Logistics & QC Analyst – Inbound Ops & Compliance

Boehringer Ingelheim GmbH; Fremont (CA); On-site; USD 75,000 - 112,000; Full time

Job summary

Boehringer Ingelheim is seeking a Logistics Analyst to provide QC and inbound operations oversight in a multi-product biopharmaceutical setting. You will monitor KPIs, support compliance, coordinate shipments and contribute to continuous improvement.

The role requires degrees in science or engineering, GMP experience, ability to work with audits, and cross-functional collaboration. Standard hours Monday–Friday, 7:30am–4:30pm PST, and competitive compensation and benefits.

Qualifications

• Bachelor's or Master’s in science or engineering required; Master’s preferred.
• 4+ years in analytical testing in a GMP environment.
• Subject matter expert in analytical methods and data interpretation.
• Experience with SOPs, regulatory guidelines and quality systems.
• Strong communication and collaboration skills.

Responsibilities

• Manage sample shipments via Boehringer Ingelheim approved freight carriers (small parcel, LTL, FTL).
• Coordinate inbound logistics and verify documentation and materials.
• Document work according to cGMP and SOPs; follow site regulations.
• Report abnormalities, deviations and safety concerns promptly.
• Lead trainings, participate in audits and support corrective actions.
• Coordinate and review analytical testing of bulk drug substance and product.
• Assist in equipment qualifications and maintenance tasks.
• Collaborate cross-functionally with Trade Compliance and other teams.

Skills

GMP Compliance

Analytical testing

Documentation

Regulatory audits

Cross-functional

Quality systems

Attention to detail

Problem solving

Education

Bachelor's degree in science or engineering

Master's degree preferred

Job description

Boehringer Ingelheim is seeking a Logistics Analyst to provide QC and inbound operations oversight in a multi-product biopharmaceutical setting. You will monitor KPIs, support compliance, coordinate shipments and contribute to continuous improvement.

The role requires degrees in science or engineering, GMP experience, ability to work with audits, and cross-functional collaboration. Standard hours Monday–Friday, 7:30am–4:30pm PST, and competitive compensation and benefits.