Pfizer
SupplyOperationsQualityAssociate
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Supply Operations Quality Associate at Pfizer. Skills: Quality investigations, Compliance issues, SOP review, CAPA assistance. Contribute to projects by managing time. Plan short-term work activities”
What You'll Achieve.
Resolve compliance issues in the marketplace; Identify trends in inquiry data; Enhance quality
Industry & Context.
Analyze inquiry data to identify trends; Suggest modifications to enhance quality; Analyze and interpret data to identify trends; Support problem solving
Fixed term period of 12 months
What They're Looking For.
Must Have
High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BAS with 2+ years of experience or MBA/MS with any years of relevant experience, Solid understanding of regulatory GDP/GMP compliance issues related to the manufacturing and distribution of medicinal products, Excellent organizational skills and the ability to juggle multiple priorities, collaboration, communication, and interpersonal skills to work effectively with local, regional, and global colleagues, Proficiency in using System Application and Products, and Microsoft Office Suite, Technical expertise to handle complex quality assurance and control tasks
Nice to Have
Relevant pharmaceutical experience, particularly in the use of Electronic Quality Management Systems, Supervisory experience, Knowledge of complaint processing systems and the ability to suggest modifications to enhance quality, Experience in facilitating product-focused training sessions, Ability to analyze and interpret data to identify trends and communicate findings, Excellent judgment and decision-making skills, Ability to mentor and review the work of other colleagues, Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
What You'll Do.
Contribute to projects by managing time
Plan short-term work activities
Lead product quality investigations
Follow up on actions to resolve compliance issues
Serve as Subject Matter Expert
Review Standard Operating Procedures (SOPs)
Analyze inquiry data to identify trends
Assist with audit Corrective & Preventive Actions (CAPAs)
Review documentation related to repackaging and relabeling
Compile Key Performance Indicator figures
Facilitate product-focused training sessions
How You'll Work.
Team & Collaboration
Work effectively with local, regional, and global colleagues
Communication Scope
Communication skills
Process & Methodology
Manage time effectively, Plan short-term work activities
Full Job Description
**This role has a fixed term period of 12 months.** **Use Your Power for Purpose** Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. **What You Will Achieve** In this role, you will: * Contribute to moderately complex projects by managing your time effectively and planning short-term work activities. * Lead product quality investigations and follow up on actions to resolve compliance issues in the marketplace. * Serve as a Subject Matter Expert and reviewer for Standard Operating Procedures (SOPs) and analyze inquiry data to identify trends. * Assist with audit Corrective & Preventive Actions (CAPAs), review documentation related to repackaging and relabeling, compile Key Performance Indicator figures, and facilitate product-focused training sessions. **Here Is What You Need**(Minimum Requirements) * High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience * Solid understanding of regulatory GDP/GMP compliance issues related to the manufacturing and distribution of medicinal products * Excellent organizational skills and the ability to juggle multiple priorities * Strong collaboration, communication, and interpersonal skills to work effectively with local, regional, and global colleagues * Proficiency in using System Application and Products, and Microsoft Office Suite * Technical expertise to handle complex quality assurance and control tasks **Bonus Points If You Have**(Preferred Requirements) * Relevant pharmaceutical experience, particularly in the use of Electronic Quality Management Systems * Supervisory e
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