Technician, Manufacturing II (Sun-Wed, 6am to 4:30pm)

As a Technician, Manufacturing II at AbbVie, you'll be responsible for a variety of essential tasks tied to cGMP manufacturing. This includes shipping finished materials, maintaining inventory levels, sampling in-process and raw materials, and engaging in complex operations such as cell culture and tangential flow filtration. You may also be involved in preparing media and buffers, running glass washers and autoclaves, and utilizing LIMS and SAP systems for real-time data collection and adjustments.

To qualify for the Technician, Manufacturing II position at AbbVie, you need an associate's degree in a scientifically related field or equivalent experience, with at least two years of relevant manufacturing experience. Alternatively, candidates with a bachelor's degree in science or engineering are also encouraged to apply. The position requires a solid understanding of scientific principles and company policies, as well as the ability to work on semi-routine tasks with minimal supervision.

The Technician, Manufacturing II position at AbbVie operates on a Wednesday to Sunday schedule, with working hours from 6 AM to 4:30 PM. This provides a unique work-life balance that many find appealing, allowing you to complete your tasks early in the day while leaving ample time for personal activities in the evening.

In the role of Technician, Manufacturing II at AbbVie, you'll be deeply involved in various manufacturing processes including cell culture preparation, column chromatography, and filtration techniques. Your expertise will help ensure that our products meet high-quality standards, contributing to our goal of delivering innovative solutions for serious health issues.

Yes, AbbVie offers a comprehensive benefits package for the Technician, Manufacturing II role. This includes paid time off, medical, dental, and vision insurance, as well as a 401(k) plan for eligible employees. Additionally, this position may also qualify for short-term incentive programs, supporting your career growth and personal well-being.

When answering this question, focus on your knowledge of Good Manufacturing Practices and how you've applied them in previous roles. Highlight specific tasks you've managed, such as inventory control, sampling protocols, or equipment validation, to illustrate your understanding of the regulations and quality standards.

Discuss any relevant software tools you've worked with, like LIMS, SAP, or any automated control systems. Share examples of how these tools helped you collect operating data and optimize manufacturing processes, showcasing your ability to leverage technology in delivering efficiency in production.

Mention the strategies you use for task prioritization, such as assessing urgency through production deadlines or quality impact. Showcase your organizational skills and adaptability, giving examples of situations where you successfully managed multiple tasks simultaneously.

Share a specific example of a challenge, such as a production delay or quality issue. Explain the steps you took to analyze the problem, collaborate with your team, and implement an effective solution, demonstrating your problem-solving and critical-thinking abilities.

Discuss your commitment to adhering to safety and quality regulations by emphasizing regular training, staying updated on policies, and following standard operating procedures. Use past examples to illustrate how you maintain compliance in your daily tasks.

Talk about your familiarity with the calibration and maintenance of equipment used in manufacturing processes. Provide specific examples of how you've conducted routine checks or worked with engineers to ensure equipment operates efficiently and effectively.

Explain your approach to obtaining and processing quality control samples, emphasizing accuracy and attention to detail. Discuss any relevant experience you've had with sampling methodologies or handling non-conformances.

Emphasize the importance of teamwork in achieving production goals, maintaining safety standards, and fostering a culture of quality. Provide anecdotes that demonstrate how collaboration with colleagues led to positive outcomes in your previous positions.

Describe your hands-on experience with cell cultures, from the thawing process to scaling up for production. Highlight your understanding of the requirements for maintaining sterile environments and ensuring successful growth conditions.

Express your dedication to continuous learning by mentioning any professional development activities you pursue, such as attending workshops, reading industry publications, or networking with professionals. This showcases your commitment to advancing your skills in the manufacturing field.