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-ready
documentation.
• Support root cause investigations (RCI) and contribute to continuous improvement efforts.
• Assist in managing deviations across various manufacturing areas, including filling, inspection
robotics, and process operations.
• Ensure documentation meets regulatory standards and is easily understandable by auditors and
cross-functional teams.
Required Qualifications:
• Proven experience in technical writing , preferably in a regulated or manufacturing
environment.
• 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 food
production .
• Understanding of parenteral manufacturing processes is a plus, but not required.
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