Job Description

Validation Engineer III, CSV in Albuquerque, NM

The Validation Engineer III, CSV is an integral part of the Curia Quality team. This role is responsible for supporting Quality Management Systems and Computer System Validation efforts. Additionally, the Validation Engineer III, CSV will provide guidance and expertise on various global and site CSV projects to ensure that quality teams have the necessary tools to provide quality metrics, measurements, and reports for internal audits and inspections.

Essential Duties and Responsibilities:
• The main duty of the Validation Engineer III, CSV is to ensure that routine tasks related to validating electronic systems and applications used in commercial drug product manufacturing are documented in compliance with company procedures and health authority regulations.
• Generate and execute validation documents, to ensure the system(s)/software are maintained in the most current validated state per regulatory requirements
• Assist cross-functional team in identifying the required validation deliverables for new systems/software/equipment or changes to existing validated systems/software/equipment
• Assist cross-functional teams in completing system/equipment impact assessments, electronic record and electronic signature assessments
• Perform gap assessments on vendor executed protocols, ensuring compliance to current regulations are met and maintained
• Collaborate across functional areas across the organization to maintain and improve computer system validation processes to ensure robust, efficient, and compliant processes
• Provide guidance/support during specification (URS, FS, DDS or CS) document generation and review
• Shall ensure that all required Software/System Development Lifecycle Documents are available for regulatory and client audits, and participate as needed in site audits.
• Develop and execute CSV change records (Change Controls), CAPAs and Quality events for CSV projects
• Act as investigator on any CSV Deviations
• Support Site CSV actions resulting from client/regulatory audits
• Participate as site SME in site audits /inspections
• Provide guidance on quality issues that affect the integrity of data or system validation
• Maintain accurate inventory of all applications, hardware, and computer systems within the Curia Albuquerque site
• Ensure all computer systems have up to date Antivirus software and backup software installation
• Update computer systems that are running outdated Operating systems
• Investigate failed backups and investigations
• Execute periodic reviews
• Provide routine project status reports
• Provide routine software and hardware inventory updates
• Provide routine progress updates on SOPs and Templates
• Provide CAPA, QE and CR updates to compliance team
• Provide routine audit observations and remediation
• Ability to work at elevated heights
• Read/interpret SOPs to ensure compliance
• Maintain up to date trainings
• Other duties as assigned

Education and Experience:
• Bachelor's degree in Engineering, Life Science, Information Technology or related field
• Minimum of five (5) years' relevant experience working in a cGMP regulated industry specific to computer systems validation
• Validation experience in a cGMP quality control laboratory or sterile fill finish operations, developing and executing SDLC documents that meet current regulatory and industry expectation, preferred.

Supervisory Responsibilities:
This role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.

ther Skills and Abilities:
• Provides guidance and mentorship to team members
• Fosters a collaborative and positive work environment
• Champions change
• Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
• Demonstrates strong attention to detail
• Ability to adapt to changing circumstances and manage activities to meet the needs of the business while maintaining a focus on quality and information assurance.
• Solid knowledge of FDA and applicable global regulations
• Demonstrate a proactive approach to Computer System Validation
• Possess excellent leadership and management skills
• Ability to adjust quickly to shifting priorities, and decision-making skills with limited information
• Highly motivated individual with the ability to self-start, prioritize, multi-task, and has a "can-do" attitude
• Ability to communicate and work effectively with others, harness different skills and experience, and build a strong sense of team spirit
• Excellent verbal communication, and interpersonal skills to document and communicate findings, escalate critical risks to stakeholders

Other Qualifications:
Must pass a background check
Must pass a drug screen
May be required to pass Occupational Health Screening
May be required to obtain and maintain gowning certification
May be required to obtain and maintain media qualification
May be required to wear a respirator

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address.