Senior Validation Engineer — Pharma QA & Compliance Leader

Pfizer; Rochester (MN); On-site; USD 83,000 - 138,000; Full time

Benefits offered by this job

401(k) matching

Pfizer Retirement Savings Contribution

Paid vacation, holidays and personal/m

Health benefits

Job summary

Pfizer is seeking a validation professional to join our team in Minnesota. You will evaluate and approve validation master plans, protocols, and reports, ensuring compliance with Pfizer quality standards and regulatory requirements.

Responsibilities include troubleshooting validation issues, conducting data analysis for investigations, and guiding the creation of validation documents. A strong GMP background and teamwork ability are essential for success at Pfizer.

Qualifications

• Must-have knowledge of GMP and regulatory requirements.
• Strong written and verbal communication skills.
• Experience with quality systems and document control processes.
• Ability to work independently and in a team environment.
• Penicillin facility exposure or allergy avoidance is essential.

Responsibilities

• Evaluate, review, and approve validation master plans, protocols, and reports per Pfizer quality standards.
• Troubleshoot validation issues for equipment and processes to drive resolution.
• Conduct statistical analysis of testing results and support quality investigations.
• Guide writing and approval of validation documents and technical reports.

Skills

GMP knowledge

Quality systems

Communication

Independent work

Penicillin facility familiarity

Education

High school diploma with 8+ years of experience

Associate’s degree with 6+ years of experience

BA/BS with 2+ years of experience

MBA/MS with any years of relevant experience

Tools

Global Document Management System

SAP

Quality Tracking System

Job description

Pfizer is seeking a validation professional to join our team in Minnesota. You will evaluate and approve validation master plans, protocols, and reports, ensuring compliance with Pfizer quality standards and regulatory requirements.

Responsibilities include troubleshooting validation issues, conducting data analysis for investigations, and guiding the creation of validation documents. A strong GMP background and teamwork ability are essential for success at Pfizer.