Quality Supervisor

Langham Logistics; Easton (Northampton County); On-site; USD 80,000 - 110,000; Full time

Job summary

Langham Logistics seeks a Quality Supervisor to lead the Raw Material Warehouse and Sampling Suite, ensuring strict cGMP compliance and rigorous documentation. This on-site leadership role balances hands-on validation with quality systems governance.

You will manage floor staffing, oversee environmental monitoring, instrument-based inspections, CAPA and deviations, and serve as the primary contact for client and regulatory audits.

Qualifications

• Bachelor’s degree in a scientific or technical discipline or equivalent professional experience.
• Minimum 3 years of hands-on Quality experience in a cGMP-regulated environment (pharma/biotech/medical devices).
• Previous supervisory or managerial experience is required with ability to coach and manage headcount and schedules.
• Deep understanding of cGMP, GDP, and GDocs as they apply to raw materials handling and regulatory frameworks.
• Proficient in MS Office and ability to review complex quality data and implement compliant solutions.

Responsibilities

• Plan daily floor manpower and allocate tasks based on priorities.
• Govern the cGMP Sampling Environment with strict cleanroom oversight and contamination control.
• Execute material quality control by inspecting incoming raw material lots and using analytical tools to verify specs.
• Drive quality systems including deviations, CAPA, and change controls; cross-train staff for data retention and integrity.
• Host external and regulatory audits as primary quality contact and ensure audit defensibility.

Skills

Leadership

Analytical thinking

Problem solving

Collaboration

Education

Bachelor’s degree in science/technical field

Tools

LIMS

Raman spectroscopy

Calipers

Gauges

Job description

Are you Rady to Shape the Future of Logistics Quality?

We are seeking a Quality Supervisor to serve as the critical gatekeeper for our Raw Material Warehouse and Sampling Suite. This isn't a passive oversight role; it is a dynamic floor leadership position designed for an analytical, proactive supervisor who commands a strong understanding of cGMP cleanroom protocols and documentation integrity. If you are ready to lead a high-performing team of Quality Associates, interface directly with global pharma clients, and maintain a constant state of audit readiness, we want you on our frontline.

Key Expectations

The Quality Supervisor will directly manage the daily compliance, environment, and personnel footprint inside our specialized raw materials sampling suite. This position will balance hands-on material validation with rigorous quality systems governance.

Plan & Allocate Floor Manpower: Daily Operations.

Design daily schedules and balance workloads based on shifting operational and client priorities. Assign frontline associates to specialized suite functions including cleanroom gowning, material checks, and environmental monitoring based on their technical skills.

Govern the cGMP Sampling Environment: Cleanroom Oversight.

Maintain absolute control over the Raw Material Sample Suite. Oversee precise cleanroom workflows, trafficking patterns, rigorous cleaning schedules, and contamination control procedures to safeguard product integrity.

Execute Material Quality Control: Gatekeeping & Tools.

Physically inspect incoming raw material lots for hidden damage or discrepancies. Empower your team to confidently accept or reject batches using specialized inventory systems and analytical tools (such as LIMS, Raman spectroscopy, calipers, and gauges) to verify client specifications.

Drive Quality Systems & Sourcing: CAPA & Deviations.

Own, document, and advance critical quality system processes including deviations, change controls, and thorough root-cause investigations. Cross-train floor associates to ensure high-accuracy document retention and data integrity.

Host External & Regulatory Audits: Audit Defensibility.

Serve as the primary quality contact and technical anchor for internal reviews, major client inspections, and strict regulatory audits (including FDA, DHS, and OSHA). Ensure all quality records are maintained in an organized, instantly retrievable layout.

Requirements & Core Qualifications

We look for straight-forward leaders who pair strong technical analytical skills with an exceptional work ethic and a collaborative approach to problem-solving.

• Education: Bachelor’s degree in a scientific or technical discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences) or equivalent professional industry experience.
• Experience: Minimum 3 years of hands-on Quality experience in a strict, cGMP-regulated environment (Pharma, Biotech, or Medical Devices).
• Leadership: Previous supervisory or managerial experience is required. Proven ability to coach, cross-train, and manage headcount, schedules, and absenteeism.
• Regulatory Knowledge: Deep understanding of current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP), and Good Documentation Practices (GDocs) as they apply to raw materials handling, FDA, and Department of Homeland Security (DHS) frameworks.
• Systems & Analytics: Computer literate (Microsoft Office Suite) with the analytical capacity to review complex quality data records, evaluate operational risks, and implement compliant solutions quickly.

Physical Demands & Work Environment: Physical movements include bending, stooping, and lifting to 50 pounds as part of daily work routine. Will work on concrete in a warehouse environment (subject to heat and cold). Work is performed in a warehouse environment subject to temperature variances.

Disclaimer: This job description is not intended to be all-inclusive. This position may be required to perform other related duties assigned to meet the ongoing needs of the organization. Langham reserves the right to modify job responsibilities and expectations as business demands evolve.