# Quality Assurance and Control

**Company**: Pfizer
**Location**: Andover, Massachusetts
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: $82,700.00 to $137,900.00
**Category**: Other
**Industry**: Healthcare

**Apply**: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---Massachusetts---Andover/QA-Specialist-III_4965935-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/quality-assurance-and-control-58da70a1-9e4/

## 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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## Skills

### Required
- Good Manufacturing Practices
- GxP regulations
- quality assurance
- Microsoft Excel
- Word
- problem-solving

### Nice to have
- quality administered systems
- regulatory compliance
- documentation
- mentoring
- AI tools
- generative technologies

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Source: [Apply at pfizer.wd1.myworkdayjobs.com](https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---Massachusetts---Andover/QA-Specialist-III_4965935-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)