meetings Education and Experience: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous QA and GxP vendor auditing experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years’). • Fluent in English, Spanish and Portuguese In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: Solid knowledge of the clinical trial process Thorough knowledge of GxP and appropriate regional research regulations and guidelines • Demonstrated proficiency and led a range of GxP vendor audits to high standards required by management • Excellent oral and written communication skills (including appropriate use of medical and scientific terminology) • Strong attention to detail Effectively works independently or in a team environment • Highly developed problem solving, risk assessment and impact analysis abilities • Solid experience in root cause analysis and CAPA development • Above average negotiation and conflict management skills • Proven adaptability Strong organizational and time management skills including flexibility and ability to multi-task and prioritize competing demands/workload • Strong computer skills; ability to learn and become proficient in appropriate systems Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel The following is a plus: Experience performing other types of QA audits or activities (e.g., investigator site audits, database audits, clinical study report audits, sample results tables, process improvement) • Experience hosting client audits and/or regulatory inspections. • Experience delivering training. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthrough. Originally posted on Himalayas