Description
We are seeking a Validation Engineer to join our team at the Pfizer PGS Pearl River site.
The successful candidate will be responsible for the effective implementation, execution, and sustaining of site Continuous Improvement projects and Validation Master Plan Program Elements for clean utilities and equipment cleaning.
Key responsibilities include:
- Developing and executing cleaning validation, clean utility equipment qualification, protocols, and reports to support the site master plan execution
- Authoring, reviewing, and approving technical reports and development studies to support clean utilities and equipment cleaning and equipment projects
- Managing project milestones to support new process, technology transfer, or equipment installations in collaboration with Operations, Opex, and Engineering
- Coordinating with vendors and contract resources to ensure compliance with Pfizer standards
- Participating in PCT operational huddles and shift huddles
- Supporting regulatory/internal audits
Requirements:
- Associate's degree with 5+ years of experience or Bachelor's degree with 2+ years of experience in a related field
- Strong knowledge of cGMP and FDA rules and regulations
- Excellent organization and time management skills
- Ability to effectively collaborate with team members within and across functions
- Proficiency in data analysis and trend monitoring
- Experience using common AI tools
Benefits:
- Comprehensive and generous benefits package, including 401(k) plan with Pfizer matching contributions, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits
- Annual base salary ranging from $82,700 to $137,900
- Eligibility for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% of the base salary