Associate Technical Writing

Summary

Develops, writes, edits, and formats materials such as Standard Operating Procedures, forms, methods and related technical and business process documentation for the Quality Control organization. When creating, updating and enhancing the documentation, adhere to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality. Additionally, this position will be required to administer the processing of documents in the controlled document system.

Responsibilities

Assist with writing laboratory documentation (standard operating procedures, guidance documents, forms, etc) for the QC Laboratory group.Manage the review/approval process in the controlled document system.Assist other lab staff with formatting/editing of documents.Update/help manage master document tracker for new lab startup project.

Skills

MS Office expertiseTechnical writing experienceExcellent communication/writing skillsKnowledge of Good Documentation Practices preferredGeneral laboratory/quality control knowledge preferred

Top 3 Must Have Skill Sets

Technical writing experience required.Strong attention to detail and the ability to self manage work/projects1+ year of previous pharma experience with a understanding of the GMP process.

Compensation

The pay rate range above is the base hourly pay range that Aditi Consulting reasonably expects to pay someone for this position (compensation may vary outside of this range depending on several factors, including but not limited to, a candidate’s qualifications, skills, competencies, competencies, experience, location and end client requirements).

Benefits and Ancillaries

Medical, dental, vision, PTO benefits and ancillaries may be available for eligible Aditi Consulting employees and vary based on the plan options selected by the employee.