2nd-Shift Manufacturing Investigations Lead

JMD Technologies Inc.; Boston (MA); On-site; USD 69,000 - 90,000; Full time

Job summary

JMD Technologies Inc. in Boston, MA is seeking a Manufacturing Investigations Staff for the 2nd shift on a 12+ month contract. The role focuses on leading quality records and investigations to support pharmaceuticals manufacturing.

You will manage deviations, CAPAs, Change Controls, and related GMP investigations, perform root cause analysis, and drive corrective actions from initiation to closure.

Qualifications

• Experience in quality events management, deviations, CAPAs, Change Controls, and investigations.
• Experience performing root cause analysis and implementing corrective actions.
• Experience in pharmaceutical/biopharmaceutical GMP manufacturing.

Responsibilities

• Lead and execute Deviations, CAPAs, Change Controls, and QC/Analytical Investigations.
• Lead deviation triage, investigation planning, event initiation, and impact assessments.
• Investigate across Manufacturing, QC, Materials, Facilities, and Equipment operations.
• Conduct SME interviews, GEMBA, data review, and root cause analysis.
• Lead and document root cause investigations and recommend corrective actions.
• Own CAPAs and Change Controls from initiation to closure.

Skills

5+ years experience

Quality event management

Root cause analysis

GMP / regulatory

CAPA / Change Control

Job description

JMD Technologies Inc. in Boston, MA is seeking a Manufacturing Investigations Staff for the 2nd shift on a 12+ month contract. The role focuses on leading quality records and investigations to support pharmaceuticals manufacturing.

You will manage deviations, CAPAs, Change Controls, and related GMP investigations, perform root cause analysis, and drive corrective actions from initiation to closure.