GMP QA Documentation Specialist

Natureplex,-LLC; Olive Branch (MS); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Paid Vacation

Medical Insurance with 80% coverage

Dental and vision insurance

Short-term Disability

Voluntary Life Insurance

Company-paid life insurance

401(k) plan with company-matching

Weekly pay

ZayZoon - wage access

Job summary

Natureplex is seeking a Quality Assurance Technical Writer to join our Olive Branch, MS team. You will develop, review, and maintain GMP-focused documentation to support QA operations and regulatory compliance.

Strong technical writing, attention to detail, and clear communication of complex information are essential. Responsibilities include SOPs, deviation/change controls, audits support, and cross-department collaboration.

Qualifications

• Experience preparing, reviewing, or maintaining technical documentation in a regulated environment.
• Strong technical writing, editing, proofreading, and organizational skills.
• Proficiency in Microsoft Word and Excel.
• Ability to interpret technical information and communicate it clearly and accurately.
• Experience with GMP documentation and ALCOA data integrity principles.

Responsibilities

• Develop, write, edit, and maintain SOPs, work instructions, and GMP documentation.
• Review documentation for accuracy, clarity, and regulatory compliance (FDA).
• Maintain controlled documents including revisions, approvals, version control, and archiving.
• Prepare and revise deviation reports, change controls, testing protocols, and other quality documents.
• Support internal and regulatory audits by organizing required documentation.
• Provide documentation-related training and support as needed.

Skills

Technical writing

Editing

Proofreading

Organizational skills

Education

Associate's or bachelor's degree in English/Technical Writing/Science

Tools

Microsoft Word

Microsoft Excel

Job description

Natureplex is seeking a Quality Assurance Technical Writer to join our Olive Branch, MS team. You will develop, review, and maintain GMP-focused documentation to support QA operations and regulatory compliance.

Strong technical writing, attention to detail, and clear communication of complex information are essential. Responsibilities include SOPs, deviation/change controls, audits support, and cross-department collaboration.