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Full Time Deviation Investigator Jobs (NOW HIRING)

Participate in deviation/incident investigations; perform root cause analysis and implement ... Schedule : Full-time * May require additional availability or flexibility for audits or ...

Manufacturing Engineer I

Hollister, CA ยท On-site

$75K - $88K/yr

Job Type Full-time Description Join the Teknova Team and Help Shape the Future of Health When you ... Participate in deviation investigations, CAPA activities, nonconformance reviews, and process ...

Serve as subject matter expert in CAPA and deviation investigations, using root cause analysis and ... Vacation time from day one * 9 paid holidays for regular full-time employees * Paid training

Manufacturing Supervisor

Fishers, IN ยท On-site

$56K - $77K/yr

Involvement in manufacturing deviation investigations and CAPA implementation. Influencing the ... Employment Type: Full-Time

Showing results 41-60

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 Aug 7, 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?

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:
Infographic showing various Full Time Deviation Investigator job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $75,325 per year, or $36.2 per hour.

Downstream Manufacturing Scientist

Kashiv Biosciences LLC

Piscataway, NJ โ€ข On-site

$95K/yr

Full-time

Re-posted 6 days ago


Job description

Job Type
Full-time
Description
Downstream Manufacturing Scientist (Piscataway, NJ): Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis; provide technical direction in the execution and development of the purification process; use programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments, or equipment as well as prepares / reviews all quality management related documents (Deviation / Change control/investigation reports etc.). Base Salary: $95,000 per year.
Requirements
Req's Master's degree (or foreign equivalent degree) in Molecular and Cell Biology or a related field, with knowledge of at least 5 skills from the following list: process development, cGMP Manufacturing MSAT, Bacterial & Mammalian Cell Culture, Depth Filtration, Quality Management Systems, Downstream Purification & Analytical Chromatography.
Apply to HR at Kashiv BioSciences LLC, 20 New England Avenue, Piscataway, NJ 08854.