Job Title : Deviation Investigation Writer / Associate
Location : Concord, NC
Type : 6-Month Contract (Potential for Extension or Conversion)
Schedule : Monday–Friday, 8 : 00 AM – 5 : 00 PM
Overview :
We are seeking two detail-oriented and driven professionals to join a dynamic manufacturing
operations team as Deviation Investigation Writers. These individuals will play a critical role in
supporting quality compliance by documenting and investigating deviations—unexpected events that
impact product quality, safety, or regulatory standards.
Key Responsibilities :
- Ghostwrite deviation investigation reports on behalf of technical staff, including operators and
engineers.
Collaborate with subject matter experts to gather information and draft clear, audit-readydocumentation.
Support root cause investigations (RCI) and contribute to continuous improvement efforts.Assist in managing deviations across various manufacturing areas, including filling, inspectionrobotics, and process operations.
Ensure documentation meets regulatory standards and is easily understandable by auditors andcross-functional teams.
Required Qualifications :
Proven experience in technical writing , preferably in a regulated or manufacturingenvironment.
Background in quality assurance , engineering , or a related technical field.Ability to quickly learn complex manufacturing processes and translate them into clear,structured documentation.
Strong analytical and communication skills.Comfortable working independently and collaboratively in a fast-paced setting.Preferred Qualifications :
Experience writing deviation investigation reports or supporting root cause analysis .Familiarity with manufacturing environments such as pharmaceutical , chemical , or foodproduction .
Understanding of parenteral manufacturing processes is a plus, but not required.