Description
At Pfizer, you will contribute directly to patients by ensuring the delivery of safe and effective products.
What You Will Achieve
In this role, you will:
- Provide guidance, lead or co-lead projects for digital solutions
- Routinely provide updates to the team and management on project milestones
- Independently support complex investigations in cross-functional work areas, providing sound quality assurance judgment to ensure product quality as needed
- Work in a fast-paced environment, juggling priorities as required
- Review and approve electronic records, protocols, and reports, and author, review, and approve SOPs as needed
- Independently provide Quality Review and oversight of site documentation to ensure compliance with global regulatory agencies and Pfizer quality standards
- Collaborate with a wide range of co-workers, customers, and management to gather input and background knowledge
- Anticipate issues and provide recommendations for path forward to management attention
- Review and approve change controls as needed
- Exercise judgment in resolving complex quality issues
- Plan and execute work independently, consulting with supervisor as needed
- Apply technical and quality concepts, applicable guidelines, and SOPs
- Lead and drive continuous improvement activities
- Proactively apply sound technical judgment to resolve quality issues
- Drive effective management of quality issues and Corrective Action Plans (CAPAs)
Here Is What You Need
- High school diploma or equivalent with 8+ years of experience, associate's degree with 6+ years of experience, or BA/BS with 2+ years of experience
- Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards
- Experience in a GMP manufacturing or GMP Quality Assurance role
- Strong critical thinking skills
- Ability to work effectively within teams and interdepartmental teams
- Good working knowledge of Microsoft Excel and Word
- Proactive approach to problem-solving
Bonus Points If You Have
- Experience in quality administered systems
- Strong organisational skills and attention to detail
- Experience with regulatory compliance and documentation
- Ability to mentor and review the work of other colleagues
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot
Other Job Details:
- Work Location Assignment: Hybrid
- Relocation Assistance Available: NO
- Last date to apply: 11/13/2026
- Annual base salary: $82,700.00 to $137,900.00
- Eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% of the base salary
- Comprehensive benefits and programs, including 401(k) plan, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits
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