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From Home Deviation Investigator Jobs (NOW HIRING)

Amgen

Sr Associate Mfg I- Investigations

Holly Springs, NC · On-site

$13 - $15.50/hr

Manage simple deviation and environmental monitoring investigations, specifically within the ... From our competitive benefits to our collaborative culture, we'll support your journey every step ...

VRC Investigations

SIU Investigator

New York, NY · On-site

$30 - $35/hr

We have several work from home, part-time and full-time hourly positions available in our rapidly expanding Special Investigations Unit. This work from home position requires travel within the ...

Actalent

Quality Investigator

Raleigh, NC

$45 - $50/hr

Support external audits from regulatory agencies and customers, including roles such as Document ... Proficiency in deviation investigations, root cause analysis, and GMP compliance. * Proven ability ...

VRC Investigations

SIU Investigator

Queens, NY · On-site

$30 - $35/hr

We have several work from home, part-time and full-time hourly positions available in our rapidly expanding Special Investigations Unit. This work from home position requires travel within the ...

Actalent

Quality Investigator

Raleigh, NC

$45 - $50/hr

Support external audits from regulatory agencies and customers, including roles such as Document ... Proficiency in deviation investigations, root cause analysis, and GMP compliance. * Proven ability ...

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From Home Deviation Investigator information

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How much do from home deviation investigator jobs pay per year?

As of Aug 12, 2026, the average yearly pay for from home 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 is the difference between From Home Deviation Investigator vs From Home Quality Assurance Specialist?

AspectFrom Home Deviation InvestigatorFrom Home Quality Assurance Specialist
Required CredentialsTypically requires a background in healthcare, nursing, or pharmacy, with certifications in quality or complianceOften requires similar healthcare or industry-specific certifications, with additional quality assurance training
Work EnvironmentPrimarily remote, investigating deviations or compliance issues in clinical or pharmaceutical settingsPrimarily remote, focusing on monitoring and improving quality processes across products or services
Employer & Industry UsageUsed mainly in pharmaceutical, healthcare, and clinical research industriesCommon in healthcare, manufacturing, and service industries

Both roles are remote and require healthcare or quality-related certifications. The main difference lies in their focus: Deviation Investigators handle compliance deviations, while Quality Assurance Specialists focus on overall quality improvement. Both roles are essential for maintaining industry standards but serve different functions within organizations.

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From Home Deviation Investigator jobs near you
Infographic showing various From Home Deviation Investigator job openings in the United States as of August 2026, with employment types broken down into 52% Full Time, 8% Part Time, 36% Contract, and 4% Nights. Highlights an 88% In-person, and 12% Remote job distribution, with an average salary of $75,325 per year, or $36.2 per hour.

Deviation Specialist II

Thermo Fisher Scientific

Greenville, NC • On-site

Full-time

Re-posted 4 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 423 frontline employees who took The Breakroom Quiz

200th of 538 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
A leading pharmaceutical organization is seeking a Deviation Specialist to support its quality and compliance operations within a high-volume sterile manufacturing facility. This role focuses on conducting thorough investigations, driving root cause analysis, and contributing to continuous improvement initiatives in a regulated environment. This role ensures that all deviations are managed in compliance with company policies and industry regulations, and that corrective and preventive actions (CAPAs) are implemented effectively. The ideal candidate will be a skilled technical writer with strong communication and problem-solving abilities, and a comfort level in navigating complex production environments.
Key Responsibilities:
Deviation Management:
  • Identify and document deviations from standard operating procedures (SOPs), quality standards, or regulatory guidelines.
  • Conduct thorough investigations to determine the root cause of deviations.
  • Collaborate with cross-functional teams to develop and implement corrective and preventive actions (CAPAs).

Documentation and Reporting:
  • Maintain accurate and detailed records of all deviations, investigations, and CAPAs.
  • Prepare and present deviation reports to management and regulatory authorities as required.
  • Ensure documentation is completed in accordance with Good Documentation Practices (GDP).

Compliance and Quality Assurance:
  • Ensure all deviations are managed in compliance with company policies, industry standards, and regulatory requirements.
  • Participate in internal and external audits and inspections, providing necessary documentation and information related to deviations.

Continuous Improvement:
  • Analyze deviation trends and provide insights for continuous improvement initiatives.
  • Participate in training programs to enhance knowledge and skills related to deviation management and quality assurance.

Qualifications:
  • Regulated Industry, cGMP environment experience, deviation management, or a e.g., Pharmaceuticals, Manufacturing, Engineering, Medical, Law Enforcement, etc.].
  • Strong Attention to details, technical writing, Analytical and problem-solving skills.
  • Knowledge of regulatory requirements and standards.
  • Intermediate to Advanced skills in Microsoft Suite (Word, Excel, PowerPoint)
  • Excellent communication and interpersonal skills.

Preferred Qualifications:
  • Associate or bachelor's degree in a relevant field such as Life Sciences, Engineering, Medial, or Quality Management with 2+ years of related experience.
  • Preferred Experience: Biologics, Aseptic, Filling Isolators, Six Sigma Certification, Electronic documentation systems.
  • Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

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