Quality Assurance Operations Supervisor, Pharmaceutical Manufacturing - 2nd Shift

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.

If 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.

• Supervise, mentor, and develop a team of QA Technicians and QA Associates supporting second‑shift operations.
• Manage shift staffing, work assignments, priorities, and shift handoffs.
• Provide coaching and leadership that strengthens quality culture, accountability, and team performance.
• Foster a collaborative environment focused on continuous improvement and operational excellence.

• Provide real‑time quality oversight for formulation, compounding, filling, visual inspection, and packaging activities.
• Perform in‑process verifications, line clearances, operational observations, and batch record reviews.
• Maintain an active presence on the manufacturing floor to ensure compliance with cGMP requirements, SOPs, data integrity principles, and sterility assurance practices.
• Observe aseptic techniques, gowning practices, and critical interventions to support product quality and patient safety.

• Support investigations, deviations, CAPAs, and root cause analysis activities.
• Evaluate quality events and partner cross‑functionally to resolve issues and drive sustainable improvements.
• Promote Right‑First‑Time documentation practices and ALCOA+ data integrity principles.
• Monitor quality performance and identify opportunities to strengthen compliance and operational effectiveness.
• Support a culture of continuous inspection readiness.

• Serve as a Quality representative during client audits, customer visits, and regulatory inspections.
• Partner with Manufacturing, Engineering, Validation, Microbiology, and Quality Systems teams to maintain compliance and support operational excellence.

• Bachelor's degree in Biology, Chemistry, Biochemistry, Engineering, or a related scientific discipline.
• 4-6 years of experience in Quality Assurance, Quality Operations, or Manufacturing within pharmaceutical, biotechnology, or…