# Validation and Compliance Specialist- GMP/Pharma Industry at Pfizer

Pfizer is hiring a Validation and Compliance Specialist- GMP/Pharma Industry. It pays $69k-$114k a year and Level rates it Little AI ●○○○; you can [apply on Pfizer](https://jobsbylevel.com/go/556bef7e-553b-4906-9305-2bd8910b9c0d?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. United States - Ohio - Franklin.

## Details

- Company: [Pfizer](https://jobsbylevel.com/companies/pfizer)
- AI level: AI Level 1 (score 37 out of 100)
- Location: United States - Ohio - Franklin
- Salary: $69k-$114k
- Posted: November 10, 2026
- Apply: https://jobsbylevel.com/go/556bef7e-553b-4906-9305-2bd8910b9c0d?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=validation-and-compliance-specialist-gmp-pharma-industry-at-pfizer-1fad91

## Prepare for this job

The job page lists 3 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/validation-and-compliance-specialist-gmp-pharma-industry-at-pfizer-1fad91

## Description

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. What You Will Achieve In this role, you will: Author, review, and /or approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements. Perform a variety of Validation activities in compliance with Good Manufacturing Practices (GMP) and Validation Master Plan (VMP) requirements. Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities. Manage routine Quality systems such as Supplier Quality Management, Change Control, Quality Risk Management, Documentation, and Investigations, Annual Product Review and coordinate testing with functional groups. Maintain the Site Validation Master Plan and support validation as a Subject Matter Expert during customer and regulatory audits for all areas of responsibility Support regulatory queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations. Here Is What You Need (Minimum Requirements) High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BS with at least 2+ years of experience in pharmaceutical industry Proven expertise in Good Manufacturing Practices Strong working knowledge of various quality systems and processes Familiarity with information systems such as Global Document Management System, System Application & Products, and Quality Tracking System Excellent verbal and written communication skills Ability to work independently and in a team environment Bonus Points If You Have (Preferred Requirements) Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems Experience with quality management systems like Veeva and Kneat Strong analytical and problem-solving skills Strong organizational and time management skills Ability to mentor and guide other colleagues Experience in regulatory audits and compliance Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use Technical writing skills Physical/Mental Requirements Ability to perform mathematical calculations and ability to perform complex data analysis. Sitting, lifting, standing and bending. Non-Standard Work Schedule, Travel, or Environment Requirements Minimal travel requirements (less than 5%) are expected. Position requires regular onsite attendance; this position cannot be performed on a remote / telecommute basis. Other Job Details Last day to apply: November 17th, 2026. The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com).

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