Quality Control Technical Writer – GMP Validation

SGS Consulting; Milton (MA); On-site; USD 70,000 - 110,000; Full time

Job summary

SGS Consulting is seeking a QC support professional to assist the Product Technical Support team in validation document generation for client site product validation. Strong microbiology knowledge and GMP writing experience are required.

The role emphasizes collaboration with SMEs, data review, and generating GMP documentation while coordinating timelines across sites. A science degree in microbiology or related field is preferred.

Qualifications

• Experience writing GMP documentation in biopharmaceutical settings is preferred.
• Familiarity with validation concepts and data review processes.
• Strong documentation, organization, and attention to detail.

Responsibilities

• Author method validation documents using document workflow with SMEs.
• Coordinate validation document generation to support product validation at client site.
• Facilitate lifecycle management through collaboration with SMEs and analysts.
• Participate in across-site meetings and track project timelines.

Skills

QC microbial support

Technical writing

Interpersonal skills

Written communication

Microbiology

Education

Science degree in microbiology or related field

Tools

LIMS

Job description

SGS Consulting is seeking a QC support professional to assist the Product Technical Support team in validation document generation for client site product validation. Strong microbiology knowledge and GMP writing experience are required.

The role emphasizes collaboration with SMEs, data review, and generating GMP documentation while coordinating timelines across sites. A science degree in microbiology or related field is preferred.