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Quality Assurance Technical Writer
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Based on New Jersey data
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What they do
A Technical Writer writes product instructions, user manuals or other material that helps to explain complex information or procedures. Writes help information available to customers online, or clear explanations of company policies. Supports internal communication among different technical, engineering and scientific specialists working on a project or product. Creates product documentation, and provides input for improving product design.
$72,746 / year median in New Jersey
-11% projected decline
Job Description
- Review and act as author/technical writer to alterations to Master Batch record and QA documentation
- Correct and revise documentation as needed
- Advise manufacturing personnel on proper documentation
- Utilize knowledge of FDA and GMP regulations to ensure compliance Qualifications for the Quality Assurance Technical Writer include:
- A minimum of 1-5 years' experience within Pharmaceutical Manufacturing (sterile injectable is preferred)
- Hands on experience with QA documentation
- Proficiency in Microsoft Office
- B.S. in business or scientific field preferred Compensation for the Quality Assurance Technical Writer include:
- Salary Range is dependent upon experience.
- Comprehensive benefits package Keywords Quality Assurance Technical Writer, QA, Pharmaceutical, Branchburg, NJ, New Jersey, FDA, GMP, Batch Record, Manufacturing, GDP, cGMP, Clinical Manufacturing, Regulatory Review, #