Pfizer

Pfizer

Posted via Workday

Senior QA Validation Specialist

Apply by Sep 19, 2026

Posted Sep 17, 2026

Role at a glance

Job function
Manufacturing & Skilled Trades Quality Assurance & Quality Control
Salary
Not Disclosed
Location
Mulgrave, Victoria, Australia
Work arrangement
On-site
Employment
Full-time
Experience
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...
Education
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...

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Role Summary

AI-generated

This role supports engineering validation and quality activities for pharmaceutical products and processes at an on-premise site. The position maintains validation documentation and systems, supports audits and investigations, and contributes to product transfers, new product development, and process improvement.

What You'll Do

  • Evaluate, review, and approve validation master plans, protocols, and reports.
  • Troubleshoot validation issues for equipment and performance processes.
  • Conduct statistical analysis of testing results and process anomalies for Quality Investigations.
  • Guide the writing, review, and approval of validation process documents and technical reports.
  • Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations.
  • Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams.

Generated from the employer's posting. Verify important details before applying.

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Qualifications

Minimum requirements include expertise in Good Manufacturing Practices, knowledge of quality systems and processes, familiarity with Global Document Management System, System Application & Products, and Quality Tracking System, strong communication skills, and the ability to work independently and in a team environment.

Required

  • Good Manufacturing Practices
  • Quality systems and processes
  • Global Document Management System
  • System Application & Products
  • Quality Tracking System
  • Excellent verbal and written communication skills

Preferred

  • Validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems
  • Sterile products and medical devices
  • Regulatory audits and compliance
  • Common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot
  • Responsible AI practices, including risk management and ethical use

Original job description

Content provided by the employer

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.

What You Will Achieve

In this role, you will:

  • Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
  • Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.
  • Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.
  • Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.
  • Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.
  • Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations, and coordinate testing with functional groups.
  • Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams.
  • Support product transfers, new product development, regulatory queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations.

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  
  • Proven expertise in Good Manufacturing Practices
  • Strong working knowledge of various quality systems and processes
  • Familiarity with information systems such as Global Document Management System, System Application & Products, and Quality Tracking System
  • Excellent verbal and written communication skills
  • Ability to work independently and in a team environment

Bonus Points If You Have (Preferred Requirements)

  • Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems
  • Experience with sterile products and medical devices
  • Strong analytical and problem-solving skills
  • Strong organizational and time management skills
  • Ability to mentor and guide other colleagues
  • Experience in regulatory audits and compliance
  • 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
  
Work Location Assignment: On Premise

At Pfizer we care about our colleagues’ wellbeing and offer a range of great benefits for them, including:

  • Paid parental leave

  • Access to Health & Wellness apps

  • Career Growth Experiences program

  • Recognition & rewards program

  • Paid volunteer days

  • Life Insurance Benefits

  • Pfizer Learning Academy access to top content providers

  • Access to flu vaccines & skin checks

  • Options to purchase additional leave

  • Salary packaging & novated lease options

*Benefits listed may vary depending on your position and location and may be subject to change.

Pfizer Australia and New Zealand’s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.

If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.


To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

 

 

Quality Assurance and Control


Pfizer

About the company

Pfizer

Large Enterprise

Pfizer is a global biopharmaceutical company dedicated to the discovery, development, and manufacturing of innovative healthcare solutions. With a strong focus on improving lives through medications and vaccines, Pfizer has played a significant role in addressing various health challenges, including infectious diseases, chronic illnesses, and rare conditions. The company emphasizes research-driven approaches and collaborative efforts in its mission to enhance global health and empower patients through cutting-edge science and technology. Through its commitment to high standards of safety and efficacy, Pfizer continues to shape the future of medicine.