Natureplex is a dynamic, privately held pharmaceutical manufacturer dedicated to revolutionizing over-the-counter medicines and electrolytes. Founded in 2001, we proudly offer proprietary brands, private label products, and contract packaging services. With two locations in Memphis, Tennessee, and Olive Branch, Mississippi, we are on an exciting path of rapid expansion, creating strong career advancement and personal growth opportunities.

We invite you to apply for the Quality Assurance Technical Writer role at our Olive Branch, MS location, where you will become a vital part of our dynamic team. This position develops, reviews, revises, and maintains technical documentation to support Good Manufacturing Practices (GMP), regulatory compliance, and quality assurance operations. The ideal candidate will possess strong technical writing skills, excellent attention to detail, and the ability to communicate complex technical information clearly and accurately.

In addition to career growth, we also offer a range of benefits and perks to our employees

These include:

- Paid Vacation

- Medical Insurance with 80% coverage for employees and 20% for dependents

- Dental and vision insurance

- Short-term Disability

- Voluntary Life Insurance

- Company-paid life insurance

- 401(k) plan with company-matching

- Weekly pay

- ZayZoon - gives you instant access to your wages ahead of payday

We provide equal employment opportunities and create a safe and fair work environment for all employees.

Natureplex participates in E-Verify.

Key Responsibilities

• Develop, write, edit, and maintain Standard Operating Procedures (SOPs), work instructions, technical reports, and GMP documentation.
• Review documentation for accuracy, clarity, consistency, and compliance with applicable FDA regulations.
• Maintain controlled documents, including revisions, approvals, version control, and document archiving.
• Prepare and revise deviation reports, change controls, testing protocols, and other quality-related documentation.
• Ensure documentation meets GMP requirements and ALCOA data integrity principles.
• Collaborate with Quality Assurance, Quality Control, Manufacturing, and other departments to gather and verify technical information.
• Support internal and regulatory audits by preparing, reviewing, and organizing required documentation.
• Assist in reviewing analytical procedures, testing documentation, and technical reports.
• Provide documentation-related training and support as needed.
• Perform other duties as assigned.

Required Qualifications

• High school diploma or equivalent.
• Experience preparing, reviewing, or maintaining technical documentation in a regulated environment.
• Strong technical writing, editing, proofreading, and organizational skills.
• Proficiency in Microsoft Office, particularly Word and Excel.
• Ability to interpret technical information and communicate it clearly and accurately.
• Strong attention to detail and ability to manage multiple assignments and deadlines.

Preferred Qualifications

• Associate's or bachelor's degree in English, Technical Writing, Chemistry, Biology, or a related field.
• Experience in pharmaceutical manufacturing, Quality Assurance, Quality Control, or a related FDA-regulated industry.
• Knowledge of current Good Manufacturing Practices (cGMP), FDA regulations, and document control procedures.
• Experience with SOPs, deviation investigations, change controls, and audit documentation.
• Familiarity with ALCOA data integrity principles.
• Bilingual English/Spanish skills, including technical document translation.

• Monday through Friday
• Minimum 40 hours per week
• Additional hours may be required based on business needs.