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From Home Deviation Investigator Jobs (NOW HIRING)

Catalent, Inc.

Site Deviation Investigator

Greendale, IN · On-site

  • Medical

  • Dental

  • Vision

  • PTO

Gather information from internal and external sources to evaluate deviation impact on products and ... Present completed investigations to the site leadership team for concurrence. * Keep site ...

Lonza

Deviation Investigation Level 2 - Night Shift

Portsmouth, NH · On-site

$22 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Deviation Investigator II is responsible for leading and executing deviation investigations ... Support and contribute to major deviation investigations with guidance from team leadership

Lonza

Deviation Investigation Level 2 - Night Shift

Portsmouth, NH · On-site

$22 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Deviation Investigator II is responsible for leading and executing deviation investigations ... Support and contribute to major deviation investigations with guidance from team leadership

TekWissen LLC

Quality Records Investigator

Houston, TX · On-site

$20 - $24/hr

Monday to Friday from 08:00 AM to 05:00 PM Summary The Deviation Investigator/Initiator is responsible for initiating, investigating, and completing Minor and low/medium severity Major process ...

Medasource

GMP Compliance Investigator

Durham, NC · On-site

Manage deviation, CAPA, and change control timelines to support on-time batch release. * Perform failure mode analysis and root cause investigations. * Support batch release activities from a ...

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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 13, 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.

Manufacturing Deviation Investigator

TekWissen LLC

Houston, TX • On-site

$20 - $24/wk

Contractor

Re-posted 13 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:       Manufacturing Deviation Investigator / Sr. Quality Records Investigator
Location:       Houston, TX - 77047
Duration:       6 Months    
Job Type:       Contract    
Work Type:   Onsite 
 Shift:             Monday to Friday - 08:00 AM to 05:00 PM
 
 
Summary
 
The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.
 
 
Responsibilities
  • Technical writing for the educated but uninformed reader, translate difficult and complex scientific events into a brief and cohesive report as a finished product.
  • Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report.
  • Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.
  • Management of multiple projects and timelines concurrently.
  • Ability to adhere to standard timeline, and escalate actions appropriately for resolution in a timely manner.
  • Participation in the Daily Management meetings to update leadership or current deviation statuses.
  • Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.
  • Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews.
  • Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward.
  • Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty.
  • Attendance and occasional leadership of the daily management system and participating/leading the deviation review board.
  • Perform other duties as assigned. 
Required Skills 
  • Prior experience in Technical writing and documentation
  • Prior experience in performing in Deviation investigation and root cause analysis (RCA)
  • Strong hands on experience with CAPA (Corrective and Preventive Actions) creation and follow-through
  • Understanding of cGMP and pharmaceutical/biotech manufacturing
  • Quality systems and deviation lifecycle management
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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