GMP Validation & QA Consultant - Onsite Boston

JMD Technologies Inc.; Boston (MA); On-site; USD 82,656 - 89,544; Part time

Job summary

A leading life sciences consulting firm is seeking a Validation & Quality Assurance Consultant to provide QA support for GMP operations in Boston. This role includes hands-on experience with validation activities, root cause analysis, and collaboration with cross-functional teams. The ideal candidate has a Master's degree with relevant experience or a Bachelor's degree and extensive background in engineering or sciences. Salary is competitive, with an hourly estimate of $60-$65 depending on experience.

Qualifications

• Experience providing QA support for GMP operations.
• Hands-on experience with aseptic processing.
• Strong experience in investigations and CAPA management.
• Familiarity with systems such as Veeva, Nuvolo, and Viewlinc.

Responsibilities

• Provide QA oversight for GMP manufacturing.
• Support validation activities and document reviews.
• Lead event investigations and CAPA implementation.
• Ensure compliance with GMP standards across functions.

Skills

QA oversight

Aseptic processing

Investigations

Root Cause Analysis

CAPA management

Quality systems

Education

Master's degree with 3-5 years experience

Bachelor's degree in engineering, scientific, or related field with 8+ years experience

Tools

Veeva

Nuvolo

Viewlinc

Job description

A leading life sciences consulting firm is seeking a Validation & Quality Assurance Consultant to provide QA support for GMP operations in Boston. This role includes hands-on experience with validation activities, root cause analysis, and collaboration with cross-functional teams. The ideal candidate has a Master's degree with relevant experience or a Bachelor's degree and extensive background in engineering or sciences. Salary is competitive, with an hourly estimate of $60-$65 depending on experience.