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Deviation Investigator Jobs (NOW HIRING)

TriOptus LLC

Deviation Investigator

Princeton, NJ ยท On-site

Manage deviation records and monitor completion of corrective actions within a Quality Management System. * Investigate IT incidents with technical and business stakeholders to define if there is ...

TekWissen LLC

Quality Records Investigator

Houston, TX ยท On-site

$20 - $24/hr

Quality Records Investigator / Deviation Investigator/Initiator Location: Houston, TX, 77047 Duration: 6 Months - Possibility to Extend Job Type: Temporary Assignment Work Type: Onsite Shifts: Monday ...

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$32K

$75.3K

$131K

How much do deviation investigator jobs pay per year?

As of Jun 9, 2026, the average yearly pay for deviation investigator in the United States is $75,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What does a typical workday look like for a Deviation Investigator?

A typical day for a Deviation Investigator involves reviewing deviation reports, gathering data from production or laboratory records, and conducting interviews with staff to determine the root cause of incidents. You will document findings in compliance with standard operating procedures and collaborate closely with cross-functional teams, such as manufacturing, quality assurance, and regulatory affairs, to recommend corrective and preventive actions. Many Deviation Investigators participate in regular meetings to discuss ongoing cases and share best practices. The role requires excellent organizational skills to manage multiple investigations concurrently while ensuring timely and thorough resolution.

What is a Deviation Investigator job?

A Deviation Investigator is responsible for analyzing deviations in manufacturing, quality control, or laboratory processes within industries like pharmaceuticals or biotechnology. They identify root causes, document findings, and implement corrective and preventive actions (CAPAs) to ensure compliance with regulatory standards. Their role is crucial in maintaining product quality, safety, and adherence to Good Manufacturing Practices (GMP). Effective communication, problem-solving skills, and knowledge of industry regulations are essential for this position.

What are the key skills and qualifications needed to thrive in the Deviation Investigator position, and why are they important?

To thrive as a Deviation Investigator, you need a strong background in quality assurance or compliance, along with experience in root cause analysis and deviation management, often supported by a degree in a scientific or technical field. Familiarity with industry regulations (such as GMP or ISO standards), quality management systems (QMS), and tools like TrackWise or MasterControl is highly desirable. Strong analytical thinking, attention to detail, effective communication, and the ability to work collaboratively are key soft skills for this role. These skills ensure accurate investigation, thorough documentation, and prompt resolution of deviations to maintain product quality and regulatory compliance.

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What cities are hiring for Deviation Investigator jobs? Cities with the most Deviation Investigator job openings:
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Deviation Investigator jobs near you
Infographic showing various Deviation Investigator job openings in the United States as of June 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $75,325 per year, or $36.2 per hour.
Deviation Investigator

Deviation Investigator

TriOptus LLC

Princeton, NJ โ€ข On-site

Other

This job post hasย expired today.ย Applications are no longer accepted.

Job description

Job Description:
  • This role will be responsible for the investigation of IT Enterprise related deviations to determine root cause and applicable corrective and preventive actions in accordance with FDA, MHRA, and other applicable global health authority regulations.
  • Collaborate with IT and Quality resources to collect relevant information for deviation assessment and facilitate meetings with investigation teams.
  • Manage deviation records and monitor completion of corrective actions within a Quality Management System.
  • Investigate IT incidents with technical and business stakeholders to define if there is potential GxP impact and requirement to raise a quality deviation and subsequent investigation.

Required Competencies:
Knowledge, Skills, and Abilities:
  • Thorough knowledge of and competence in IT processes, including but not limited to deviations, investigations, CAPA management, SLC, computer system validation, and change management.
  • Must have strong knowledge and experience with cGMP, GCP, GLP Quality, and Compliance.
  • Must have strong authorship and be able to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles.
  • Must be able to note technical attributes in potential situations or issues and process IT-based solutions across most of the job function.
  • Must be able to effectively prepare communications with interpretation of data analysis and potential problems to management and the group with clarity and a high level of accuracy.
  • Must provide guidance to other employees in the interpretation of technical issues across an interdisciplinary teams.
  • Must be action-oriented and customer-focused, building relationships, problem solving, planning and organizing, conflict management, resource allocation, coaching other and analytical thinking.
  • Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision.
  • Work is self-directed.
  • Confident in making decisions for minor issues.
  • Routinely recognizes Quality issues and solves problems.
  • Proposes solutions for complex issues and works with management to resolve.
  • Follows established procedures and performs work as assigned.
  • Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution.
  • Ability to interpret results and situations and articulate recommendations for resolution.
  • Able to write and review reports with clarity and brevity.
  • Teamwork and ability to work effectively across functional groups and teams to ensure requirements are met.
  • Excellent verbal and written communication skills.
  • Advanced knowledge of complete MS Office suite.
  • Firm understanding of technology platforms as needed for project.
  • Experience with electronic document management systems (e.g. documentum, Qumas, SharePoint etc.); application development and lifecycle management; and IT service management systems (e.g. ServiceNow, SAP Solution Manager, etc)
  • Excellent oral and written communication skills in English.

Education and Experience:
  • B.S. degree required; advanced degree preferred.
  • Minimum 5 years Quality Assurance and/or IT experience in a pharmaceutical company

Skills:
  • CAPA: 3 to 5 years
  • CSV: 6 to 10 years
  • Deviations: 6 to 10 years
  • FDA Regulations: 6 to 10 years
  • Investigations: 6 to 10 years

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