"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.
Your Role:
Lead Quality Where It Matters MostIf you've built your career in pharmaceutical manufacturing and enjoy leading people, developing teams, solving problems in real time, and being where the action happens, we'd love to meet you.As the QA Operations Supervisor, 2nd Shift, you'll lead a team of QA professionals supporting sterile and aseptic manufacturing operations while serving as the primary Quality leader on the production floor. Working closely with Manufacturing, Validation, Engineering, and Microbiology, you'll help ensure products are manufactured safely, consistently, and in compliance with cGMP requirements. Every decision you make helps support our clients and the patients who rely on the treatments we produce.This is a hands-on, onsite leadership role for someone who thrives in a fast-paced GMP environment, enjoys coaching and developing others, and takes pride in building a strong culture of quality, compliance, and patient focus. You'll spend much of your time on the manufacturing floor partnering with Operations, supporting production activities, and providing real-time quality oversight where it matters most.Your Profile:
Lead and develop a team of Quality professionals supporting sterile manufacturing operations
Serve as the primary Quality leader for a critical production shift
Join a growing pharmaceutical CDMO committed to quality, innovation, and continuous improvement
Partner closely with Manufacturing, Engineering, Validation, Microbiology, and Site Leadership
Gain valuable exposure to client programs, regulatory inspections, and complex sterile manufacturing operations
Make a direct impact on product quality, compliance, operational performance, and patient safety every day
Onsite leading the 2nd Shift Team: 2:00 PM - 10:30 PM
Target Salary Range: $80,000 - $95,000 annually
Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications, and other job-related reasons.
Apply today and bring your Quality leadership expertise to a team where your impact can be seen in every shift, every batch, and every treatment we help deliver to patients.
Your Benefits:
Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.
| Location | Irvine, California |
| Salary | $80,000–$95,000 Per Year |
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