Validation Lifecycle & Periodic Review Specialist

Validation Lifecycle & Periodic Review Specialist

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas:
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

• Validation Lifecycle & Periodic Review Specialist

Location:

Hybrid

We are seeking a Validation Lifecycle & Periodic Review Specialist to support our client in maintaining validated systems throughout their lifecycle. This role is responsible for supporting validation lifecycle and periodic review activities for GMP equipment, facilities, utilities, controlled temperature chambers, computerized systems, and associated validation maintenance activities.

The successful candidate will support the execution of assessments and reviews to ensure systems remain compliant, fit for intended use, and maintained in a validated state throughout their lifecycle.

• Support execution of validation lifecycle and periodic review activities for GMP systems.
• Perform Equipment Periodic Reviews (EQPRs), Controlled Temperature Chamber Reviews (CTCPRs), Computerized System Periodic Reviews (CSPRs), and Annual Audit Trail Reviews (AATRs), as applicable.
• Gather and review maintenance, calibration, deviation, change control, CAPA, and system performance information.
• Support assessments of system changes and their impact on validation status and compliance requirements.
• Assist in evaluating systems for continued suitability, compliance, and validated state.
• Author and revise periodic review reports and associated validation lifecycle documentation.
• Support development, maintenance, and updates of Validation Master Plans (VMPs).
• Support Annual Product Review (APR) activities and summary reports.
• Participate in cross-functional discussions with Engineering, Quality, Operations, Maintenance, Automation, and Validation personnel.
• Identify and communicate potential compliance risks, gaps, and improvement opportunities.
• Support regulatory inspections, audits, and client requests, as required.

• Bachelor's degree in a technical, scientific, quality, compliance, engineering, or related discipline.
• Minimum 2 years of experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Experience supporting GMP systems, quality systems, validation programs, compliance activities, or related technical functions.
• Experience authoring, reviewing, or supporting GMP documentation.
• Understanding of validation lifecycle concepts, quality systems, and GMP compliance requirements.
• Strong technical writing, organizational, and communication skills.
• Ability to manage multiple assignments and priorities in a fast-paced environment.

• Experience supporting one or more of the following:
  Equipment Periodic Reviews (EQPR), Controlled Temperature Chamber Reviews (CTCPR), Computerized System Periodic Reviews (CSPR), Annual Audit Trail Reviews (AATR), Annual Product Review (APR) support, Data Integrity Assessments, Change Control and Deviation Management, Validation Maintenance Programs.
• Experience with Maximo, Track Wise, Kneat, CDOCS, Service Now, or similar systems.

At Validation & Engineering Group, people always come first. We believe that when you’re empowered to do your best work, bold ideas thrive and real progress happens. This isn’t just a job – it’s an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.