QA Chemist

Pfizer; Ireland; Presencial; EUR 60 000 - 90 000; Tempo integral

Resumo da oferta

Pfizer in Ireland seeks a Quality Assurance professional to evaluate and review clinical and commercial drug batches for compliance with specifications. You will conduct sampling and SPC to identify deviations and approve investigations within cGMP frameworks.

You will collaborate with cross-functional teams, manage time on projects, and assess Change Control activities for regulatory impacts. A strong problem-solving mindset and familiarity with GxP are essential.

Qualificações

• Experience ensuring GxP compliance and regulatory standards.
• Experience reviewing clinical and commercial drug batches for compliance.
• Ability to work effectively in cross-functional teams and manage time.
• Proactive problem-solving mindset and attention to detail.
• Experience with regulatory documentation is preferred.

Responsabilidades

• Evaluate and review clinical and commercial drug batches to ensure compliance with specifications.
• Conduct sampling and statistical process control procedures to identify deviations.
• Approve investigations and change control activities to maintain cGMP compliance.
• Contribute to moderately complex projects and develop short-term work plans.
• Independently assess Change Control activities for potential QMS impacts.
• Investigate and document QA deviations and escalate when needed.
• Ensure regulatory compliance with GxP and oversee site documentation.

Conhecimentos

Strong critical thinking

Microsoft Excel

Cross-functional collaboration

Formação académica

High school diploma or equivalent

Associate's degree

Bachelor's degree (BA/BS)

Ferramentas

Microsoft Excel

GxP documentation tools

Descrição da oferta de emprego

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

• Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
• Conduct rigorous sampling and statistical process control procedures to identify deviations from standards.
• Approve investigations and change control activities to maintain compliance with configuration management policies.
• Contribute to moderately complex projects, managing time effectively and developing short-term work plans.
• Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts.
• Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
• Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

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 current Good Manufacturing Practices and relevant GxP regulations and standards
• Strong critical thinking skills
• Ability to work effectively within own team and interdepartmental teams
• Good working knowledge of Microsoft Excel and Word
• Proactive approach to problem-solving

Bonus Points If You Have (Preferred Requirements)

• Experience in quality administered systems
• Strong organizational 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, 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

Closing Date: 27th October 2026

Additional Information

In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.

Please note there is no relocation support available for this position

Purpose

Breakthroughs that change patients' lives ... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

Disability Inclusion

Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!

Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [e-mail]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

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