GMP Technical Writer — QMS & Compliance Lead

Experic LLC; Cranbury Township (NJ); On-site; USD 80,000 - 110,000; Full time

Job summary

Experic LLC is seeking a Technical Writer based in Cranbury Township, NJ. This role involves drafting and maintaining GMP documentation in collaboration with Operations and Quality Assurance teams. Candidates should have a Bachelor’s degree and over 3 years of relevant experience in a regulated GMP environment.

The position offers a salary range of $80,000 to $110,000, primarily in an office setting. Strong technical writing abilities and meticulous attention to detail are essential.

Qualifications

• 3+ years of experience in a GMP environment.
• Experience leading Root Cause Analysis.
• Familiarity with cGMP requirements and FDA regulatory expectations.

Responsibilities

• Lead deviation and complaint Root Cause Analysis and CAPA.
• Draft, revise, and format GMP documentation.
• Ensure documents are compliant and inspection ready.

Skills

Technical writing

Attention to detail

Organizational skills

Collaboration

GMP knowledge

Document management

Education

Bachelor’s degree in Life Sciences, Engineering, Technical Writing or related field

Tools

Microsoft Office

Electronic document management systems

Job description

Experic LLC is seeking a Technical Writer based in Cranbury Township, NJ. This role involves drafting and maintaining GMP documentation in collaboration with Operations and Quality Assurance teams. Candidates should have a Bachelor’s degree and over 3 years of relevant experience in a regulated GMP environment.

The position offers a salary range of $80,000 to $110,000, primarily in an office setting. Strong technical writing abilities and meticulous attention to detail are essential.