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Full Time Deviation Investigator Jobs (NOW HIRING)

Union Agener

API Operations Manager

Augusta, GA · On-site

API Operations Manager Supervisor Title : Sr. Manufacturing Manager Position Type : Full Time ... Submit, investigate, and approve deviation investigations and change controls. * Maintain ...

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Full Time Deviation Investigator information

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$32K

$75.3K

$131K

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

As of Jul 17, 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:
What job categories do people searching Full Time Deviation Investigator jobs look for? The top searched job categories for Full Time Deviation Investigator jobs are:
Full Time Deviation Investigator jobs near you
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.
Automation Engineer

Automation Engineer

Quality Agents, LLC

Rockville, MD

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.
We are seeking a hands-on and detail-driven Automation Engineer to support the design, implementation, and maintenance of automation systems in a regulated biotech manufacturing environment. This role will play a key part in optimizing equipment performance, ensuring data integrity, and maintaining GMP compliance across automated systems.
The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process automation in GMP settings.


Key Responsibilities


Support automation projects related to manufacturing, utilities, and lab systems (e.g., bioreactors, chromatography skids, CIP/SIP systems).
Develop, modify, and troubleshoot automation logic (PLC, SCADA, DCS) in support of process control and equipment integration.
Work closely with cross-functional teams on system requirements, design specifications, and commissioning/qualification (IQ/OQ/PQ) activities.
Maintain and update automation-related documentation including functional specs, FRS, URS, and validation protocols.
Ensure compliance with 21 CFR Part 11, data integrity, GAMP5, and other relevant GMP regulations.
Collaborate with QA, Validation, Engineering, and IT to support system lifecycle management and change control.
Support deviation investigations, CAPAs, and root cause analysis for automation-related issues


Minimum Requirements:


B.S. in Electrical Engineering, Chemical Engineering, Computer Science, or a related field.
3+ years of experience in automation engineering within a biotech, pharmaceutical, or GMP-regulated environment.
Experience with automation platforms such as Allen-Bradley, Siemens, DeltaV, Rockwell, Wonderware/AVEVA, or similar.
Strong understanding of control systems, instrumentation, and network infrastructure in GMP settings.
Familiarity with automation validation and documentation standards.


Quality Agents offers a full suite of benefits for full-time employees including:


Health, dental and vision insurance
Life, AD&D and Disability Insurance
Health savings account for participants in our health plan
401k retirement plan
Paid time off
Paid holidays


Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.

Apply