Job Title: Technical WriterJob Description
The Technical Writer leads and authors thorough investigations of deviations within pharmaceutical manufacturing processes, including formulation, filling, and packaging. This role ensures compliance with cGMP regulations by identifying root causes, driving effective corrective and preventive actions (CAPAs), and supporting continuous improvement initiatives across the organization. The position offers the opportunity to work in a growing company with multiple new products and an exciting pipeline.
Responsibilities

+ Lead end-to-end deviation investigations involving manufacturing operations such as aseptic and sterile filling, formulation and compounding, and packaging and inspection.

+ Identify, document, and classify deviations from standard operating procedures (SOPs), batch records, and regulatory requirements.

+ Perform structured root cause analysis (RCA) using tools such as 5 Whys and Fishbone (Ishikawa...