GMP QA Manager, Life Science Materials

Langham Logistics, Inc; Town of Easton (WI); On-site; USD 90,000 - 120,000; Full time

Job summary

Langham Logistics, Inc. is seeking an Associate Quality Manager for the Life Science Division in Easton.

You will lead a team responsible for GMP-compliant sampling, testing, and material quality control in our Pharmaceutical Raw Material Warehouse and Sampling Suite. The role focuses on maintaining regulatory compliance with FDA/EU/ICH guidelines, managing quality records, and coordinating with QA, Warehouse, and Operations for timely issue resolution.

Qualifications

• Bachelor’s degree in scientific or technical discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences) or equivalent experience.
• Minimum 3 years of Quality experience in pharmaceutical manufacturing or distribution environment.
• Strong knowledge of GMP regulations (FDA, EU, ICH).
• Previous Supervisory or Managerial experience required.

Responsibilities

• Lead, mentor, and develop a team of Quality Associates in the Pharmaceutical Raw Material Sample Suite, promoting compliance and continuous improvement.
• Ensure sampling, inspection, and testing activities conform to GMP, FDA, and client requirements while overseeing cleanroom operations.
• Manage quality system processes including deviations, CAPA, change control, investigations, and training for the Sample Suite.
• Oversee quality checks for incoming raw materials and sampling processes, ensuring product integrity and traceability.
• Serve as primary quality contact for audits and client inquiries, ensuring timely, compliant communication.
• Identify process gaps and lead initiatives to improve efficiency and regulatory compliance, with risk assessments.

Skills

GMP knowledge

Regulatory compliance

Quality management

Leadership

Communication

Education

Bachelor's degree in a scientific or technical discipline

Job description

Langham Logistics, Inc. is seeking an Associate Quality Manager for the Life Science Division in Easton.

You will lead a team responsible for GMP-compliant sampling, testing, and material quality control in our Pharmaceutical Raw Material Warehouse and Sampling Suite. The role focuses on maintaining regulatory compliance with FDA/EU/ICH guidelines, managing quality records, and coordinating with QA, Warehouse, and Operations for timely issue resolution.