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Full Time Deviation Investigator Jobs (NOW HIRING)

Pomona, CA (In-office) Position Type: Full-time, Vacancy Status:This position is vacant AI ... Lead deviation investigations, OOS events, and non-conformances, including root cause analysis and ...

Pomona, CA (In-office) Position Type: Full-time, Vacancy Status: This position is vacant AI ... review, deviation investigations, CAPA oversight, and audit readiness. The Lead acts as a key ...

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

Support deviation investigations, change control activities, and CAPAs. * Participate in method ... Comfortable working on-site full-time; no remote options. Preferred Experience: * Hands-on ...

Stable, full-time opportunity with a predictable schedule * Strong benefits package * Hands-on role ... Support deviation investigations by assisting with inspections, swabbing, sample pulls, and ...

Support deviation investigations, CAPAs, and root cause analysis for automation-related issues ... Quality Agents offers a full suite of benefits for full-time employees including: Health, dental ...

... deviation investigations, CAPAs, and root cause analysis for automation-related issues Minimum ... Quality Agents offers a full suite of benefits for full-time employees including: • Health ...

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Full Time Deviation Investigator information

See salary details

$32K

$75.3K

$131K

How much do full time deviation investigator jobs pay per year?

As of Jul 16, 2026, the average yearly pay for full time 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 are the key skills and qualifications needed to thrive as a Full Time Deviation Investigator, and why are they important?

To thrive as a Full Time Deviation Investigator, you need a solid background in life sciences, quality assurance, or pharmaceutical manufacturing, often supported by a relevant degree and experience with regulatory standards like GMP. Familiarity with investigation tools, root cause analysis methodologies (such as 5 Whys or Fishbone), and documentation systems is typically required. Strong analytical thinking, attention to detail, and effective communication skills help in identifying issues and collaborating across teams. These skills are crucial for ensuring regulatory compliance, maintaining product quality, and preventing future deviations in highly regulated environments.

What is the difference between Full Time Deviation Investigator vs Part Time Deviation Investigator?

AspectFull Time Deviation InvestigatorPart Time Deviation Investigator
Work HoursTypically 40 hours/week, full-time scheduleFewer hours, part-time schedule
CertificationsOften requires similar certifications, such as compliance or industry-specific licensesMay require the same certifications but with less emphasis on full-time status
Work EnvironmentOffice-based, field visits, and investigationsSimilar environment but with flexible or reduced hours
Employer UsageCommonly employed by insurance companies, healthcare, or regulatory agenciesUsed by organizations needing flexible investigation support

Full Time Deviation Investigators work standard hours and are employed full-time, often with comprehensive benefits. Part Time Deviation Investigators work fewer hours, offering flexibility but potentially fewer benefits. Both roles require similar skills and certifications, but the employment structure differs based on organizational needs.

What does a Full Time Deviation Investigator do?

A Full Time Deviation Investigator is responsible for investigating deviations from standard operating procedures, quality standards, or regulations in industries such as pharmaceuticals, manufacturing, or food production. Their main role is to identify the root cause of deviations, document findings, and recommend corrective and preventive actions to ensure compliance and product quality. They work closely with quality assurance, production, and regulatory teams to resolve issues efficiently and maintain high standards. This position requires strong analytical, problem-solving, and communication skills, as well as knowledge of relevant regulatory guidelines.

What are the main challenges Full Time Deviation Investigators face when managing multiple investigations simultaneously?

Full Time Deviation Investigators often juggle several investigations at once, which requires strong organizational and time management skills. Prioritizing cases based on risk and regulatory deadlines can be challenging, especially in high-compliance environments like pharmaceuticals or manufacturing. Investigators must also coordinate with cross-functional teams, such as Quality Assurance, Production, and Engineering, to gather accurate information and implement corrective actions promptly. Balancing thoroughness with efficiency is key to ensuring all deviations are properly addressed without causing workflow bottlenecks.
More about Full Time Deviation Investigator jobs
What cities are hiring for Full Time Deviation Investigator jobs? Cities with the most Full Time Deviation Investigator job openings:
What are the most commonly searched types of Deviation Investigator jobs? The most popular types of Deviation Investigator jobs are:
What states have the most Full Time Deviation Investigator jobs? States with the most job openings for Full Time Deviation Investigator jobs include:
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Infographic showing various Full Time Deviation Investigator job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $75,325 per year, or $36.2 per hour.
Deviation Investigation Specialist

Deviation Investigation Specialist

Praxis Packaging

Grand Rapids, MI

$55K - $75K/yr

Full-time

Posted 4 days ago


Job description

Overview

Join a critical role at the intersection of quality, compliance, and operations. As a Deviation Investigation Specialist, you'll lead root cause investigations, develop clear and compliant technical documentation, and partner with cross-functional teams to drive continuous improvement in a fast-paced contract packaging manufacturing environment.

 Responsibilities
  • Investigates deviations related to Primary Production.  
  • Facilitates TW change controls related to Primary Production.
  • Serves as backup to the Primary Production manager in any TW related meetings or cases.
  • Assists with management of assigned projects. 
  • Ensures projects are completed by established deadlines.
  • Contributes as subject matter expert (SME) in applicable projects related to Primary Production.
  • Adherence to all Company policies and procedures.
  • Works to improve the effectiveness of the quality management system through the use of the quality policy, quality objectives, audit results, analysis of data, corrective and preventive actions.
  • Provides assistance and answers a diverse workforce of 5-10 employees.
  • Instills a sense of quality through modeled quality behaviors and mindset.
  • Assists with Training and Orientation.
  • Ensures employees are trained according to their roles.
  • Elevates complaints and problems, seeks Management assistance.
  • Ensures proper PPE's and Safety procedures are followed.
Qualifications
  • High school diploma or equivalent required.
  • Associates Degree or equivalent combination preferred.
  • 2-4 years plus similar experience required.
  • Strong GDP/GMP experience required.
  • Lead/Group Leader experience preferred.
  • Basic Mechanical and mathematical aptitude required.
  • The ability to work independently, without supervision required.
  • Ability to organize priorities and workload required.
Pay RangeUSD $55,000.00 - USD $75,000.00 /Yr.Employment Type: FULL_TIME