- Franklin, Ohio, United States
- On-site
- Full-time
- $69K–$114K per year
- 2+ years
Author, review, and/or approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
Compensation
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.
Responsibilities
- Author, review, and/or approve validation master plans, protocols, and reports
- 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
Requirements
- High school diploma (or equivalent) with 8+ years of experience
- Associate’s degree with 6+ years of experience
- BS with at least 2+ years of experience in pharmaceutical industry
- Nice to have: Technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems