QA Validation Specialist III

Pfizer seeks a QA Validation Specialist III for its Andover, Massachusetts site to oversee validation programs and ensure pharmaceutical products meet quality and safety standards. The role involves reviewing validation documentation, change controls, and investigations while maintaining compliance with regulatory requirements.

Responsibilities

• Provide quality assurance oversight for the validation program at the Andover site
• Review and approve validation documentation including specifications, protocols, reports, and plans
• Review and assess change controls for validation impact and required testing
• Support project teams on compliance and technical validation issues
• Review and approve investigations, commitments, and maintenance work orders related to validation

Requirements

• Bachelor's degree with 4+ years relevant experience, or equivalent education/experience combination
• Strong understanding of validation principles and practices in pharmaceutical settings
• Knowledge of regulatory requirements and validation guidelines
• Proficiency in project management and resource planning
• Ability to work independently and make decisions in ambiguous situations
• Proficiency with computerized systems and software applications
• Excellent communication and interpersonal skills

Compensation: $82,700–$137,900 base salary plus 10% bonus target