52 Siegfried Engineering Jobs Hiring Near You

• 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.

• Serve as the primary QA leader supporting second-shift sterile and aseptic manufacturing operations.
• 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 other GMP-regulated environments.
• Demonstrated supervisory, team lead, or people leadership experience.
• Strong understanding of cGMP requirements, FDA regulations, and quality systems.
• Excellent communication, coaching, problem-solving, and decision-making skills.
• Proven ability to make sound, risk-based quality decisions in a fast-paced manufacturing environment.

• Experience supporting sterile and aseptic manufacturing operations.
• Experience working in a pharmaceutical CDMO environment.
• Knowledge of EU GMP and Annex 1 requirements.
• Experience working within Grade A-D cleanroom environments.
• Familiarity with TrackWise, SAP, LIMS, or other electronic quality systems.
• Experience supporting client audits, customer visits, and regulatory inspections.

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.