2025 Quality Assurance-PQA Co-Op (June - December)

As a 2025 Quality Assurance-PQA Co-Op at AbbVie, your primary responsibilities include supporting the Quality Assurance department by troubleshooting compliance issues, performing site walk-throughs, and assisting with various quality-related projects. You will be involved in ensuring manufacturing conformity to AbbVie's quality standards and regulatory requirements, providing you with hands-on experience in the pharmaceutical industry.

To qualify as a 2025 Quality Assurance-PQA Co-Op at AbbVie, you should be currently enrolled in a university program pursuing a degree in chemical engineering, biochemistry, biology, or a related field. Moreover, it's essential that you plan to enroll for at least one semester after completing the Co-Op, with an expected graduation date ranging between May 2026 and May 2027.

The 2025 Quality Assurance-PQA Co-Op at AbbVie offers a remarkable opportunity to gain real-world experience and build your resume in the pharmaceutical sector. You'll enhance your skills in quality assurance practices, compliance procedures, and teamwork with experienced professionals. This Co-Op position provides you with networking opportunities, valuable mentorship, and potential pathways to future employment within the company.

Essential skills for a 2025 Quality Assurance-PQA Co-Op at AbbVie include strong attention to detail, effective communication abilities (both verbal and written), and proficiency in basic office software like Microsoft Office. Familiarity with electronic document management systems and knowledge of GMP regulations would also greatly benefit candidates in this role.

In the work environment of a 2025 Quality Assurance-PQA Co-Op at AbbVie, you can expect a collaborative and inspiring atmosphere. You'll work with energetic colleagues and inspirational leaders who are dedicated to continuous improvement and employee development. The culture emphasizes innovation, integrity, and making a positive impact on people's lives.

Quality assurance in the pharmaceutical industry focuses on ensuring that products meet safety and efficacy standards. Understanding how regulatory compliance, Good Manufacturing Practices (GMP), and quality management systems operate is essential. Discuss how these elements work together to prevent defects and ensure patient safety.

Troubleshooting quality issues involves a systematic approach: identifying the problem, gathering data from relevant sources, analyzing defects or deviations, and developing potential solutions. Discuss examples of how you've used this problem-solving method in academic settings or past experiences.

I am very proficient in Microsoft Office tools such as Word, Excel, and PowerPoint, using them for data analysis, project tracking, and presentations. Share specific instances where you utilized these tools effectively, such as creating visual reports or organizing team tasks.

Key qualities for a Quality Assurance Co-Op include attention to detail, effective communication, adaptability, and a strong sense of ethics. These traits ensure high compliance and quality standards are maintained while fostering collaboration within the team.

In one challenging team project, I took on the role of a coordinator, organizing tasks, ensuring open communication, and managing deadlines. Detail how you navigated obstacles and contributed to the team's success, demonstrating teamwork and leadership skills.

When prioritizing multiple projects, I assess deadlines, importance, and potential impact. Using tools like to-do lists or project management software helps me stay organized, ensuring I allocate time appropriately to each task, ultimately meeting all deadlines.

I have theoretical knowledge of electronic document management systems from coursework and am eager to gain practical experience. Discuss your willingness to learn and adapt to new technologies, as well as your meticulous approach to managing documentation.

Regulatory compliance is critical in quality assurance as it ensures that products meet industry standards for safety and efficacy. Discuss the implications of non-compliance and how it can affect patient safety and company reputation, underscoring its importance in the pharmaceutical sector.

I would break down the issue into simple terms, using analogies or visuals to ensure clarity. Emphasizing the impact and resolution process helps convey the message effectively without losing the audience in technical jargon.

I am drawn to the Quality Assurance Co-Op position at AbbVie because of the company's commitment to innovation and excellence in healthcare. This role aligns perfectly with my academic background and my aspiration to make a meaningful contribution to quality and compliance in the pharmaceutical industry.