Writer: Quality Compliance Position Available In Northampton, Pennsylvania

FREELANCE OPPORTUNITY

Quality Compliance Writer Target Start Date:

Mid July Location:

Fully Remote Length:

Through End of Year (with potential extension)

Interview Process:

1-2 rounds

About:

Our client is a recognized leader in healthcare solutions, including nutrition, pharmacy admixture, and dialysis. As part of a global group the company is committed to safety, innovation, and knowledge sharing to help eliminate treatment errors and reduce costs. To accomplish this, they make sure all their SOPs, and quality agreements are properly communicated in written form.

Department Details:

Reports to:

Quality Assurance Team:

Distributed across multiple U.S. locations

Environment:

Collaborative, compliance-focused, with structured documentation and processes

Ideal Candidate Experience:

Industry Background:

Pharmaceutical or Medical Device Role Fit:

Quality Generalist or Quality Analyst with documentation experience in a regulatory environment

Key Strengths:

Writing, document control, and SOP development within FDA-regulated industries

Key Responsibilities:

Write, revise, and maintain Quality Agreements (20-30 pages, template-based with provided data) Draft and update SOPs and Work Instructions Support Quality Compliance documentation: clearly defining roles/responsibilities between client and suppliers Investigate and document quality issues, helping implement preventive actions

Writing Expectation:

Approximately 25-30% of documentation will require net-new (original) content creation Remaining work involves adapting or updating existing templates with project-specific data No AI writing tools permitted in the creation of official documentation

Experience:

Bachelor Degree 2-4 years experience in similar role Regulated, medical devises/pharm experience, preferred

DIGITAL PEOPLE IS PROUD TO OFFER OPTIONAL MAJOR MEDICAL, DENTAL, VISION AND 401K BENEFITS.

#LI-SS2 #

LI-REMOTE

Job Number:

1915491