Medasource
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 other subject matter experts. 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. Seniority level
Not Applicable Employment type
Full-time Job function
Manufacturing and Quality Assurance Industries: Pharmaceutical Manufacturing Get notified about new Investigations Specialist jobs in Concord, NC.
#J-18808-Ljbffr
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 other subject matter experts. 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. Seniority level
Not Applicable Employment type
Full-time Job function
Manufacturing and Quality Assurance Industries: Pharmaceutical Manufacturing Get notified about new Investigations Specialist jobs in Concord, NC.
#J-18808-Ljbffr