Quality Control Manager

Piper Companies is seeking a Quality Control Manager to join a reputable Biologics Quality Control Testing company located in Wayne, Pa.  

Responsibilities of the Quality Control Manager include:  

• Lead projects, collaborate with clients and teams, and ensure expectations are met 
•  Oversee testing, manage deviations, and ensure adherence to global regulations 
• Represent the team in audits, address issues, and implement corrective actions 
• Manage assay development, validation, and ongoing compliance 
• Maintain documentation, refine processes, and drive quality initiatives 
• Train, mentor, and manage staff while overseeing lab assignments 
• Ensure compliance with local, state, and federal regulations 
• Monitor business metrics, report progress, and resolve issues 

Qualifications for the Quality Control Manager include:  

• 6+ years of GMP lab experience in pharmaceuticals, medical devices, or biotechnology. 
• Knowledge of molecular biology and sequencing-based applications. 
• Essential supervisory or management experience. 
• SME in NGS, CSV, validation, quality, GMP, SOPs, lab operations, and QMS (Trackwise). 
• PhD in a scientific or technical discipline (e.g., biological science) with 3+ years of relevant experience. 
• MA/MS in a scientific or technical discipline with 6+ years of relevant experience. 

Compensation for the Quality Control Manager include:  

• Salary Range: $100-120k **Depending on experience**  
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays  

This job opens for applications on 3/21/2025. Applications for this job will be accepted for at least 30 days from the posting date.  

Keywords: SME, NGS, CSV, GMP, SOP, CAPA, Trackwise, biological science, technical discipline, business metrics, compliance, assay documentation, audits, collaborate, Quality Control, Biologics, Quality Assurance, GMP (Good Manufacturing Practices), Regulatory Compliance, Quality Management Systems (QMS), Risk Management, Process Improvement, Analytical Testing, Laboratory Management, Standard Operating Procedures (SOPs), Inspection and Testing, Data Analysis, Root Cause Analysis, Corrective and Preventive Actions (CAPA), Quality Audits, Documentation, Team Leadership, Continuous Improvement, Product Release, Validation and Verification, Biopharmaceuticals, Compliance Monitoring, Quality Metrics, Customer Satisfaction 

#LI-KT1 #LI-ONSITE