QC Lab Team Supervisor (Pharmaceutical Manufacturing)

Location: Swiftwater, Pennsylvania, United States; laboratory-based role with standard working hours and possible overtime.

Salary: $90,000–$130,000 per year

Company

hirify.global is an R&D-driven biopharmaceutical company developing medicines and vaccines through science, digital capabilities, and AI-enabled innovation.

What you will do

• Oversee daily quality control laboratory operations, sample testing, scheduling, shopfloor reviews, and testing coverage.
• Maintain GMP compliance, validated methods, laboratory quality systems, and regulatory readiness.
• Investigate quality events, deviations, product complaints, discrepancies, CAPAs, and audit findings.
• Author and review procedures, protocols, technical reports, memorandums, change controls, and quality documents.
• Lead, train, qualify, and mentor laboratory staff while supporting hiring and continuous improvement.
• Maintain laboratory equipment, facilities, calibration, qualification, and specialized analytical activities including Micro-FTIR, SEM/EDS, CCIT, and BLGF testing.

Requirements

• Bachelor’s degree in life sciences, pharmaceutical sciences, engineering, or a related scientific field and at least 8 years of experience in a cGMP environment.
• Progressive quality control experience in pharmaceutical or vaccine manufacturing, from laboratory technician through laboratory management responsibilities.
• Comprehensive knowledge of GMP and FDA, EMA, and ICH regulatory requirements.
• Hands-on experience with particulate isolation, Micro-FTIR, and SEM/EDS analysis in a regulated pharmaceutical environment.
• Experience with technical documentation, audits and inspections, method validation and transfer, laboratory instrumentation, and LIMS and quality systems.
• Must be eligible under the stated US/Puerto Rico resident hiring scope and able to work in a laboratory environment with chemicals, specialized equipment, and PPE.

Nice to have

• Experience with USP, EP, or JP compendial standards.
• Lean and continuous improvement experience, including cost and efficiency metrics.
• HSE representative experience, GEMBA walks, Satellite Accumulation Area inspections, and laboratory safety initiatives.

Culture & Benefits

• Supportive, future-focused environment centered on medicines, vaccines, and scientific innovation.
• Career growth opportunities through promotions and international or lateral moves.
• Healthcare, prevention, wellness, and broader employee benefits.
• At least 14 weeks of gender-neutral parental leave.
• Use of digital, data, and AI-driven technologies in manufacturing and supply operations.