Quality Assurance Trainee

Use Your Power for Purpose

A career with us is about discovering breakthroughs that change patients whatever role you take on youll be part of bringing transformative therapies to people across the globe. Youll be at the forefront of driving the industry forward making a significant positive impact. Through your efforts youll uncover that incredible achievements are within reach. Joining us means being a crucial part of a mission to improve lives worldwide pushing boundaries and realizing that extraordinary things are indeed possible. As a member of the Global Business Services division you will play a vital role in improving patients lives while working at Pfizer.

What You Will Achieve
The Quality Assurance Intern provides support to Quality Assurance activities across Operational Quality Assurance Quality Documentation Quality Systems Quality Validations and Quality Compliance. The role contributes to GMP compliance documentation management sample retention processes complaint support activities change control documentation CAPA follow-up and regulatory monitoring.

This position offers a unique opportunity to gain hands-on experience within a pharmaceutical manufacturing environment and develop a broad understanding of Quality Systems and GMP requirements.

How You Will Achieve It

• Support implementation and maintenance of 5S principles within the QA area.

• Support review organization and filing of retain samples.

• Assist with retain sample destruction activities according to approved procedures.

• Support shipment of boxes and materials to the document storage bank.

• Participate in operational quality activities and GMP documentation support

• Support document bank management activities including requests retrievals receipts and shipments.

• Assist with Logbook management including ALCOA reviews of physical logbooks and preparation of records for archiving.

• Support preparation and maintenance of Quality Review Meeting presentations according to applicable SOPs and agendas.

• Participate in complaint-related retain sample evaluations including official photographic documentation.

• Request and coordinate retrieval of documentation from the document bank for complaint investigations.

• Support evidence required for investigation and CAPAs closure activities.

• Support validation documentation research on harmonization projects.

• Support 5S project on validation documentation room.

• Perform initial monitoring of updates to pharmacopeias and applicable regulations.

• Support tracking of CAPAs approaching their due dates.

• Assist in monitoring quality actions and maintaining critical action tracking tools.

• Contribute to compliance-related quality improvement activities.

Here Is What You Need (Minimum Requirements)

• University student pursuing a degree in Pharmacy Biochemistry Biotechnology Chemistry Engineering or a related scientific discipline.

• Strong interest in the pharmaceutical industry and Quality Assurance.

• Good organizational and documentation skills.

• Strong attention to detail and compliance mindset.

• Proficiency in Microsoft Office applications (Excel PowerPoint Word).

• Basic knowledge of statistics and data analysis is desirable.

Bonus Points If You Have (Preferred Requirements)

• Experience working in an office setting demonstrating a strong ability to adapt to various administrative tasks and environments

• Proficiency in managing office operations showcasing excellent organizational skills and attention to detail

• Familiarity with office software and technology ensuring smooth and efficient workflow

• Experience in handling confidential information with discretion and integrity

• Demonstrated problem-solving skills and the ability to think critically

• 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

• Knowledge of GMP Data Integrity principles and quality systems

Other Job Details:

• Work Location Assignment:On Premise

• Last day to apply: August 24th

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin or disability.

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