Validation & IT Auditor II

CTI, Inc.
Covington, United States of America
18 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Intermediate
Compensation
$ 75K

Job location

Remote
Covington, United States of America

Tech stack

Software as a Service
Computer Telephony Integration

Job description

  • Conduct internal audits related to validated systems and IT processes. Escalate any unresolved observations to QA management
  • Conduct vendor audits of SaaS vendors to assess qualification status. Escalate any unresolved observations to QA management
  • Prepare and distribute audit reports, providing clear communication of audit observations of the relevant CTI leadership.
  • Assist with review of auditee response plans for adequacy of corrective and preventive actions and follow through to effective resolution.
  • Assist QA leadership team with review of non-conformance root causes and implementation of effective corrective actions related to IT processes, clinical systems and validation CAPAs.
  • Assist with review, revision, and management of IT, validation and system related SOPs
  • Assist QA leadership team with validation improvement initiatives
  • Provide guidance as needed for risk assessments and/or ensuring procedural controls are in place to mitigate risk and maintain compliance
  • Assist with implementing tools and procedures to facilitate documentation and tracking of quality assurance validation audit activities.
  • Maintain significant knowledge in global regulatory validation requirements to provide regulatory compliance guidance and quality improvement consult to internal functions; proactively maintain in-depth knowledge of 21 CFR Part 11 Compliance
  • Assist with preparing training materials related to global validation requirements
  • Assume administrator responsibilities for quality assurance electronic systems. Create new accounts and assign appropriate roles/access.
  • Recommend changes to current processes to provide more effective use of the quality assurance electronic systems and take the lead to implement such changes
  • Prepare training materials and conducting training related to relevant QA topics for CTI staff
  • Create and format document templates & trackers
  • Work closely with QA leadership to learn and enhance Quality Assurance responsibilities

Requirements

  • Bachelor's degree in business administration or physical/life science
  • Documentation of exceptional performance in prior leadership role(s)
  • At least 4 years in CRO, pharmaceutical, clinical or related fields

Benefits & conditions

Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department. * Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program. * Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

About the company

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

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