Medasource
Deviation Investigation Associate (Concord)
Medasource, Concord, North Carolina, United States, 28027
Job Title:
Deviation Investigation Writer/Associate Location:
Concord, NC Type:
6-Month Contract (Potential for Extension or Conversion) Schedule:
MondayFriday, 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 deviationsunexpected 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.
Deviation Investigation Writer/Associate Location:
Concord, NC Type:
6-Month Contract (Potential for Extension or Conversion) Schedule:
MondayFriday, 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 deviationsunexpected 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.